Yamaoka, Hidenori et al. published their research in Organic Process Research & Development in 2004 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Electric Literature of C12H20O6

A practical RuCl3-catalyzed oxidation using trichloroisocyanuric acid as a stoichiometric oxidant under mild nonacidic conditions was written by Yamaoka, Hidenori;Moriya, Narimasa;Ikunaka, Masaya. And the article was included in Organic Process Research & Development in 2004.Electric Literature of C12H20O6 This article mentions the following:

The combined use of catalytic RuCl3 and stoichiometric trichloroisocyanuric acid in the presence of n-Bu4NBr and K2CO3 allowed smooth oxidation of primary alcs. to carboxylic acids. Secondary alcs. can be oxidized to ketones when using the same set of the reagents. By proceeding under the nonacidic biphasic conditions dispensing with hazardous reagents, the oxidation reactions were applicable to structurally diverse alcs., easy to work up, environmentally benign, and basically high-yielding. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Electric Literature of C12H20O6).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Electric Literature of C12H20O6

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Hajlaoui, Khaoula et al. published their research in Journal of Heterocyclic Chemistry in 2018 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.COA of Formula: C12H20O6

Synthesis of Novel Pyrazole-sucrose Derivatives by 1,3-dipolar Cycloaddition was written by Hajlaoui, Khaoula;El Guesmi, Ahlem;Ben Hamadi, Naoufel;Msaddek, Moncef. And the article was included in Journal of Heterocyclic Chemistry in 2018.COA of Formula: C12H20O6 This article mentions the following:

The syntheses of an important class of enantiopure five-membered glycoconjugates containing furan unit are described. The regioselective synthesis of a series of sugar-fused pyrazole heterocycles was achieved by the Huisgen cyclization of aryl diazomethanes with propargyl O-glycoside derivatives in good yields. The cycloaddition regioselectivity was confirmed by NMR. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1COA of Formula: C12H20O6).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.COA of Formula: C12H20O6

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Liu, Jun et al. published their research in Science China: Chemistry in 2013 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

Total synthesis of (-)-isoaltholactone was written by Liu, Jun;Zhang, Xing;Liu, Yi;Bi, JingJing;Du, YuGuo. And the article was included in Science China: Chemistry in 2013.Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol This article mentions the following:

A short and efficient stereoselective synthesis of a styryllactone (-)-isoaltholactone, I, has been achieved in seven steps and 33% overall yield, starting from the readily available carbohydrate D-mannose. The key steps of our synthesis involve intramol. THF cyclization and one-pot acetonide deprotection-lactonization. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Van Boggelen, Michel P. et al. published their research in Tetrahedron in 1997 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

Methyl iodide mediated cleavage of the nitrogen-oxygen bond of isoxazolidines was written by Van Boggelen, Michel P.;Van Dommelen, Bart F. G. A.;Jiang, Shende;Singh, Gurdial. And the article was included in Tetrahedron in 1997.Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol This article mentions the following:

A novel method of N-O bond cleavage in isoxazolidines is described. Treatment of isoxazolidine with excess of Me iodide in THF under reflux gave the quaternary ammonium iodide alc. and the α,β-unsaturated aldehyde. The former can be converted to the latter via the Swern oxidation In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Name: (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Carro, Carmen et al. published their research in European Journal of Organic Chemistry in 2017 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Recommanded Product: 14131-84-1

Microwave versus Conventional Light Activation of O-Radical Scission Processes was written by Carro, Carmen;Romero, Ivan;Boto, Alicia. And the article was included in European Journal of Organic Chemistry in 2017.Recommanded Product: 14131-84-1 This article mentions the following:

Domino or sequential processes initiated by cleavage of O radicals has led to the conversion of low-cost, readily available substrates into high-profit products. The optimization of these processes by using different activation sources (irradiation with visible light, microwaves, and conventional heating) is described herein, as well as their application to the conversion of carbohydrates, amino acids, peptides, and terpenes into valuable derivatives In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Recommanded Product: 14131-84-1).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Recommanded Product: 14131-84-1

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Dondoni, Alessandro et al. published their research in Chemistry – A European Journal in 1997 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Recommanded Product: 14131-84-1

Synthesis and properties of O-glycosyl calix[4]arenes (calixsugars) was written by Dondoni, Alessandro;Marra, Alberto;Scherrmann, Marie-Christine;Casnati, Alessandro;Sansone, Francesco;Ungaro, Rocco. And the article was included in Chemistry – A European Journal in 1997.Recommanded Product: 14131-84-1 This article mentions the following:

Model O-glycosylation reactions at either rim of calix[4]arenes are described with the aim of providing access to a new family of carbohydrate-containing calixarene derivatives named calixsugars. One or two sugar moieties (D-mannofuranose and D-glucopyranose) were introduced at the lower rim of the parent calix[4]arene by glycosylation of the phenolic hydroxyl groups by means of a Mitsunobu reaction. Tetrapropoxy calix[4]-arenes bearing two or four hydroxymethyl groups at the upper rim were coupled with perbenzoylated thioethyl D-galactoside and D-lactoside in the presence of the thiophilic promoter copper(II) triflate. In this way β-linked bis- and tetrakis-O-galactosyl calix[4]arenes were obtained in good yield, the latter showing some solubility in water. For the O-lactosyl derivatives only the bis-substituted compound could be obtained because of the competing formation of an intramol. ether linkage between 1,3-hydroxymethyl groups. Preliminary binding studies showed some affinity of the galactose-containing calixsugars toward charged carbohydrates and dihydrogen phosphate anion. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Recommanded Product: 14131-84-1).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Recommanded Product: 14131-84-1

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Yamaoka, Hidenori et al. published their research in Organic Process Research & Development in 2004 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Electric Literature of C12H20O6

A practical RuCl3-catalyzed oxidation using trichloroisocyanuric acid as a stoichiometric oxidant under mild nonacidic conditions was written by Yamaoka, Hidenori;Moriya, Narimasa;Ikunaka, Masaya. And the article was included in Organic Process Research & Development in 2004.Electric Literature of C12H20O6 This article mentions the following:

The combined use of catalytic RuCl3 and stoichiometric trichloroisocyanuric acid in the presence of n-Bu4NBr and K2CO3 allowed smooth oxidation of primary alcs. to carboxylic acids. Secondary alcs. can be oxidized to ketones when using the same set of the reagents. By proceeding under the nonacidic biphasic conditions dispensing with hazardous reagents, the oxidation reactions were applicable to structurally diverse alcs., easy to work up, environmentally benign, and basically high-yielding. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Electric Literature of C12H20O6).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Electric Literature of C12H20O6

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Hajlaoui, Khaoula et al. published their research in Journal of Heterocyclic Chemistry in 2018 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.COA of Formula: C12H20O6

Synthesis of Novel Pyrazole-sucrose Derivatives by 1,3-dipolar Cycloaddition was written by Hajlaoui, Khaoula;El Guesmi, Ahlem;Ben Hamadi, Naoufel;Msaddek, Moncef. And the article was included in Journal of Heterocyclic Chemistry in 2018.COA of Formula: C12H20O6 This article mentions the following:

The syntheses of an important class of enantiopure five-membered glycoconjugates containing furan unit are described. The regioselective synthesis of a series of sugar-fused pyrazole heterocycles was achieved by the Huisgen cyclization of aryl diazomethanes with propargyl O-glycoside derivatives in good yields. The cycloaddition regioselectivity was confirmed by NMR. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1COA of Formula: C12H20O6).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.COA of Formula: C12H20O6

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Chen, Fen-Er et al. published their research in Carbohydrate Research in 2007 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Application In Synthesis of (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

An improved synthesis of a key intermediate for (+)-biotin from D-mannose was written by Chen, Fen-Er;Zhao, Jian-Feng;Xiong, Fang-Jun;Xie, Bin;Zhang, Ping. And the article was included in Carbohydrate Research in 2007.Application In Synthesis of (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol This article mentions the following:

An efficient and reproducible process for the synthesis of Me tetradeoxy-isopropylidene-D-arabinonanonate I, a key intermediate in the total synthesis of (+)-biotin II, starting from readily available D-mannose is described. The crucial part of this synthesis was the development of a practical route to a novel O-benzyl protected unsaturated ester Me (benzyl 5,6,7,8-tetradeoxy-2,3-O-isopropylidene-α-D-lyxo-nona-5,7-dienofuranosid) uronate, allowing the one-step preparation of hydroxy ester Me 5,6,7,8-tetradeoxy-2,3-O-isopropylidene-α-D-lyxo-nanofuranuronate by the catalytic debenzylation and hydrogenation over palladium on carbon catalyst. This procedure requires no chromatog. purification, which makes it ideal for synthetic preparation on an industrial scale. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Application In Synthesis of (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Application In Synthesis of (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem

Wang, Xiao et al. published their research in Polymer Chemistry in 2014 | CAS: 14131-84-1

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Formula: C12H20O6

Monosaccharide-functionalized poly(phenylacetylenes): in situ polymerization, hybridization with MWCNTs, and application in the reinforcement of chitosan rods was written by Wang, Xiao;Gao, Yuan;Zhao, Hui;Liu, Xiao-Qing;Wang, Zhengke;Qin, Anjun;Hu, Qiaoling;Sun, Jing Zhi;Tang, Ben Zhong. And the article was included in Polymer Chemistry in 2014.Formula: C12H20O6 This article mentions the following:

Monosaccharide-functionalized poly(phenylacetylenes) (PPAs) are synthesized with high yield and mol. weight, but it shows no solvating power to multi-walled carbon nanotubes (MWCNTs) by simply blending them together. Polymerization of monosaccharide-functionalized monomers in the presence of MWCNTs (in situ polymerization) leads to the hybrids of monosaccharide-functionalized PPAs/MWCNTs, and the content of MWCNTs is over 2% by weight The characterization data indicates that the π-π interaction between the styrene-like moieties in the polymer backbone and the MWCNTs plays crucial role in the dispersing capacity. Based on the in situ precipitation method, CS rods containing monosaccharide-functionalized PPAs/MWCNTs hybrids were fabricated. The bending strength and modulus of the hybrid-reinforced CS rods showed substantial improvement in comparison with the CS rods made from pristine and hydroxyapatite-reinforced CS. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1Formula: C12H20O6).

(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.Formula: C12H20O6

Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem