Category: 25150-27-0

Quality Control of 6,7-Dichlorobenzo[d]thiazol-2-amine. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about Hetarylazo disperse dyes derived from 5,6-dichloro- and 6,7-dichloro-2-aminobenzothiazoles. Author is Peters, A. T.; Tsatsaroni, E.; Ma, Xisai.

The isomer mixtures resulting from the diazotization of 5,6-(6,7-)dichloro-2-aminobenzothiazole and coupling to N-substituted anilines were separable by column chromatog. Isomer characterization was effected by unambiguous dye synthesis from the individual dichloro-2-aminobenzothiazoles, and by 1H NMR. The color and dyeing parameters of the isomers on polyester were essentially equivalent, and similar to those of the corresponding isomer mixtures

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

Application of 25150-27-0. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about Synthesis, characterization and biological activity of 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-phenyl-3,5-dihydro-4H-imidazol-4-ones. Author is Baldaniya, B. B..

Some novel 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-2-phenyl-3,5-dihydro-4H-imidazol-4-ones were synthesized and characterized by elemental analyses, IR, NMR, and mass spectra. The products were evaluated for antibacterial and antifungal activities against different strains of bacteria and fungi.

From this literature《Synthesis, characterization and biological activity of 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-phenyl-3,5-dihydro-4H-imidazol-4-ones》,we know some information about this compound(25150-27-0)Application of 25150-27-0, but this is not all information, there are many literatures related to this compound(25150-27-0).

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

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine( cas:25150-27-0 ) is researched.Name: 6,7-Dichlorobenzo[d]thiazol-2-amine.Baldaniya, B. B. published the article 《Synthesis, characterization and biological activity of 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-phenyl-3,5-dihydro-4H-imidazol-4-ones》 about this compound( cas:25150-27-0 ) in E-Journal of Chemistry. Keywords: arylidene oxazolone condensation benzothiazolamine; imidazolone arylidene benzothiazolyl preparation antibacterial antifungal activity. Let’s learn more about this compound (cas:25150-27-0).

Some novel 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-2-phenyl-3,5-dihydro-4H-imidazol-4-ones were synthesized and characterized by elemental analyses, IR, NMR, and mass spectra. The products were evaluated for antibacterial and antifungal activities against different strains of bacteria and fungi.

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

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about Synthesis, characterization and antibacterial activity of 3-(6,7 substituted-1,3-benzothiazol-2-yl)-4-(4-substituted phenyl)-1,3-thiazolidin-2-one derivatives.Electric Literature of C7H4Cl2N2S.

Disubstituted 2-aminobenzothiazole derivatives (2) have been prepared from disubstituted aniline (1) in presence of potassium thiocynate, bromine, glacial acetic acid and ammonia solution It has been reacted with various aromatic aldehydes (3a-g) to afford Schiff’s base derivatives (4a-g). Further, these schiff’s bases are refluxed with thioglycolic acid in presence of DMF to afford 3-(6,7-substituted-1,3-benzothiazol-2-yl)-4-(4-substituted phenyl)-1,3-thiazolidin-2-one derivatives (5a-g, 6a-g, 7a-g, 8a-g, 9a-g, 10a-g). The title compounds and their derivatives have been characterized by their spectral data. The synthesized compounds were screened for their antibacterial activity against Staphylococcus aureus, Bacillus substilis, Escherichia coli and Pseudomonas aeruginosa.

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

COA of Formula: C7H4Cl2N2S. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about 5,6-(6,7-)dichlorobenzothiazolylazo dyes for synthetic polymer fibers. Author is Peters, A. T.; Gbadamosi, N. M. A..

The synthesis and properties of a series of monoazo dyes derived from an isomer mixture of 5,6-dichloro- and 6,7-dichloro-2-aminobenzothiazoles as the diazo component are reported. By appropriate selection of substituents in the coupling component, dyes varying in hue from orange-red to deep violet can be obtained. Coloration and light-fastness evaluations of the dyes on polyester fiber indicate that they can be viable alternatives to anthraquinone-based dyes of similar hue.

From this literature《5,6-(6,7-)dichlorobenzothiazolylazo dyes for synthetic polymer fibers》,we know some information about this compound(25150-27-0)COA of Formula: C7H4Cl2N2S, but this is not all information, there are many literatures related to this compound(25150-27-0).

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

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about Identification of a novel series of tetrahydrodibenzazocines as inhibitors of 17β-hydroxysteroid dehydrogenase type 3, the main research direction is SAR preparation androstenedione hydroxysteroid dehydrogenase tetrahydrodibenzazocine derivative.Formula: C7H4Cl2N2S.

A novel series of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) inhibitors has been identified. These inhibitors, based on a dibenzazocine core, exhibited picomolar to low nanomolar inhibition of 17β-HSD3 in cell-free enzymic as well as in cell-based transcriptional reporter assays.

There is still a lot of research devoted to this compound(SMILES：NC1=NC2=CC=C(Cl)C(Cl)=C2S1)Formula: C7H4Cl2N2S, and with the development of science, more effects of this compound(25150-27-0) can be discovered.

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

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about Identification of a novel series of tetrahydrodibenzazocines as inhibitors of 17β-hydroxysteroid dehydrogenase type 3, the main research direction is SAR preparation androstenedione hydroxysteroid dehydrogenase tetrahydrodibenzazocine derivative.Computed Properties of C7H4Cl2N2S.

A novel series of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) inhibitors has been identified. These inhibitors, based on a dibenzazocine core, exhibited picomolar to low nanomolar inhibition of 17β-HSD3 in cell-free enzymic as well as in cell-based transcriptional reporter assays.

There is still a lot of research devoted to this compound(SMILES：NC1=NC2=CC=C(Cl)C(Cl)=C2S1)Computed Properties of C7H4Cl2N2S, and with the development of science, more effects of this compound(25150-27-0) can be discovered.

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

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine( cas:25150-27-0 ) is researched.HPLC of Formula: 25150-27-0.Baldaniya, B. B. published the article 《Synthesis and characterizations of N2-(aryl)-N4,N6-bis(6,7-dichloro-1,3-benzothiazol-2-yl)-1,3,5-triazine-2,4,6-triamines as biological potent agents》 about this compound( cas:25150-27-0 ) in E-Journal of Chemistry. Keywords: cyanuric chloride condensation thiazolamine; thiazolyl cyanuric chloride preparation reaction aryl amine; arylamino chlorobenzothiazolylamino triazine preparation antibacterial antifungal activity. Let’s learn more about this compound (cas:25150-27-0).

Some novel N2-(aryl)-N4,N6-bis(6,7-dichloro-1,3-benzothiazol-2-yl)-1,3,5-triazine-2,4,6-triamines were synthesized and characterized by elemental analyses, IR, NMR, and mass spectra. The products were tested for their antibacterial activity against gram (+)ve and gram (-)ve bacteria and also on different strains of fungi. Introduction of -OH, -OCH3, -NO2, -Cl and -Br groups to the heterocyclic frame work enhanced antibacterial and antifungal activities.

There is still a lot of research devoted to this compound(SMILES：NC1=NC2=CC=C(Cl)C(Cl)=C2S1)HPLC of Formula: 25150-27-0, and with the development of science, more effects of this compound(25150-27-0) can be discovered.

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

Computed Properties of C7H4Cl2N2S. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 6,7-Dichlorobenzo[d]thiazol-2-amine, is researched, Molecular C7H4Cl2N2S, CAS is 25150-27-0, about Synthesis, characterization and biological activity of 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-phenyl-3,5-dihydro-4H-imidazol-4-ones. Author is Baldaniya, B. B..

Some novel 5-arylidene-3-(6,7-dichloro-1,3-benzothiazol-2-yl)-2-phenyl-3,5-dihydro-4H-imidazol-4-ones were synthesized and characterized by elemental analyses, IR, NMR, and mass spectra. The products were evaluated for antibacterial and antifungal activities against different strains of bacteria and fungi.

There is still a lot of research devoted to this compound(SMILES：NC1=NC2=CC=C(Cl)C(Cl)=C2S1)Computed Properties of C7H4Cl2N2S, and with the development of science, more effects of this compound(25150-27-0) can be discovered.

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

Alaimo, Robert J. published an article about the compound: 6,7-Dichlorobenzo[d]thiazol-2-amine( cas:25150-27-0,SMILESS:NC1=NC2=CC=C(Cl)C(Cl)=C2S1 ).Formula: C7H4Cl2N2S. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:25150-27-0) through the article.

A series of 8-substituted and 7,8-disubstituted-4-oxo-3-(4H-pyrimido[2,1-b]benzothiazole)carboxylic acids (I) and esters including a 9-aza analog were synthesized from substituted 2-aminobenzothiazoles and di-Et ethoxymethylenemalonate. No significant antiparasitic activity was detected.

If you want to learn more about this compound(6,7-Dichlorobenzo[d]thiazol-2-amine)Formula: C7H4Cl2N2S, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(25150-27-0).

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