New research progress on 114214-49-2 in 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. In an article, author is Banwell, Martin G., once mentioned the application of 114214-49-2, Synthetic Route of 114214-49-2, Name is tert-Butyl 6-oxa-3-azabicyclo[3.1.0]hexane-3-carboxylate, molecular formula is C9H15NO3, molecular weight is 185.22, MDL number is MFCD08691407, category is dioxole. Now introduce a scientific discovery about this category.
(2R,3aS,5aR,8aR,8bS)-4-Bromo-2-(4methoxyphenyl)-7,7-dimethyl-3a,5a,8a,8b-tetrahydrobenzo[1,2-d:3,4-d ‘]bis[1,3]dioxole
The title compound, C17H19BrO5, bears an exo-orientated or R-configured 4-methoxyphenyl group and incorporates a C – O bond that is distinctly shorter than the three remaining acetal C – O bonds [1.415 (4) versus 1.431 (4) – 1.448 (4) angstrom and 1.421 (4) versus 1.436 (4) – 1.448 (4) angstrom for the two molecules in the asymmetric unit].
Synthetic Route of 114214-49-2, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 114214-49-2.
Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem