32190-82-2 Usage
Description
(2R)-2-methylbicyclo[2.2.1]hept-5-ene-2-carboxylic acid, also known as bornylacetic acid, is a chemical compound with a bicyclic structure and a carboxylic acid functional group. It is commonly found in essential oils, particularly in the oil of pine trees.
Uses
Used in Flavoring Agents:
(2R)-2-methylbicyclo[2.2.1]hept-5-ene-2-carboxylic acid is used as a flavoring agent in the food and beverage industry due to its unique aroma and taste.
Used in Antimicrobial Applications:
(2R)-2-methylbicyclo[2.2.1]hept-5-ene-2-carboxylic acid is used as an antimicrobial agent for its ability to inhibit the growth of certain bacteria and fungi.
Used in Anti-inflammatory Applications:
(2R)-2-methylbicyclo[2.2.1]hept-5-ene-2-carboxylic acid is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate pain.
Used in Research and Development:
(2R)-2-methylbicyclo[2.2.1]hept-5-ene-2-carboxylic acid is used as a target for further research and potential applications in various fields due to its unique structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 32190-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,9 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32190-82:
(7*3)+(6*2)+(5*1)+(4*9)+(3*0)+(2*8)+(1*2)=92
92 % 10 = 2
So 32190-82-2 is a valid CAS Registry Number.
32190-82-2Relevant articles and documents
Broadly Applicable Ytterbium-Catalyzed Esterification, Hydrolysis, and Amidation of Imides
Guissart, Céline,Barros, Andre,Rosa Barata, Luis,Evano, Gwilherm
supporting information, p. 5098 - 5102 (2018/09/13)
An efficient, broadly applicable, operationally simple, and divergent process for the transformation of imides into a range of carboxylic acid derivatives under mild conditions is reported. By simply using catalytic amounts of ytterbium(III) triflate as a Lewis acid promoter in the presence of alcohols, water, amines, or N,O-dimethylhydroxylamine, a broad range of imides is smoothly and readily converted to the corresponding esters, carboxylic acids, amides, and Weinreb amides in good yields. This method notably enables an easy cleavage of oxazolidinone-based auxiliaries.
