836-35-1 Usage
General Description
2-(3-trifluoromethyl-phenoxy)-propionic acid is a chemical compound that belongs to the class of propionic acids. It is also known by the chemical name 2-(3-trifluoromethylphenoxy)propanoic acid. 2-(3-TRIFLUOROMETHYL-PHENOXY)-PROPIONIC ACID is used in the production of pharmaceuticals and agrochemicals. It is known for its anti-inflammatory properties and is used as an active ingredient in some pharmaceutical products. Additionally, it is used as a herbicide in the agricultural industry. The presence of the trifluoromethyl group in its molecular structure makes this compound particularly useful in certain chemical reactions and as a building block for the synthesis of other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 836-35-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 836-35:
(5*8)+(4*3)+(3*6)+(2*3)+(1*5)=81
81 % 10 = 1
So 836-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F3O3/c1-6(9(14)15)16-8-4-2-3-7(5-8)10(11,12)13/h2-6H,1H3,(H,14,15)
836-35-1Relevant articles and documents
Access to Optically Enriched α-Aryloxycarboxylic Esters via Carbene-Catalyzed Dynamic Kinetic Resolution and Transesterification
Liu, Bin,Song, Runjiang,Xu, Jun,Majhi, Pankaj Kumar,Yang, Xing,Yang, Song,Jin, Zhichao,Chi, Yonggui Robin
supporting information, p. 3335 - 3338 (2020/04/30)
Optically active α-aryloxycarboxylic acids and their derivatives are important functional molecules. Disclosed here is a carbene-catalyzed dynamic kinetic resolution and transesterification reaction for access to this class of molecules with up to 99% yields and 99:1 er values. Addition of a chiral carbene catalyst to the ester substrate leads to two diastereomeric azolium ester intermediates that can quickly epimerize to each other and thus allows for effective dynamic kinetic resolution to be realized. The optically enriched ester products from our reaction can be quickly transformed to chiral herbicides and other bioactive molecules.
