836-35-1 Usage
Description
2-(3-TRIFLUOROMETHYL-PHENOXY)-PROPIONIC ACID, also known as 2-(3-trifluoromethylphenoxy)propanoic acid, is a chemical compound that belongs to the class of propionic acids. It is characterized by the presence of a trifluoromethyl group attached to a phenoxy moiety, which is connected to a propionic acid chain. This unique molecular structure endows the compound with specific chemical properties and reactivity, making it a versatile building block in the synthesis of various organic compounds.
Uses
Used in Pharmaceutical Industry:
2-(3-TRIFLUOROMETHYL-PHENOXY)-PROPIONIC ACID is used as an active pharmaceutical ingredient for its anti-inflammatory properties. It is incorporated into pharmaceutical products to help alleviate inflammation and associated symptoms, providing therapeutic benefits to patients.
Used in Agrochemical Industry:
In the agricultural sector, 2-(3-TRIFLUOROMETHYL-PHENOXY)-PROPIONIC ACID is utilized as a herbicide. Its application helps control and eliminate unwanted plant growth, thereby improving crop yields and ensuring the efficient use of agricultural resources.
Used as a Building Block in Organic Synthesis:
Due to its unique molecular structure, 2-(3-TRIFLUOROMETHYL-PHENOXY)-PROPIONIC ACID serves as a valuable building block in the synthesis of other organic compounds. Its reactivity and the presence of the trifluoromethyl group make it particularly useful in certain chemical reactions, contributing to the development of new and innovative chemical products.
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.
