37526-67-3 Usage
Uses
Used in Pharmaceutical Industry:
2-(TRIFLUOROMETHYLTHIO)BENZOIC ACI is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure contributes to the development of new drugs with specific therapeutic properties, enhancing the range of treatments available for different medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(TRIFLUOROMETHYLTHIO)BENZOIC ACI is utilized as a key component in the production of insecticides. Its strong inhibitory effects on the growth of certain pests and parasites make it a valuable asset in agricultural protection, helping to control and prevent infestations that can damage crops and reduce yields.
Used in Research Laboratories:
2-(TRIFLUOROMETHYLTHIO)BENZOIC ACI also serves as a crucial reagent in research laboratories, where it is employed in a variety of chemical reactions. Its versatility and reactivity make it an essential tool for scientists working on the development of new chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 37526-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37526-67:
(7*3)+(6*7)+(5*5)+(4*2)+(3*6)+(2*6)+(1*7)=133
133 % 10 = 3
So 37526-67-3 is a valid CAS Registry Number.
37526-67-3Relevant academic research and scientific papers
Trifluoromethylation of thiophenols and thiols with sodium trifluoromethanesulfinate and iodine pentoxide
Ma, Jing-Jing,Yi, Wen-Bin,Lu, Guo-Ping,Cai, Chun
, p. 417 - 421 (2016/02/03)
A selective and facile trifluoromethylation process for a wide range of thiophenols and thiols under metal free conditions has been developed using two simple and safe solids, sodium trifluoro-methanesulfinate and iodine pentoxide, via the radical process.
Process for preparing aryl trifluoromethylsulfides
-
, (2008/06/13)
Trifluoromethylthiocopper, formed in situ by the reaction of bis-(trifluoromethylthio)mercury with copper, reacts with aromatic bromides and iodides to give aryl trifluoromethyl sulfides.
