3823-40-3 Usage
Description
3-(TRIFLUOROMETHYLTHIO)PHENOL, also known as 3-(Trifluoromethylthio)phenol, is an organic compound characterized by the presence of a trifluoromethylthio group attached to a phenol molecule. 3-(TRIFLUOROMETHYLTHIO)PHENOL exhibits unique chemical properties due to the presence of the trifluoromethylthio group, which can be utilized in various chemical reactions and applications.
Uses
Used in Agricultural Industry:
3-(TRIFLUOROMETHYLTHIO)PHENOL is used as a reactant for the preparation of 2-azolyl-4-phenoxypyrimidines, which are highly active herbicides. These herbicides are effective in inhibiting carotenoid biosynthesis, a crucial process in plant growth and development. By disrupting this process, these herbicides can effectively control and eliminate unwanted plant species in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 3823-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,2 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3823-40:
(6*3)+(5*8)+(4*2)+(3*3)+(2*4)+(1*0)=83
83 % 10 = 3
So 3823-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F3OS/c8-7(9,10)12-6-3-1-2-5(11)4-6/h1-4,11H
3823-40-3Relevant articles and documents
Gold (I/III)-Catalyzed Trifluoromethylthiolation and Trifluoromethylselenolation of Organohalides
Mudshinge, Sagar R.,Yang, Yuhao,Xu, Bo,Hammond, Gerald B.,Lu, Zhichao
supporting information, (2022/02/10)
The first C?SCF3/SeCF3 cross-coupling reactions using gold redox catalysis [(MeDalphos)AuCl], AgSCF3 or Me4NSeCF3, and organohalides as substrates are reported. The new methodology enables a one-stop shop synthesis of aryl/alkenyl/alkynyl trifluoromethylthio- and selenoethers with a broad substrate scope (>60 examples with up to 97 % isolated yield). The method is scalable, and its robustness is evidenced by the late-stage functionalization of various bioactive molecules, which makes this reaction an attractive alternative in the synthesis of trifluoromethylthio- and selenoethers for pharmaceutical and agrochemical research and development.