57830-48-5 Usage
General Description
2-(Trifluoromethylthio)benzaldehyde is a chemical compound with the molecular formula C8H5F3OS. It is a yellow liquid with a strong odor and is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2-(TRIFLUOROMETHYLTHIO)BENZALDEHYDE is also used as a flavoring agent in the food industry. Its trifluoromethyl group makes it highly reactive, allowing it to participate in various chemical reactions, including oxidation and reduction reactions. It is important to handle 2-(trifluoromethylthio)benzaldehyde with caution, as it can be harmful if ingested or inhaled and may cause irritation to the skin and eyes upon contact.
Check Digit Verification of cas no
The CAS Registry Mumber 57830-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,3 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57830-48:
(7*5)+(6*7)+(5*8)+(4*3)+(3*0)+(2*4)+(1*8)=145
145 % 10 = 5
So 57830-48-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H5S2.BF4/c1-2-4-7-6(3-1)8-5-9-7;2-1(3,4)5/h1-5H;/q+1;-1
57830-48-5Relevant articles and documents
Ligandless Nickel-Catalyzed Ortho-Selective Directed Trifluoromethylthiolation of Aryl Chlorides and Bromides Using AgSCF3
Nguyen, Tin,Chiu, Weiling,Wang, Xinying,Sattler, Madeleine O.,Love, Jennifer A.
supporting information, p. 5492 - 5495 (2016/11/17)
A mild protocol for Ni-catalyzed trifluoromethylthiolation of aryl chlorides and bromides is described herein. The method utilizes AgSCF3 as an easily accessible nucleophilic trifluoromethylthiolating reagent and does not require any ligands or additives. Ortho-selectivity is achieved using a variety of directing groups such as imines, pyridines, and oxazolines for 24 examples in up to 95% yield.
