215732-90-4 Usage
Description
3-(TRIFLUOROMETHYLTHIO)BENZYL CHLORIDE, with the chemical formula C8H6ClF3S, is a white crystalline solid that is insoluble in water but soluble in organic solvents. It is a versatile building block in organic chemistry due to the presence of both a benzyl group and a trifluoromethylthio group, which can participate in a variety of chemical reactions to form new carbon-carbon or carbon-heteroatom bonds. The trifluoromethylthio group also imparts unique chemical and physical properties to the molecule, making it of interest in the development of new materials and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
3-(TRIFLUOROMETHYLTHIO)BENZYL CHLORIDE is used as a reagent in organic synthesis for the preparation of pharmaceuticals. Its unique chemical and physical properties, as well as its ability to form new bonds, make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
3-(TRIFLUOROMETHYLTHIO)BENZYL CHLORIDE is also used as a reagent in organic synthesis for the preparation of agrochemicals. Its versatility in forming new bonds and imparting unique properties to molecules makes it a useful building block in the development of new agrochemical products.
Used in Material Science:
3-(TRIFLUOROMETHYLTHIO)BENZYL CHLORIDE is used as a building block in the development of new materials. Its unique properties and ability to form new bonds make it a promising candidate for creating innovative materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 215732-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,7,3 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 215732-90:
(8*2)+(7*1)+(6*5)+(5*7)+(4*3)+(3*2)+(2*9)+(1*0)=124
124 % 10 = 4
So 215732-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClF3S/c9-5-6-2-1-3-7(4-6)13-8(10,11)12/h1-4H,5H2
215732-90-4Relevant articles and documents
Imidodisulfamides. I. A novel class of antagonists of slow-reacting substance of anaphylaxis
El-Fehail Ali,Dandridge,Gleason,et al.
, p. 947 - 952 (2007/10/02)
A series of N',N''-bis(aryl)- and N',N''-(aralkyl)imidodisulfamides was prepared and evaluated as antagonists of slow-reacting substance of anaphylaxis (SRS-A) induced contractions of isolated guinea pig ileum. Some of these compounds, notably N',N''-bis(4-phenylbutyl)- N',N''-bis[2-(4-chlorophenyl)ethyl]-, and N',N''-bis[2-(4-bromophenyl)ethyl]imidodisulfamides (16, 22, and 26), were moderately potent and selective antagonists of SRS-A. The influence of lipophilic (π) and electronic (σ) factors on SRS-A antagonist activity appears to be of considerable importance to the derivation of potent and selective SRS-A antagonists.