215732-90-4 Usage
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 academic research and scientific papers
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.
