215732-90-4 Usage
General Description
3-(trifluoromethylthio)benzyl chloride is a chemical compound with the formula C8H6ClF3S. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. It is used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. 3-(TRIFLUOROMETHYLTHIO)BENZYL CHLORIDE 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.
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.
