82174-09-2 Usage
Uses
Used in Organic Synthesis:
3-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is used as a reagent in organic synthesis for its strong nucleophilic properties, enabling the preparation of a wide range of pharmaceutical and agrochemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is utilized as a key intermediate in the development of new drugs, thanks to its unique chemical structure and reactivity.
Used in Agrochemicals:
3-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is employed as a starting material in the synthesis of various agrochemicals, contributing to the development of effective pest control solutions.
Used in Antimicrobial Applications:
3-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE has been shown to exhibit fungicidal and bactericidal properties, making it a potential candidate for use in antimicrobial formulations across different industries, including healthcare and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 82174-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,7 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82174-09:
(7*8)+(6*2)+(5*1)+(4*7)+(3*4)+(2*0)+(1*9)=122
122 % 10 = 2
So 82174-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F3NS/c10-9(11,12)14-8-3-1-2-7(6-8)4-5-13/h1-3,6H,4H2
82174-09-2Relevant 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.
