16296-79-0 Usage
Uses
Used in Pharmaceutical Industry:
5-CHLORO-1-BENZOTHIOPHENE-3-CARBONITRILE is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and reactivity, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-CHLORO-1-BENZOTHIOPHENE-3-CARBONITRILE serves as a key intermediate in the production of agrochemicals, aiding in the development of effective pesticides and other agricultural chemicals.
Used in Organic Synthesis:
5-CHLORO-1-BENZOTHIOPHENE-3-CARBONITRILE is utilized as a precursor in organic synthesis, enabling the creation of a wide range of chemical compounds for various applications.
Used in Dye and Pigment Production:
5-CHLORO-1-BENZOTHIOPHENE-3-CARBONITRILE is employed as a starting material for the production of dyes and pigments, thanks to its chemical properties that facilitate color development and stability.
Used in Material Science:
5-CHLORO-1-BENZOTHIOPHENE-3-CARBONITRILE has shown potential in material science, particularly in the development of new materials with unique properties for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 16296-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,9 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16296-79:
(7*1)+(6*6)+(5*2)+(4*9)+(3*6)+(2*7)+(1*9)=130
130 % 10 = 0
So 16296-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H4ClNS/c10-7-1-2-9-8(3-7)6(4-11)5-12-9/h1-3,5H
16296-79-0Relevant academic research and scientific papers
Guo, Songjin,Wan, Gen,Sun, Song,Jiang, Yan,Yu, Jin-Tao,Cheng, Jiang
, p. 5085 - 5088 (2015)
The development of organic transformation using cheap and readily available substrates under mild conditions will be pivotal for green and sustainable synthetic organic chemistry. Concerning our continued interest in the cyanation reaction, a metal-free direct ammoxidation of readily available methyl arenes leading to nitriles was established under mild conditions. A series of aryl methanes especially heteroaryl methanes (30 examples) were applicable in moderate to good yields with good functionality tolerance.