7357-70-2 Usage
Description
2-Cyanothioacetamide is an organic compound that serves as a key building block in the synthesis of various chemical compounds, particularly in the production of 2-pyridothiones. It is characterized by its unique molecular structure, which features a cyano group, a thioacetamide group, and a carbonitrile group. This versatile compound is known for its potential applications in various industries, including agrochemical, pharmaceutical, and dyestuff fields.
Uses
Used in Chemical Synthesis:
2-Cyanothioacetamide is used as a building block for the synthesis of 2-pyridothiones, which are a class of heterocyclic compounds with diverse applications in various fields. Its unique molecular structure allows it to be a valuable component in the creation of these compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Cyanothioacetamide is used as a precursor in the development of new and effective pesticides and other agricultural chemicals. Its role in the synthesis of 2-pyridothiones makes it a valuable resource for creating innovative products that can help improve crop protection and yield.
2-Cyanothioacetamide is used as a chemical intermediate for the development of new agrochemical products, contributing to the advancement of the industry and the creation of more effective solutions for agricultural challenges.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Cyanothioacetamide is utilized as a key component in the synthesis of various drug candidates. Its involvement in the production of 2-pyridothiones makes it a crucial element in the development of new medications with potential therapeutic benefits.
2-Cyanothioacetamide is used as a building block for the synthesis of pharmaceutical compounds, playing a significant role in the discovery and creation of novel drugs with the potential to treat various diseases and medical conditions.
Used in Dyestuff Industry:
In the dyestuff industry, 2-Cyanothioacetamide is employed as a starting material for the production of various dyes and pigments. Its unique chemical properties make it suitable for use in the creation of a wide range of colorants used in different applications, such as textiles, plastics, and printing inks.
2-Cyanothioacetamide is used as a raw material for the synthesis of dyes and pigments, contributing to the development of new and innovative colorants for various industries and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7357-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7357-70:
(6*7)+(5*3)+(4*5)+(3*7)+(2*7)+(1*0)=112
112 % 10 = 2
So 7357-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H4N2S/c4-2-1-3(5)6/h1H2,(H2,5,6)
7357-70-2Relevant articles and documents
Synthesis and Properties of New Fluorine-Containing Thieno[2,3-b]pyridine Derivatives
Buryi,Dotsenko,Aksenov,Aksenova
, p. 1744 - 1751 (2019)
Cyanothioacetamide reacted with 1,1,5,5-tetrafluoroacetylacetone to give 4,6-bis(difluoromethyl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile, and alkylation of the latter with α-chloroacetamides afforded 3-amino-4,6-bis(difluoromethyl)thieno[2,3-b]pyridine-2-carboxamides. The structure of the key compounds was proved using two-dimensional NMR techniques. In silico analysis of potential biological activity and bioavailability of the synthesized compounds was performed.
New Multicomponent Synthesis of Functionalized Nitriles and Esters of 6-Alkylsulfanyl-1,4-dihydronicotinic Acids
Dyachenko, V. D.,Kalashnik, I. N.
, p. 357 - 366 (2020/04/27)
Abstract: The multicomponent condensation of malononitrile, hydrogen sulfide, aryl orhetaryl aldehydes, 1,3-dicarbonyl compounds and alkylating reagents affordedfunctionalized nitriles and esters of 6-alkylsulfanyl-1,4-dihydronicotinicacids, their aromatic analogues and 1,4-dihydrothieno[2,3-b]pyridines.
Synthesis and Properties of 4,6-Dimethyl-5-pentyl-2-thioxo-1,2-dihydropyridine-3-carbonitrile and 3-Amino-4,6-dimethyl-5-pentylthieno[2,3-b]pyridines
Buryi,Dotsenko,Aksenov,Aksenova,Krivokolysko,Dyadyuchenko
, p. 1575 - 1585 (2019/10/14)
The reaction of 3-pentylpentane-2,4-dione with cyanothioacetamide afforded 4,6-dimethyl-5-pentyl-2-thioxo-1,2-dihydropyridine-3-carbonitrile. Alkylation of the latter led to the formation of 2-alkylsulfanyl-4,6-dimethyl-5-pentylpyridine-3-carbonitriles or 3-amino-4,6-dimethyl-5-pentylthieno[2,3-b]pyridines, depending on the alkylating agent and reaction conditions. The structures of the key compounds were proved by 2D NMR spectroscopy and X-ray analysis. Biological activity of the synthesized compounds was evaluated in silico. Some compounds were experimentally found to stimulate growth of sunflower seedlings.
