672324-84-4 Usage
Description
4-(1,3-thiazol-2-yl)benzonitrile, with the molecular formula C10H6N2S, is a chemical compound belonging to the thiazole class of organic compounds. It features a five-membered sulfur-heterocycle fused to a benzene ring, making it a versatile building block in organic synthesis.
Uses
Used in Pharmaceutical Synthesis:
4-(1,3-THIAZOL-2-YL)BENZONITRILE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-(1,3-THIAZOL-2-YL)BENZONITRILE serves as a crucial component in the creation of pesticides and other agrochemicals. Its incorporation can lead to the development of more effective and targeted products for agricultural use.
Used in Organic Electronic Devices:
4-(1,3-THIAZOL-2-YL)BENZONITRILE is also being investigated for its potential use in organic electronic devices. Its electronic properties make it a promising candidate for applications such as organic light-emitting diodes (OLEDs) and organic solar cells, where it can contribute to improved performance and efficiency.
Overall, 4-(1,3-THIAZOL-2-YL)BENZONITRILE is a valuable compound with diverse applications across multiple industries, including pharmaceuticals, agrochemicals, and organic electronics. Its versatility and potential for further research and development make it an important player in the field of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 672324-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,3,2 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 672324-84:
(8*6)+(7*7)+(6*2)+(5*3)+(4*2)+(3*4)+(2*8)+(1*4)=164
164 % 10 = 4
So 672324-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H6N2S/c11-7-8-1-3-9(4-2-8)10-12-5-6-13-10/h1-6H
672324-84-4Relevant articles and documents
DDQ-induced dehydrogenation of heterocycles for c-c double bond formation: Synthesis of 2-thiazoles and 2-oxazoles
Li, Xiangnan,Li, Cheng,Yin, Bing,Li, Cong,Liu, Ping,Li, Jianli,Shi, Zhen
, p. 1408 - 1411 (2013/07/26)
Strong as an Ox: 2-Thiazoles and 2-oxazoles are formed by oxidation of 2-thiazolines and 2-oxazolines without requiring substituents at the C4 and C5 positions. DDQ plays an important role as the oxidant in this transformation and metal is unnecessary. This general procedure shows good functional group tolerance and provides a wide variety of 2-thiazoles and 2-oxazoles in moderate to excellent yields.
Cobalt-catalyzed C-SMe bond activation of heteroaromatic thioethers
Begouin, Jeanne-Marie,Rivard, Michael,Gosmini, Corinne
supporting information; experimental part, p. 5972 - 5974 (2010/11/02)
Cobalt-catalyzed activation of methylthio-substituted N-heterocycles facilitates either cross-coupling reactions with aryl- or benzylzinc compounds or synthesis of the corresponding zinc compounds.
Pd-PEPPSI-IPent: Low-temperature negishi cross-coupling for the preparation of highly functionalized, tetra-ortho-substituted biaryls
Calimsiz, Selcuk,Sayah, Mahmoud,Mallik, Debasis,Organ, Michael G.
supporting information; experimental part, p. 2014 - 2017 (2010/06/20)
(Chemical Equation Presented) Cool couplings: Complex, hindered biaryls have been prepared at temperatures ranging from 0°C to room temperature, or with gentle heating. The Pd-PEPPSI-IPent catalyst (see scheme) nicely couples starting materials containing acidic moieties and routinely prepares biaryl derivatives where one or both rings comprising the biaryl are heterocyclic. Ar1=hindered aryl or heteroaryl, Ar2=unactivated aryl or heteroaryl.
