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2-Benzothiazolebutyronitrile, also known as 2-(2-cyanoethyl)benzothiazole, is an organic compound with the chemical formula C11H8N2S. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The molecule features a butyronitrile group (a four-carbon chain with a nitrile group at the end) attached to the benzothiazole core. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure and properties, 2-Benzothiazolebutyronitrile plays a significant role in the development of new compounds with potential applications in various industries.

21344-52-5

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21344-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21344-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21344-52:
(7*2)+(6*1)+(5*3)+(4*4)+(3*4)+(2*5)+(1*2)=75
75 % 10 = 5
So 21344-52-5 is a valid CAS Registry Number.

21344-52-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,3-benzothiazol-2-yl)butanenitrile

1.2 Other means of identification

Product number -
Other names 2-benzothiazolebutyronitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21344-52-5 SDS

21344-52-5Downstream Products

21344-52-5Relevant academic research and scientific papers

Direct C-H Cyanoalkylation of Quinoxalin-2(1H)-ones via Radical C-C Bond Cleavage

Yang, Lin,Gao, Pin,Duan, Xin-Hua,Gu, Yu-Rui,Guo, Li-Na

, p. 1034 - 1037 (2018)

An efficient synthesis of cyanoalkylated heteroarenes via iron-catalyzed direct C-H cyanoalkylation of heteroarenes has been developed. Structurally diverse cyanoalkyl motifs generated through C-C bond cleavage of cyclobutanone oxime esters have been intr

Metal-Free Direct C-H Cyanoalkylation of Quinoxalin-2(1 H)-Ones by Organic Photoredox Catalysis

Zhang, Wei,Pan, Yu-Liang,Yang, Chen,Chen, Li,Li, Xin,Cheng, Jin-Pei

, p. 7786 - 7795 (2019)

Green and efficient C-C bond cleavage/cyanoalkylation of quinoxalin-2(1H)-ones and other heteroarenes under visible light or sunlight irradiation is described. The reaction proceeds under mild conditions at room temperature without transition-metal catalysts and extra bases. Notably, the products enable facile transformations to various significant organic compounds.

Minisci-Type C–H Cyanoalkylation of Heteroarenes Through N–O/C–C Bonds Cleavage

Jian, Yong,Chen, Ming,Yang, Chao,Xia, Wu-jiong

supporting information, p. 1439 - 1442 (2019/05/16)

A visible-light-induced C–H cyanoalkylation of heteroarenes was described, in which cycloketone oximes were readily transformed into carbon-centered radicals with a terminal cyano-group via N–O/C–C bonds cleavage in one phtochemical step. This reaction protocol displayed a broad substrate scope of heterocycle compounds, and it provided a promising strategy for the installation of cyanoalkyl groups onto heteroarenes.

Functionalized orthoesters as powerful building blocks for the efficient preparation of heteroaromatic bicycles

Bastug, Gulluzar,Eviolitte, Christophe,Markó, István E.

supporting information; experimental part, p. 3502 - 3505 (2012/08/08)

By combining substituted anilines with functionalized orthoesters, an efficient and connective methodology for the preparation of benzoxazole, benzothiazole, and benzimidazole derivatives has been established. The versatility of this approach enables the development of new libraries of heterocycles containing multifunctional sites.

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