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1H-Benzimidazole-1-butanenitrile(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58553-97-2

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58553-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58553-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58553-97:
(7*5)+(6*8)+(5*5)+(4*5)+(3*3)+(2*9)+(1*7)=162
162 % 10 = 2
So 58553-97-2 is a valid CAS Registry Number.

58553-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzimidazol-1-yl)butanenitrile

1.2 Other means of identification

Product number -
Other names 1h-benzimidazole-1-butanenitrile

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:58553-97-2 SDS

58553-97-2Downstream Products

58553-97-2Relevant academic research and scientific papers

Copper-Catalyzed Cyanoalkylation of Amines via C-C Bond Cleavage: An Approach for C(sp3)-N Bond Formations

Yang, Lin,Zhang, Jia-Yu,Duan, Xin-Hua,Gao, Pin,Jiao, Jiao,Guo, Li-Na

, p. 8615 - 8629 (2019/08/30)

The efficient copper-catalyzed cyanoalkylation of amines via C-C bond cleavage has been demonstrated. Distinctive features of this procedure involves mild conditions, broad range of nitrogen nucleophiles, high selectivity, and good functional group tolerance, thus providing a useful approach for the C(sp3)-N bond formations. Most importantly, this protocol is applicable to the late-stage functionalization of natural products, amino acid esters, and drugs. Mechanistic studies suggest that a radical intermediate was involved in this transformation.

Benzimidazole-based silver(I)-N-heterocyclic carbene complexes as anti-bacterials: Synthesis, crystal structures and nucleic acids interaction studies

Asekunowo, Patrick O.,Haque, Rosenani A.,Razali, Mohd. R.,Budagumpi, Srinivasa

, p. 126 - 137 (2015/03/30)

A series of new benzimidazolium salts as N-heterocyclic carbene (NHC) precursors has been synthesized. Reactions of these salts with Ag2O with varying metal-to-salt ratio facilitate the formation of a series of new binuclear and mononuclear Ag(I)-NHC complexes. All compounds were characterized using physicochemical and spectroscopic techniques. Single-crystal X-ray diffraction study reveals a binuclear structure for one of the complexes and a mononuclear one for two others. These complexes exist as cationic Ag(I)-NHC complexes with the chelation of carbene carbons to the silver centre in an almost linear manner. The compounds were screened for their anti-bacterial activities against Staphylococcus aureus (ATCC 12600) as a Gram-positive bacterium and Escherichia coli (ATCC 25922) as a Gram-negative bacterium. The results show that both bacteria appear markedly inhibited. Furthermore, the results suggest the possibility of steric variation as a modulation of the anti-bacterial activities. The nuclease activities of the compounds were assessed using gel electrophoresis and the results indicate that these complexes can cleave or degrade DNA and RNA via a non-oxidative mechanism.

Hofmann-type elimination in the efficient N-alkylation of azoles: Imidazole and benzimidazole

Horvath

, p. 102 - 106 (2007/10/02)

A simple and efficient preparation of 1-substituted 1H-azoles (imidazole and benzimidazole) has been developed, which involves a selective Hofmann-type elimination of the 2-cyanoethyl group from the azolium salts obtained by the reaction of halides with 1H-imidazole-1-propanenitrile and 1H-benzimidazole-1-propanenitrile. Overall yields of 1-substituted 1H-azoles decreased in the order: primary alkyl halides ≥ allylhalides ≥ secondary alkyl halides ≥ benzyl halides > α-keto halides, in relation to the alkylating agent, and imidazole ≥ benzimidazole, in relation to the azole, respectively.

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