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Benzamide, N-[1-(1H-benzimidazol-2-yl)-2-phenylethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30384-83-9

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30384-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30384-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,8 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30384-83:
(7*3)+(6*0)+(5*3)+(4*8)+(3*4)+(2*8)+(1*3)=99
99 % 10 = 9
So 30384-83-9 is a valid CAS Registry Number.

30384-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-(1H-benzimidazol-2-yl)-2-phenylethenyl]benzamide

1.2 Other means of identification

Product number -
Other names -

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:30384-83-9 SDS

30384-83-9Downstream Products

30384-83-9Relevant academic research and scientific papers

Synthesis and antimicrobial screening of N-[2-(2/4-substituted phenyl)-1-(5/6 substituted 1H- benzimidazol-2-yl)vinyl]benzamides

Kaushik, Darpan,Khan, Suroor A.,Chawla, Gita,Panda, Bibhu P.

experimental part, p. 629 - 636 (2012/08/29)

A series of (benzamidostyryl)benzimidazole derivatives were synthesized by hydrolyzing 2-phenyl-4-(substituted)benzylidene-5-oxazolones, the azlactone precursors in an acidic medium and treating the product with substituted o-phenylenediamine (OPDA) in si

Microwave-assisted solvent-dependent reaction: Chemoselective synthesis of quinoxalin-2(1 H)-ones, benzo[ d]imidazoles and dipeptides

Wang, Shu-Liang,Ding, Jie,Jiang, Bo,Gao, Yuan,Tu, Shu-Jiang

supporting information, p. 572 - 577 (2011/11/06)

A microwave-assisted solvent-dependent chemoselective reaction dealing with 4-arylidene-2-phenyloxazol-5-ones and diverse ortho-diamines to achieve three types of molecular scaffolds, 3-benzylquinoxalin-2(1H)-ones, benzimidazole and β-amino dipeptides is

Reaction of o-Phenylenediamine with 2-Oxazolin-5-ones

Tikdari, Ahmad M.,Mukerjee, Arya K.

, p. 73 - 74 (2007/10/02)

The reaction of o-phenylenediamine (2) with 2-oxazolin-5-ones (1a-c) gives benzimidazoles (4a-c) in the presence of gl. acetic acid.The intermediates 3a,b can be isolated only under neutral conditions. 4-(o-Aminoanilinomethylene)-2-phenyl-2-oxazolin-5-one (5) is formed, on heating 1d with 2, which is resistant to ring expansion.

BEHAVIOUR OF O-PHENYLENEDIAMINE AND O-AMINOTHIOPHENOL WITH AZIACTONES. A NEW SYNTHESIS OF SOME BENZIMIDAZOLE AND BENZOTHIAZOLE DERIVATIVES

Harb, Abdel-Fattah A.,Zayed, Salem E.,El-Maghraby, Awatef M.,Metwally, Saoud A.

, p. 1873 - 1881 (2007/10/02)

A new route for the preparation of benzimidazoles (5) and benzothiazoles (10) is described. o-Phenylenediamine reacted with 2-aryl-4-arylidene-2-oxazolin-5-ones to give the corresponding benzimidazole derivatives (5) while o-aminothiophenol produced eithe

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