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50-97-5

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50-97-5 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 54, p. 2949, 1989 DOI: 10.1021/jo00273a032

Check Digit Verification of cas no

The CAS Registry Mumber 50-97-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50-97:
(4*5)+(3*0)+(2*9)+(1*7)=45
45 % 10 = 5
So 50-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O/c17-13(10-6-2-1-3-7-10)14-15-11-8-4-5-9-12(11)16-14/h1-9,13,17H,(H,15,16)

50-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-benzimidazol-2-yl(phenyl)methanol

1.2 Other means of identification

Product number -
Other names EINECS 200-073-0

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:50-97-5 SDS

50-97-5Relevant articles and documents

NOVEL ONE-POT HOMOGENEOUS PROCESS FOR THE LARGE SCALE MANUFACTURE OF 2-SUBSTITUTED BENZIMIDAZOLES

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Paragraph 0147; 0148, (2019/05/24)

2-substituted benzimidazoles and methods of preparing the same are disclosed. The compositions may include a compound or salt thereof, an acid, and a polar aprotic solvent. The compositions may be used to inhibit corrosion of a metal surface in contact with an aqueous system, and provide enhanced protection against corrosion of metals in the aqueous system.

BENZAZOLE DERIVATIVES AS HISTAMINE H4 RECEPTOR LIGANDS

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Page/Page column 63, (2012/04/17)

The present patent application concerns new Iigands of the H4-receptor of formula (I), their process of preparation and their therapeutic use.

The synthesis, characterization and optical properties of novel pyrido[1,2-a]benzimidazole derivatives

Ge, Yan Qing,Jia, Jiong,Yang, He,Tao, Xu Tang,Wang, Jian Wu

scheme or table, p. 344 - 349 (2011/06/11)

A series of novel, substituted, pyrido[1,2-a]benzimidazole derivatives were synthesized using a novel tandem annulation reaction between 2-acylbenzimidazole derivatives and 4-bromobut-2-enoic esters under mild conditions. The compounds were characterized using IR, 1H NMR, 13C NMR and HRMS; the crystal structure of 2,7,8-trimethyl-3- ethoxycarbonyl-4-phenylpyrido[1,2-a]benzimidazole was determined as orthorhombic. The absorbance and fluorescence spectra of the pyrido[1,2-a]benzimidazoles were measured in dichloromethane; an intense absorption maxima was observed at 250 nm and emission maxima were noted at 460 nm. The absorption spectra and fluorescence characteristics of the pyrido[1,2-a]benzimidazole derivatives revealed that a phenyl and a methyl group attached to the pyrido[1,2-a]benzimidazole ring markedly influenced maximum emission.

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