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2562-74-5

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2562-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2562-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2562-74:
(6*2)+(5*5)+(4*6)+(3*2)+(2*7)+(1*4)=85
85 % 10 = 5
So 2562-74-5 is a valid CAS Registry Number.

2562-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1H-benzo-imidazol-2-yl)-N,N-diethylaniline

1.2 Other means of identification

Product number -
Other names 2-acetyl-5-benzylthiophene

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:2562-74-5 SDS

2562-74-5Relevant articles and documents

Pharmacological and Toxicological Screening of Novel Benzimidazole-Morpholine Derivatives as Dual-Acting Inhibitors

Can, Nafiz nc,Evik, Ulviye Acar,Sagl?k, Beg m Nurpelin,Zkay, Yusuf,Atl?, Zlem,Baysal, Merve,Zkay, mide Demir,Can, zg r Devrim

, (2017/08/30)

The aim of this study was to investigate acetylcholinesterase (AChE), monoamine oxidase A (MAO-A), monoamine oxidase B (MAO-B), cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) enzyme inhibitory, and antimicrobial activities of a new series of 2-(4-s

One-pot synthesis of benzimidazoles and benzothiazoles in the presence of Fe(HSO4)3 as a new and efficient oxidant

Eshghi, Hossein,Rahimizadeh, Mohammad,Shiri, Ali,Sedaghat, Parisa

experimental part, p. 515 - 518 (2012/04/23)

A series of substituted benzimidazoles and benzothiazoles were prepared through the one-pot reaction of ophenylenediamine and o-aminothiophenol with various aldehydes in the presence of ferric hydrogensulfate both in EtOH and water as solvent. The reactions proceed smoothly in excellent yield, high chemoselectivity and with an easy work-up.

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