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105273-83-4

1H-1,5-Benzodiazepine, 8-chloro-2,3-dihydro-2-methyl-2,4-bis(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105273-83-4

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105273-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105273-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105273-83:
(8*1)+(7*0)+(6*5)+(5*2)+(4*7)+(3*3)+(2*8)+(1*3)=104
104 % 10 = 4
So 105273-83-4 is a valid CAS Registry Number.

105273-83-4SDS

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 8-Chloro-2-methyl-2,4-bis-(4-nitro-phenyl)-2,3-dihydro-1H-benzo[b][1,4]diazepine

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:105273-83-4 SDS

105273-83-4Downstream Products

105273-83-4Relevant articles and documents

Assessment of elementary derivatives of 1,5-benzodiazepine as anticancer agents with synergy potential

Gawandi, Sinthiya J.,Joshi, Shrinivas,Pissurlenkar, Raghuvir R.,Shingade, Sunil,desai, Vidya G.

, (2021/12/10)

Herein, we designed and synthesized 1,5-benzodiazepines as a lead molecule for anticancer activity and as potent synergistic activity with drug Methotrexate. Working under the framework of green chemistry principles, series of 1,5-benzodiazepine derivativ

DERIVATIVES OF 2,3-DIHYDRO-1H-1,5-BENZODIAZEPINE BASED ON SUBSTITUTED 1,2-PHENYLENEDIAMINES AND ACETYLARENES

Orlov, V. D.,Desenko, S. M.

, p. 1377 - 1381 (2007/10/02)

Derivatives of 2,3-dihydro-1H-1,5-benzodiazepine were obtained by the reaction of 4-chloro-, 4-bromo- 3,5-dichloro, and 4-cyano-substituted ortho-phenyl-enediamines with 4-R-acetophenones in the presence of concentrated sulfuric acid.Electronwithdrawing g

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