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

112055-25-1

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112055-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112055-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,5 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112055-25:
(8*1)+(7*1)+(6*2)+(5*0)+(4*5)+(3*5)+(2*2)+(1*5)=71
71 % 10 = 1
So 112055-25-1 is a valid CAS Registry Number.

112055-25-1SDS

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 2,4-bis(4-methylphenyl)-3H-1,5-benzodiazepine

1.2 Other means of identification

Product number -
Other names 2,4-di(p-tolyl)-3H-1,5-benzodiazepine

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:112055-25-1 SDS

112055-25-1Relevant academic research and scientific papers

Asymmetric hydrogenation of 2,4-disubstituted 1,5-benzodiazepines using cationic ruthenium diamine catalysts: An unusual achiral counteranion induced reversal of enantioselectivity

Ding, Zi-Yuan,Chen, Fei,Qin, Jie,He, Yan-Mei,Fan, Qing-Hua

supporting information; experimental part, p. 5706 - 5710 (2012/07/14)

BArFing it out the other way: A highly enantioselective hydrogenation of 2,4-disubstituted 1,5-benzodiazepines using chiral cationic ruthenium diamine catalysts (R,R)-1 has been developed (see scheme; BArF=tetrakis(3,5- bistrifluoromethylphenyl)borate). E

Addition of Dihalocarbenes to 3H-1,5-Benzodiazepines. Synthesis of 2H-Bisazirinobenzodiazepines

Takahashi, Masahiko,Takada, Tsugumasa,Sakagami, Takeshi

, p. 797 - 799 (2007/10/02)

Addition of dihalocarbenes, generated from haloforms using a phase transfer catalyst, to 3H-1,5-benzodiazepines gave 2H-Bisazirinobenzodiazepines, a new ring system.

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