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2H-1,5-Benzodiazepin-2-one, 1,3-dihydro-4-methyl-8-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37546-88-6

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37546-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37546-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,4 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37546-88:
(7*3)+(6*7)+(5*5)+(4*4)+(3*6)+(2*8)+(1*8)=146
146 % 10 = 6
So 37546-88-6 is a valid CAS Registry Number.

37546-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-8-nitro-2,3-dihydro-1,5-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names 4-methyl-8-nitro-1,3-dihydro-benzo[b][1,4]diazepin-2-one

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:37546-88-6 SDS

37546-88-6Relevant academic research and scientific papers

Synthese de Nouvelles 4-Acetonylidene-1,5-benzodiazepin-2-ones III: Etude de la Reaction de Condensation des o-Phenylenediamines monosubstituees avec la γ-pyrone

Abbassi, M. El,Essassi, E. M.,Fifani, J.

, p. 205 - 210 (2007/10/03)

Condensation of unsymmetrical aromatic diamines (4-methyl-, 4-chloro-, and 4-nitrophenylenediamines) 2-4 with 2-hydroxy-6-methyl-4-pyrone 1 have been examinated. The structure of isomerie 4-acetonylidene-1,5-benzodiazepin-2-ones 5-10 and benzimidazoles 11-16 obtained from competitive reactions have been established by the spectrale data (1H NMR, IR and mass spectrum). The position of the substituents in 6/9 and 7/10 was proved by comparison with samples with authentic structures.

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