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84031-17-4

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  • 1H-1,4-Benzodiazepine,7-bromo-5-(2-chlorophenyl)-2,3-dihydro-2-(methoxymethyl)-1-methyl-

    Cas No: 84031-17-4

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84031-17-4 Usage

Uses

Different sources of media describe the Uses of 84031-17-4 differently. You can refer to the following data:
1. Benzodiazepines. Used for antidepressant.
2. A QTrap liquid chromatography/ tandem mass spectrometry system is used in analysis to identify 7-Bromo-5-(2-chlorophenyl)-2,3-dihydro-2-(methoxymethyl)-1-methyl-1H-1,4-benzodiazepine

Check Digit Verification of cas no

The CAS Registry Mumber 84031-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,3 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84031-17:
(7*8)+(6*4)+(5*0)+(4*3)+(3*1)+(2*1)+(1*7)=104
104 % 10 = 4
So 84031-17-4 is a valid CAS Registry Number.

84031-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromo-1-methyl-2-methoxymethyl-5-(2'-chlorophenyl)-2,3-dihydro-1H-1,4-benzodiazepin

1.2 Other means of identification

Product number -
Other names metaclazepam

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:84031-17-4 SDS

84031-17-4Relevant articles and documents

1,4-Benzodiazepine and 1,5-benzodiazocines. VII. Synthesis and biological activity

Milkowski,Liepman,Zeugner,et al.

, p. 345 - 358 (2007/10/02)

Synthesis of a new class of 2,3,-dihydro-1H-1,4-benzodiazepines and of the corresponding 1,2,3,4-tetrahydro-1,5-benzodiazocines is described. The biological activity of the compounds is evaluated in vivo by measuring their inhibition of pentetrazole induced seizures and in vitro by determining their affinity for the benzodiazepine receptor. Comparison of both tests reveals differences between activity in vivo and in vitro which are discussed.

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