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7-chloro-5-(2-chlorophenyl)-3-hydroxy-1-(2-hydroxyethyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51230-35-4

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51230-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51230-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,3 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51230-35:
(7*5)+(6*1)+(5*2)+(4*3)+(3*0)+(2*3)+(1*5)=74
74 % 10 = 4
So 51230-35-4 is a valid CAS Registry Number.

51230-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-5-(2-chlorophenyl)-3-hydroxy-1-(2-hydroxyethyl)-3H-1,4-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names SAS 632

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:51230-35-4 SDS

51230-35-4Upstream product

51230-35-4Downstream Products

51230-35-4Relevant academic research and scientific papers

A new series of benzodiazepines. 1 hydroxyalkyl derivatives of 1,3 dihydro 2H 1,4 benzodiazepin 2 ones

Tamagnone,De Maria,De Marchi

, p. 720 - 722 (2007/10/09)

A series of new 1 hydroxyalkyl derivatives of 1,3 dihydro 2H 1,4 benzodiazepin 2 ones bearing a 3 hydroxyl or a 4 N oxide function together with some related compounds have been synthesized. Compound [1 (2 hydroxyethyl) 3 hydroxy 7 chloro 1,3 dihydro 5 (o fluorophenyl) 2H 1,4 benzodiazepin 2 one] has been selected for further studies both in animals and in humans as an antianxiety sedative agent.

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