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DiazepaM IMpurity F is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31269-33-7

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31269-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31269-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,6 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31269-33:
(7*3)+(6*1)+(5*2)+(4*6)+(3*9)+(2*3)+(1*3)=97
97 % 10 = 7
So 31269-33-7 is a valid CAS Registry Number.

31269-33-7SDS

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-2-methoxy-5-phenyl-3H-1,4-benzodiazepine

1.2 Other means of identification

Product number -
Other names Diazepam Impurity F (BP)

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:31269-33-7 SDS

31269-33-7Downstream Products

31269-33-7Relevant articles and documents

Phosphorylation of cyclic amides

-

, (2008/06/13)

Compounds of the general formula STR1 are reacted with a strong base followed by a phosphorylating agent, such as dicyclicaminophosphinic halide or bis-di-lower alkylaminophosphinic halide to produce an imine of the formula STR2 wherein R is dicyclicaminophosphinyloxy or bis-di-lower alkylaminophosphinyloxy. R represents a leaving group which will undergo nucleophilic displacement with nitrogen, oxygen, sulfur and carbon containing nucleophiles, that is, nucleophiles which have, as a reactive site, a nitrogen, oxygen, sulfur or carbon atom, such that, when the cyclic imine undergoes nucleophilic displacement, there is formed C--N, C--O, C--S and C--C bonds between the carbon atom of the cyclic imine and the nucleophilic group. The end products may be utilized as intermediates in the production of pharmaceutically valuable compounds and, in some instances, are pharmaceutically valuable compounds per se.

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