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Propanediamide, 2-bromo-N,N'-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

333309-96-9

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333309-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333309-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,0 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 333309-96:
(8*3)+(7*3)+(6*3)+(5*3)+(4*0)+(3*9)+(2*9)+(1*6)=129
129 % 10 = 9
So 333309-96-9 is a valid CAS Registry Number.

333309-96-9SDS

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 N,N'-dibenzyl-2-bromopropanediamide

1.2 Other means of identification

Product number -
Other names N,N'-dibenzyl-2-bromo-malonamide

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:333309-96-9 SDS

333309-96-9Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS, MEDICAMENTS CONTAINING SAID COMPOUNDS, USE THEREOF AND PROCESSES FOR THE PREPARATION THEREOF

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Paragraph 0197-0199, (2014/04/03)

The present invention relates to compounds of general formula (I) and the tautomers and the salts thereof, particularly the pharmaceutically acceptable salts thereof, which have valuable pharmacological properties, particularly an inhibitory effect on epithelial sodium channels, the use thereof for the treatment of diseases, particularly diseases of the lungs and airways.

Bromination of N,N′-substituted malonodiamides

Georiyants,Bezuglyi

, p. 1079 - 1081 (2007/10/03)

Aiming at preparation of biologically active compounds a bromination of N,N′-substituted malonodiamides in a glacial acetic acid was carried out. The use of one equiv of bromine provided monobromo derivatives, with two equiv of bromine dibromo-substituted

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