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Diazene, (1-methylethenyl)phenyl-, (1E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41350-48-5

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41350-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41350-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,5 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41350-48:
(7*4)+(6*1)+(5*3)+(4*5)+(3*0)+(2*4)+(1*8)=85
85 % 10 = 5
So 41350-48-5 is a valid CAS Registry Number.

41350-48-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl(prop-1-en-2-yl)diazene

1.2 Other means of identification

Product number -
Other names 2-Phenylazo-1-propen

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:41350-48-5 SDS

41350-48-5Relevant academic research and scientific papers

New heterocyclic precursors for thermal generation of reactive, electron-rich 1,2-diaza-1,3-butadienes

Boeckman Jr., Robert K.,Ge, Ping,Reed, Jessica E.

, p. 3647 - 3650 (2007/10/03)

Figure presented The preparation and thermolysis of new stable heterocyclic precursors of 1,2-diaza-1,3-butadienes is described. The resulting reactive diazadienes are trapped in situ with N-phenyldiazamaleimide. The effect of precursor structure on the temperature at which the diazadienes are generated is discussed.

N-ARENESULFONYL-N-PHENYLHYDRAZONES

Schantl, J.G.,Hebeisen, P.,Karpellus, P.

, p. 39 - 48 (2007/10/02)

The phenylhydrazones of aliphatic aldehydes and ketones, and those of benzaldehyde and benzophenone react with various sulfonylchlorides in the presence of a suitable base to give the title compounds; examples of their synthetic use are given.

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