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Acetaldehyde, (phenylimino)-, phenylhydrazone, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81429-29-0

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81429-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81429-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,2 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81429-29:
(7*8)+(6*1)+(5*4)+(4*2)+(3*9)+(2*2)+(1*9)=130
130 % 10 = 0
So 81429-29-0 is a valid CAS Registry Number.

81429-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (phenylimino)acetaldehyde phenylhydrazone

1.2 Other means of identification

Product number -
Other names 1,5-diphenyl-1,2,5-triazapentadiene

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:81429-29-0 SDS

81429-29-0Relevant academic research and scientific papers

The Thermolysis of Polyazapentadienes. Part 1. 1,5-Diaryl-1,2,5-triaza-derivatives

McNab, Hamish

, p. 2200 - 2204 (2007/10/02)

Flash vacuum pyrolysis of the title compounds at 600 deg C gives quinoxalines and arylamines, together with small quantities of nitriles, diarylamines, azobenzenes, and formamidines.The mechanism involves homolytic cleavage of the N-N bond to generate a conjugated iminyl radical, which can either cyclise to a quinoxaline, or fragment to simpler radicals which lead to the minor products by coupling reactions.

SYNTHESIS AND INVESTIGATION OF LIGANDS CONTAINING A HYDRAZONE GROUP V. SYNTHESIS OF IMINOHYDRAZONES OF UNSUBSTITUTED GLYOXAL

Shandurenko, G. V.,Avramenko, G. V.,Stepanov, B. I.

, p. 659 - 661 (2007/10/02)

The synthesis of glyoxal iminohydrazones was realised by the succesive reaction of glyoxal with arylhydrazines and aromatic amines.On the basis of spectral data they were assigned a chelate structure with an intramolecular hydrogen bond.

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