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Benzaldehyde, (1-phenylethylidene)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55044-30-9

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55044-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55044-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,4 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55044-30:
(7*5)+(6*5)+(5*0)+(4*4)+(3*4)+(2*3)+(1*0)=99
99 % 10 = 9
So 55044-30-9 is a valid CAS Registry Number.

55044-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1E,2E)-1-benzylidene-2-(1-phenylethylidene)hydrazine

1.2 Other means of identification

Product number -
Other names Benzyliden-(1-phenyl-aethyliden)-hydrazin

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:55044-30-9 SDS

55044-30-9Relevant academic research and scientific papers

Rhodium(III)-catalyzed coupling of aromatic ketazines or oximes with 2-vinyloxirane via C-H activation

Wen, Jing,Wu, An,Miao, Yuqin,Zhu, Jin

supporting information, p. 5512 - 5516 (2015/09/21)

Described herein is a rhodium(III)-catalyzed coupling of aromatic ketazines or oximes with 2-vinyloxirane via directed C-H activation. This reaction proceeds efficiently under mild conditions with a low catalyst loading, especially in conditions with room temperature in the absence of additives for aromatic ketazines. A wide range of substituted substrates is supported and a possible mechanism is proposed according to the experimental results of kinetic isotopic effect, reversibility studies, and catalysis with rhodacycle intermediate c1.

A General Synthesis of Unsymmetrical Azines via N-(Diethoxyphosphinyl)-hydrazones

Koziara, Anna,Turski, Krzysztof,Zwierzak, Andrzej

, p. 298 - 301 (2007/10/02)

A new synthesis of unsymmetrical azines utilizing diethyl phosphorohydrazidate as starting material and based on Wadsworth-Emmons type phosphoramidate approach is discribed.

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