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Benzaldehyde, 3,4-dichloro-, [1-(4-chlorophenyl)-4(1H)-pyridinylidene]hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62906-53-0

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62906-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62906-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62906-53:
(7*6)+(6*2)+(5*9)+(4*0)+(3*6)+(2*5)+(1*3)=130
130 % 10 = 0
So 62906-53-0 is a valid CAS Registry Number.

62906-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-(4-Chloro-phenyl)-1H-pyridin-4-ylidene]-N'-[1-(3,4-dichloro-phenyl)-meth-(E)-ylidene]-hydrazine

1.2 Other means of identification

Product number -
Other names -

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:62906-53-0 SDS

62906-53-0Upstream product

62906-53-0Downstream Products

62906-53-0Relevant academic research and scientific papers

1-Substitutedphenyl-4(1H)-pyridinone hydrazones

-

, (2008/06/13)

Novel 1-Substitutedphenyl-4(1H)-pyridinone hydrazones are prepared by reacting 1-substitutedpheny-4(1H)-pyridinone hydrazone with substituted benzaldehydes. The novel hydrazones are useful as anticoccidial agents.

Anticoccidial 1 substituted 4(1H) pyridinone hydrazones

Douglas,Fisher,Fishinger,Gund,Harris,Olson,Patchett,Ruyle

, p. 939 - 943 (2007/10/04)

4 Chlorobenzaldehyde 1 (4 chlorophenyl) 4(1h) pyridinylidene hydrazone fluorosulfonate (4) was found to have excellent anticoccidial activity in chickens. The synthesis and biological evaluation of related analogues are presented. Presumably 4 shares a common mechanism of action with Robenidine (25) since it was not active on a robenidine tolerant strain of E. tenella. Structural comparisons of the two molecules are presented.

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