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21524-25-4

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21524-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21524-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21524-25:
(7*2)+(6*1)+(5*5)+(4*2)+(3*4)+(2*2)+(1*5)=74
74 % 10 = 4
So 21524-25-4 is a valid CAS Registry Number.

21524-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z)-4-chloro-6-(phenylhydrazinylidene)cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-Chloro-2-[(6-methoxy-3-pyridinyl)amino] benzoic acid

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:21524-25-4 SDS

21524-25-4Relevant articles and documents

Nanosilica/NaNO2: Novel heterogeneous system for synthesis of Azo compounds

Jirandehi, Hassan Fathinejad,Mirzaeian, Marjan,Mirzaeian, Mojtaba

experimental part, p. 376 - 377 (2011/07/07)

Various azo compounds are synthesized by electrophonic substitution reaction in the presence of Nanosilica/NaNO2as a catalyst. Copyright Taylor & Francis Group, LLC.

Synthesis of diaryl-azo derivatives as potential antifungal agents

Xu, Hui,Zeng, Xiwen

supporting information; experimental part, p. 4193 - 4195 (2010/08/22)

As compared with a commercially available agricultural fungicide hymexazol, some phenyl-azo phenol derivatives (e.g., 4a, 4b, 4f, 4n, 4q, 4u, and 4v) exhibited the more promising and pronounced antifungal activities in vitro against seven phytopathogenic fungi. It seemed that 4-((un)substituted phenylazo)-phenol and 4-((un)substituted phenylazo)-3-methylphenol might be considered as new lead structures for further design of agricultural fungicides.

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