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2,6-dichloro-4-phenylazo-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146901-66-8

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146901-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146901-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,0 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 146901-66:
(8*1)+(7*4)+(6*6)+(5*9)+(4*0)+(3*1)+(2*6)+(1*6)=138
138 % 10 = 8
So 146901-66-8 is a valid CAS Registry Number.

146901-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-phenylazo-phenol

1.2 Other means of identification

Product number -
Other names 3.5-Dichlor-4-oxy-azobenzol

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:146901-66-8 SDS

146901-66-8Relevant academic research and scientific papers

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 some aryl azo-compounds under mild conditions

Jirandehi, Hasan Fathinejad,Mobinikhaledi, Akbar

experimental part, p. 6851 - 6854 (2012/07/03)

Some aryl azo compounds 2(a-h) were synthesized by reaction of corresponding aromatic amine and phenol derivatives under mild conditions. The yields of the products after recrysallization from acetic acid were in the order of 65-95 %. IR and 1H

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