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Phenol, 2,4-bis(phenylazo)-, also known as 2,4-Bis(phenylazo)phenol or 2,4-Bis(phenylazo)phenol, is an organic compound with the chemical formula C18H14N4O. It is a derivative of phenol, where two phenylazo groups are attached to the 2 and 4 positions of the phenol molecule. Phenol, 2,4-bis(phenylazo)- is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and ether. It is primarily used as a chemical intermediate in the synthesis of various dyes and pigments, particularly those with azo structures. Due to its potential applications in the dye industry, it is important to understand its chemical properties and reactivity.

6751-05-9

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6751-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6751-05-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6751-05:
(6*6)+(5*7)+(4*5)+(3*1)+(2*0)+(1*5)=99
99 % 10 = 9
So 6751-05-9 is a valid CAS Registry Number.

6751-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis(phenylazo)-phenol

1.2 Other means of identification

Product number -
Other names 2,4-di(phenylazo)phenol

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:6751-05-9 SDS

6751-05-9Downstream Products

6751-05-9Relevant academic research and scientific papers

PHENYLAZOAMINOPYRIDINES AND THEIR DECOMPOSITION

Pasternak, Ewaryst E.,Tomasik, Piotr,Zawadzki, Wlodzimierz

, p. 767 - 774 (2007/10/02)

Three isomeric phenylazoaminopyridines were prepared and their behavior studied under the conditions of all acid catalyzed, thermal and photolytic diazoamino rearrangements.There is no case of any rearrangement taking place of the phenylazo group into the pyridine ring, but decomposition occurs.The products of the decomposition are characterized and the mechanism of their formation discussed.

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