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Phenol, 4-[(4-aminophenyl)amino]-, also known as 4-[(4-aminophenyl)amino]phenol or 4,4'-diaminophenol, is an organic compound with the chemical formula C12H12N2O. It is a derivative of phenol, featuring two amino groups attached to the para positions of the phenol ring. Phenol, 4-[(4-aminophenyl)amino]- is a white or slightly yellow crystalline solid that is soluble in water, alcohol, and ether. It is primarily used as an intermediate in the synthesis of various dyes, pigments, and pharmaceuticals, such as the production of azo dyes and the antiseptic agent, proflavine. Due to its chemical structure, it exhibits a range of properties, including reactivity with electrophiles and nucleophiles, and it is also known for its ability to form complexes with metal ions.

6358-03-8

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6358-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6358-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6358-03:
(6*6)+(5*3)+(4*5)+(3*8)+(2*0)+(1*3)=98
98 % 10 = 8
So 6358-03-8 is a valid CAS Registry Number.

6358-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-aminoanilino)phenol

1.2 Other means of identification

Product number -
Other names 4-hydroxy-4'-aminodiphenylamine

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:6358-03-8 SDS

6358-03-8Relevant academic research and scientific papers

Design, synthesis and antitumor activity of novel cis-furoquinoline derivatives

Li, Jie,Pei, Shuchen,Zhu, Yingxi,Wu, Jianbo,Chen, Yin,Zhang, Weiyu,Wu, Yong

experimental part, p. 379 - 388 (2012/07/03)

A series of novel cis-furoquinoline derivatives was synthesized and tested for their antitumor activities in vitro against HepG2 cells, Lu-04 cells and Leu02 cells to evaluate structure-activity relationships. Assay-based antiproliferative activity study revealed that several compounds had significant effects on cytotoxicity, among which compounds 2f, 2l, 2q were found to be the most active compounds. Above all, compounds 2f, 2l, 2q would be potential anticancer agents which deserved further research.

Molecular switch based on a biologically important redox reaction

Yan, Ping,Holman, Michael W.,Robustelli, Paul,Chowdhury, Arindam,Ishak, Fady I.,Adams, David M.

, p. 130 - 137 (2007/10/03)

Building on our earlier report of a single-molecule probe,1 we show how biologically important redox centers, nicotinamide and quinone, incorporated into a fluorophore-spacer-receptor molecular structure, form redox active molecular switches, w

Reaction product of a rosin acid and an antidegradant

-

, (2008/06/13)

There is disclosed a reaction product of a rosin acid and a polyfunctional compound having at least one functional group capable of reacting with a carboxylic acid functionality and another functional group having antidegradant properties. The reaction products of this invention can be used as antidegradants in polymeric compositions and lubricating oil compositions.

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