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Benzoic acid, 2-[[5-(1,1-dimethylethyl)-2-hydroxyphenyl]azo]-, also known as 2-[[5-(tert-butyl)-2-hydroxyphenyl]azo]benzoic acid, is an organic compound with the chemical formula C17H18N2O3. It is a derivative of benzoic acid, featuring an azo group (-N=N-) connecting a 2-hydroxyphenyl ring with a tert-butyl group to the benzoic acid backbone. Benzoic acid, 2-[[5-(1,1-dimethylethyl)-2-hydroxyphenyl]azo]- is often used as a colorant or dye in various applications, such as in the textile and plastics industries, due to its ability to impart color. It is also known for its potential use as a UV stabilizer in polymers, helping to protect materials from the degrading effects of ultraviolet light. The compound's chemical structure endows it with specific properties that make it suitable for these applications, although its use must be carefully managed due to potential environmental and health concerns associated with the release of azo dyes.

4870-44-4

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4870-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4870-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4870-44:
(6*4)+(5*8)+(4*7)+(3*0)+(2*4)+(1*4)=104
104 % 10 = 4
So 4870-44-4 is a valid CAS Registry Number.

4870-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(3-tert-butyl-6-oxocyclohexa-2,4-dien-1-ylidene)hydrazinyl]benzoic acid

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

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More Details:4870-44-4 SDS

4870-44-4Downstream Products

4870-44-4Relevant academic research and scientific papers

Dibutyltin(IV) complexes containing arylazobenzoate ligands: Chemistry, in vitro cytotoxic effects on human tumor cell lines and mode of interaction with some enzymes

Basu Baul, Tushar S.,Paul, Anup,Pellerito, Lorenzo,Scopelliti, Michelangelo,Singh, Palwinder,Verma, Pooja,Duthie, Andrew,De Vos, Dick,Tiekink, Edward R.T.

, p. 285 - 299 (2011)

Dibutyltin(IV) complexes of composition Bu2Sn (LH)2, where LH is a carboxylate residue derived from 2-[(E)- (5-tert-butyl-2- hydroxyphenyl)diazenyl]benzoate (L1H) with water molecule (1), 4-[(E)-(5-tert-butyl-2-hydroxyphen

Molecular basis of the interaction of novel tributyltin(IV) 2/4-[(E)-2-(aryl)-1-diazenyl]benzoates endowed with an improved cytotoxic profile: Synthesis, structure, biological efficacy and QSAR studies

Basu Baul, Tushar S.,Paul, Anup,Pellerito, Lorenzo,Scopelliti, Michelangelo,Pellerito, Claudia,Singh, Palwinder,Verma, Pooja,Duthie, Andrew,de Vos, Dick,Verma, Rajeshwar P.,Englert, Ulli

scheme or table, p. 950 - 966 (2011/12/04)

A series of tributyltin(IV) complexes based on 2/4-[(E)-2-(aryl)-1-diazenyl]benzoate ligands was synthesized, wherein the position of the carboxylate and aryl substituents (methyl, tert-butyl and hydroxyl) varies. The complexes, Bu3SnL1-4

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