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4-(Phenylazo)benzoic acid ethyl ester is an organic compound with the chemical formula C15H14N2O2. It is a derivative of benzoic acid, featuring an azo group (-N=N-) connecting two phenyl rings. This yellow crystalline solid is soluble in organic solvents and is commonly used as a chemical intermediate in the synthesis of dyes and pigments. The compound is also known for its potential applications in analytical chemistry as a reagent for the detection of certain metal ions. Its molecular structure and properties make it a valuable component in the development of colorants for various industries, including textiles, plastics, and printing inks.

7508-68-1

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7508-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7508-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7508-68:
(6*7)+(5*5)+(4*0)+(3*8)+(2*6)+(1*8)=111
111 % 10 = 1
So 7508-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H14N2O2/c1-2-19-15(18)12-8-10-14(11-9-12)17-16-13-6-4-3-5-7-13/h3-11H,2H2,1H3/b17-16+

7508-68-1SDS

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 ethyl 4-phenyldiazenylbenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-(phenylazo)-,ethyl ester

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:7508-68-1 SDS

7508-68-1Relevant academic research and scientific papers

Functionalized Lanthanide(III) Complexes Constructed from Azobenzene Derivative and β-Diketone Ligands: Luminescent, Magnetic, and Reversible Trans-to-Cis Photoisomerization Properties

Lin, Li-Rong,Tang, Hui-Hui,Wang, Yun-Guang,Wang, Xuan,Fang, Xue-Ming,Ma, Li-Hua

, p. 3889 - 3900 (2017/04/10)

The coordination ability of ligands functionalized by azobenzene was manipulated, and two novel chelating ligands, (E)-4-(phenyldiazenyl)-N,N-bis(pyridin-2-ylmethyl) benzohydrazide (C25H22N6O, PBPM) and (E)-4-((4-(dimethyl

Highly efficient synthesis of azos catalyzed by the common metal copper (0) through oxidative coupling reactions

Wang, Jiaqing,He, Jing,Zhi, Cong,Luo, Bin,Li, Xinming,Pan, Yue,Cao, Xueqin,Gu, Hongwei

, p. 16607 - 16611 (2014/05/06)

A facile and efficient approach to synthesize symmetric, asymmetric and bridged aromatic azo compounds (AAzos) from aromatic amines was developed by using red copper as catalyst. Despite numerous efforts towards the catalytic synthesis of symmetric and asymmetric AAzos derivatives, most reactions present certain drawbacks inhibiting their industrial applications, such as laborious multi-step processes, harsh reaction conditions and expensive reagents. And the synthesis of bridged azos had low yields before. With the presence of ammonium bromide as co-catalyst, pyridine as a ligand and molecular dioxygen as a sole oxidative reagent, red copper, a common and abundant metal in nature, exhibited unexpected catalytic activity towards the preparation of AAzos in high yields via one-step reaction, making this catalyst an attractive candidate for industrial and synthetic applications.

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