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Benzoic acid, 4-[(4-methoxyphenyl)azo]-, also known as 4-(4-methoxyphenylazo)benzoic acid, is an organic compound with the chemical formula C14H13N2O3. It is a derivative of benzoic acid, featuring an azo group (-N=N-) attached to the 4-position of the benzene ring, and a methoxy group (-OCH3) on the 4-position of the phenyl ring connected to the azo group. Benzoic acid, 4-[(4-methoxyphenyl)azo]- is often used as a colorant or dye in various applications, such as in the textile and printing industries, due to its ability to impart color. It is also found in some azo pigments and can be used in the synthesis of other organic compounds. The compound is typically synthesized through a diazotization reaction, where a primary aromatic amine is reacted with nitrous acid to form a diazonium salt, which then couples with the appropriate phenol to form the azo compound.

3517-20-2

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3517-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3517-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3517-20:
(6*3)+(5*5)+(4*1)+(3*7)+(2*2)+(1*0)=72
72 % 10 = 2
So 3517-20-2 is a valid CAS Registry Number.

3517-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-methoxyphenyl)diazenyl]benzoic acid

1.2 Other means of identification

Product number -
Other names 4'-methoxyazobenzene-4-carboxylic acid

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:3517-20-2 SDS

3517-20-2Relevant academic research and scientific papers

A Twist-Bend Nematic (NTB) Phase of Chiral Materials

Gorecka, Ewa,Vaupoti, Nataa,Zep, Anna,Pociecha, Damian,Yoshioka, Jun,Yamamoto, Jun,Takezoe, Hideo

, p. 10155 - 10159 (2015/09/01)

New chiral dimers consisting of a rod-like and cholesterol mesogenic units are reported to form a chiral twist-bend nematic phase (NTB) with heliconical structure. The compressibility of the NTB phase made of bent dimers was found to be as large as in smectic phases, which is consistent with the nanoperiodic structure of the NTB phase. The atomic force microscopy observations in chiral bent dimers revealed a periodicity of about 50 nm, which is significantly larger than the one reported previously for non-chiral compounds (ca. 10 nm).

Bulge-like asymmetric heterodye clustering in DNA duplex results in efficient quenching of background emission based on the maximized excitonic interaction

Fujii, Taiga,Hara, Yuichi,Osawa, Takuya,Kashida, Hiromu,Liang, Xingguo,Yoshida, Yasuko,Asanuma, Hiroyuki

supporting information; experimental part, p. 10865 - 10872 (2012/09/21)

Asymmetric dye clusters with a single fluorophore (Cy3) and multiple quenchers (4′-methylthioazobenzene-4-carboxylate, methyl red, and 4′-dimethylamino-2-nitroazobenzene-4-carboxylate) were prepared. The dye and one-to-five quenchers were tethered through

Stable holographic gratings with small-molecular trisazobenzene derivatives

Kreger, Klaus,Wolfer, Pascal,Audorff, Hubert,Kador, Lothar,Stingelin-Stutzmann, Natalie,Smith, Paul,Schmidt, Hans-Werner

supporting information; experimental part, p. 509 - 516 (2010/03/25)

We present a series of small-molecular trisazobenzene chromophores, including, for instance, 1,3,5-tris{[4-[4-[(4-cyanophenyl)azo]phenoxy]butyryl] amino}benzene that feature a remarkably stable light-induced orientation in initially amorphous thin-film ar

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