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Benzenamine, 4-[(4-chlorophenyl)azo]-, also known as 4-(4-chlorophenylazo)aniline or C.I. 11026, is an organic compound with the chemical formula C12H10ClN3. It is a yellow crystalline solid that is soluble in organic solvents and slightly soluble in water. Benzenamine, 4-[(4-chlorophenyl)azo]- is primarily used as a dyestuff, specifically as a pigment in the color industry, and is known for its high color strength and stability. It is also used in the synthesis of other dyes and intermediates. Due to its chemical structure, it is classified as an azo compound, which is characterized by the presence of one or more azo groups (-N=N-). The compound is derived from aniline, with a 4-chlorophenylazo group attached to the 4-position of the benzene ring. It is important to note that, like many azo compounds, it may have potential health and environmental concerns, and appropriate safety measures should be taken during its handling and use.

2298-16-0

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2298-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2298-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2298-16:
(6*2)+(5*2)+(4*9)+(3*8)+(2*1)+(1*6)=90
90 % 10 = 0
So 2298-16-0 is a valid CAS Registry Number.

2298-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-chlorophenyl)diazenyl]aniline

1.2 Other means of identification

Product number -
Other names 4-Amino-4'-chlorazobenzol

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:2298-16-0 SDS

2298-16-0Relevant academic research and scientific papers

Optical Control of the GTP Affinity of K-Ras(G12C) by a Photoswitchable Inhibitor

Ge, Zhihua,Yang, Zhuojin,Liang, Jingshi,Dong, Duoling,Zhu, Mingyan

, p. 2916 - 2920 (2019/11/03)

Photocontrol of protein activity is an emerging field in biomedicine. For optical control of a mutant small GTPase K-Ras(G12C), we developed small-molecule inhibitors with photoswitchable efficacy, where one configuration binds the target protein and exer

A novel procedure to synthesize 3-chloro-1-(4a,10b-diazaphenanthrene-2-yl)- 4-phenyl azetidin-2-ones and exploration of their anti-inflammatory activity

Sharma, Manisha,Maheshwari, Arti,Bindal, Nitin

, p. E116-E120 (2013/06/04)

Some new derivatives of 3-chloro-1-(4a,10b-diazaphenanthrene-2-yl)-4-phenyl azetidin-2-one were synthesized through the reaction of N-{4-[phenyldiazenyl] phenyl}-N-[phenyl methylene] amine with 4-[phenyldiazenyl] aniline. The resulting 3-chloro-4-phenyl-1-{4-[phenyldiazenyl] phenyl} azetidin-2-one intermediate in benzene was irradiated in a Pyrex vessel with 350 nm UV light in a photochemical reactor to give the desired derivatives (4a-j). Structures of the new compounds were verified on the basis of spectral and elemental methods of analyses. Nine of the prepared compounds were tested for their anti-inflammatory effects; most of these compounds showed potent and significant results compared with indomethacin.

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