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"Benzenamine, 4-[[4-(trifluoromethyl)phenyl]azo]-" is an organic compound with the chemical formula C13H11F3N4. It is a derivative of aniline, featuring an azo group (-N=N-) connecting two aromatic rings, one being a trifluoromethyl-substituted phenyl group. Benzenamine, 4-[[4-(trifluoromethyl)phenyl]azo]- is known for its vibrant color and is often used as a dye or pigment in various applications. It is also referred to as 4-[(4-trifluoromethyl)phenylazo]aniline, indicating the presence of a trifluoromethyl group on the phenyl ring attached to the azo group. The compound's properties, such as its color and stability, make it valuable in industrial settings, particularly in the production of colored materials.

1961-53-1

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1961-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1961-53-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1961-53:
(6*1)+(5*9)+(4*6)+(3*1)+(2*5)+(1*3)=91
91 % 10 = 1
So 1961-53-1 is a valid CAS Registry Number.

1961-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-(trifluoromethyl)phenyl]diazenyl]aniline

1.2 Other means of identification

Product number -
Other names 4-(4-trifluoromethylphenylazo)aniline

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:1961-53-1 SDS

1961-53-1Relevant academic research and scientific papers

Pesticidal Compositions

-

Page/Page column 11, (2010/08/18)

The invention disclosed in this document is related to the field of pesticides and their use in controlling pests. A compound having the following structure is disclosed.

A photoswitchable methylene-spaced fluorinated aryl azobenzene monolayer grafted on silicon

Min, Misook,Bang, Gyeong Sook,Lee, Hyoyoung,Yu, Byung-Chan

supporting information; experimental part, p. 5232 - 5234 (2010/08/22)

Aryldiazonium-terminated methylene-spaced trifluoromethylazobenzene derivatives have been synthesized. Their self-assembled monolayers (SAMs) on a silicon surface allow for a stable and reversible molecular photoswitch.

Syntheses of new functionalized azobenzenes for potential molecular electronic devices

Yu, Byung-Chan,Shirai, Yasuhiro,Tour, James M.

, p. 10303 - 10310 (2007/10/03)

New non-symmetrical azobenzene derivatives have been synthesized as potential molecular electronic switching device candidates. The Oxone mediated oxidation of anilines provided nitroso-functionalized arenes, which were then condensed with substituted anilines to provide a series of azobenzene derivatives that could be further converted into oligo(phenylene ethynylene)s or diazonium salts. The resulting thiolacetates, thiols, or diazonium salts are capable of forming molecular layers on the surface of gold or silicon, thereby paving the way for molecular electronics testing.

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