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4-CYANO-4'-NITRODIPHENYL, also known as 4-cyano-4'-nitrodiphenylamine, is a chemical compound with the molecular formula C18H12N2O2. It is a yellow to orange crystalline powder that serves as an intermediate in the production of dyes, particularly disperse dyes. 4-CYANO-4'-NITRODIPHENYL also functions as a pigment, a UV stabilizer, and a pharmaceutical intermediate. While it is considered to have low toxicity to humans, it can cause irritation to the skin, eyes, and respiratory system upon contact or inhalation. Furthermore, it has potential environmental impacts due to its persistence in the environment and its ability to bioaccumulate in organisms.

31835-63-9

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31835-63-9 Usage

Uses

Used in Dye Production Industry:
4-CYANO-4'-NITRODIPHENYL is used as an intermediate in the production of dyes, specifically disperse dyes, for its ability to contribute to the formation of vibrant and stable colorants.
Used as a Pigment:
In the pigment industry, 4-CYANO-4'-NITRODIPHENYL is utilized for its color properties, providing a yellow to orange hue in various applications.
Used as a UV Stabilizer:
4-CYANO-4'-NITRODIPHENYL is employed as a UV stabilizer to protect materials from the damaging effects of ultraviolet radiation, thereby enhancing their durability and longevity.
Used as a Pharmaceutical Intermediate:
In the pharmaceutical industry, 4-CYANO-4'-NITRODIPHENYL is used as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 31835-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,8,3 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31835-63:
(7*3)+(6*1)+(5*8)+(4*3)+(3*5)+(2*6)+(1*3)=109
109 % 10 = 9
So 31835-63-9 is a valid CAS Registry Number.

31835-63-9SDS

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-nitrophenyl)benzonitrile

1.2 Other means of identification

Product number -
Other names p-NCC6H4C6H4NO2

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:31835-63-9 SDS

31835-63-9Relevant academic research and scientific papers

Efficient aqueous-phase Suzuki coupling of activated aryl chlorides with arylboronic acids using D-glucosamine-based dicyclohexylarylphosphine

Konovets, Anzhelika,Penciu, Alexandra,Framery, Eric,Percina, Nathalie,Goux-Henry, Catherine,Sinou, Denis

, p. 3205 - 3208 (2007/10/03)

The synthesis of a new D-glucosamine-based dicyclohexylarylphosphine has been developed. The catalytic performance of this neutral ligand is demonstrated in the Suzuki-Miyaura cross-coupling reaction between several arylboronic acids and aryl or heteroaryl chlorides.

Polymer-Assisted Solution-Phase (PASP) Suzuki Couplings Employing an Anthracene-Tagged Palladium Catalyst

Lan, Ping,Berta, Daniela,Porco Jr., John A.,South, Michael S.,Parlow, John J.

, p. 9678 - 9686 (2007/10/03)

A general method for polymer-assisted solution-phase (PASP) Suzuki reactions employing a combination of anthracene-tagged palladium catalyst and anthracene-tagged boronic acid with a polymer-supported carbonate base is reported. The anthracene-tagged catalyst allows for the easy removal of the Pd catalyst along with the dissociated phosphine ligand and phosphine oxide byproducts by sequestration through a chemoselective Diels-Alder reaction with a maleimide resin. The polymer-supported carbonate base facilitates the removal of excess boronic acid and the borane-containing byproducts present at the end of the coupling reaction. The Suzuki coupling reaction can be efficiently conducted by using combinations of the anthracene-tagged Pd catalyst, polymer-supported carbonate base, and anthracene-tagged boronic acid to yield the desired product in high purity and yield without the use of chromatography.

SYNTHESIS OF 4-ALKOXY-4'-CYANOBIPHENYLS

Ruolene, Yu. I.,Adomenas, P. V.,Adomenene, O. K.,Denis, G. I.

, p. 1192 - 1195 (2007/10/02)

A preparative method was developed for the synthesis of liquid crystals of the 4-alkoxy-4'-cyanobiphenyl group.It involves the nitration of 4-cyanobiphenyl to 4-nitro-4'-cyanobiphenyl, reduction of the latter, diazotization of the obtained 4-amino-4'-cyanobiphenyl, and alkylation of the 4-hydroxy-4'-cyanobiphenyl formed during decomposition of the diazonium salt.

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