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2-Phenylethane-1,1,2-tricarbonitrile is an organic compound with the chemical formula C11H7N3. It is a derivative of 2-phenylethane, where three cyano groups (-CN) are attached to the molecule. 2-phenylethane-1,1,2-tricarbonitrile is characterized by its aromatic ring structure and the presence of three nitrile functional groups, which contribute to its unique chemical properties. It is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile structure and reactivity. The compound is typically synthesized through the reaction of 2-phenylethane with cyanogen chloride or other cyanation agents. It is an important intermediate in the production of certain pharmaceuticals and can also be used as a building block in the synthesis of more complex organic molecules.

4965-21-3

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4965-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4965-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4965-21:
(6*4)+(5*9)+(4*6)+(3*5)+(2*2)+(1*1)=113
113 % 10 = 3
So 4965-21-3 is a valid CAS Registry Number.

4965-21-3SDS

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 2-phenylethane-1,1,2-tricarbonitrile

1.2 Other means of identification

Product number -
Other names 2-PHENYL-1,2-ETHATNETRICARBONITRILE

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:4965-21-3 SDS

4965-21-3Relevant academic research and scientific papers

New porphyrazine macrocycles with high viscosity-sensitive fluorescence parameters

Lermontova,Grigoryev,Shilyagina, N. Yu.,Peskova,Balalaeva,Shirmanova,Klapshina

, p. 1330 - 1338 (2016/08/10)

New tetraaryltetracyanoporphyrazines have been obtained in the form of metal complexes and free bases via template assembly of a variety of aryltricyanoethylenes as structural units of the macrocycle, and photophysical properties of the products have been

Interactions in Molecular Crystals, 127 [1]: The Different Structures in the Crystal of Twisted 1,4-Bis(tricyanovinyl)benzene as well as of Planar 1-Tricyanovinyl-benzene, Density Functional Calculations and Reduction Behaviour Studied by Cyclovoltammetry

Bock, Hans,Seitz, Wolfgang,Nagel, Norbert,Baur, Ruediger,Bats, Jan W.,Havlas, Zdenek,Claridge, Rodney F. C.

, p. 1125 - 1138 (2007/10/03)

The attempted crystal growth of 1,4-bis(tricyanovinyl)benzene dianion salts, although without success so far, has provided information of general interest. The crystal structures of the related mono and 1,4-bis(tricyanovinyl)benzene derivatives differ con

Synthesis and Trasformations of 5-Amino-2,3-dihydro-oxoles

Ciller, J. A.,Martin, M.,Quinteiro, M.,Seoano, C.,Soto, J. L.

, p. 1321 - 1331 (2007/10/02)

Treatment of α-cyanocinnamonitriles 1 with hydrogen cyanide in acetone results in the formation of 5-amino-2,3-dihydro-oxoles 3.Tricyanoethanes 2 can be obtained as intermediate compounds in a two-step process leading to the same dihydro-oxoles.Acid hydro

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