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Propanedinitrile, (1-amino-2,2,2-trifluoroethylidene)-, also known as 1-amino-2,2,2-trifluoroacetonitrile, is a chemical compound with the molecular formula C3H2F3N2. It is a colorless liquid with a molecular weight of 130.05 g/mol. Propanedinitrile, (1-amino-2,2,2-trifluoroethylidene)- is characterized by the presence of a trifluoromethyl group (CF3) and an amino group (NH2) attached to a propanedinitrile backbone. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and unique properties, it is used in the preparation of various fluorinated compounds and has potential applications in the development of new materials and chemical processes.

651-68-3

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651-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651-68-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 651-68:
(5*6)+(4*5)+(3*1)+(2*6)+(1*8)=73
73 % 10 = 3
So 651-68-3 is a valid CAS Registry Number.

651-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-amino-2,2,2-trifluoroethylidene)propanedinitrile

1.2 Other means of identification

Product number -
Other names 1-Amino-1-trifluormethyl-2,2-dicyanoethylen

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:651-68-3 SDS

651-68-3Downstream Products

651-68-3Relevant academic research and scientific papers

Synthesis of 4,5-disubstituted-3-trihalomethylisothiazoles

Zawistoski, Michael P.,Decker, Shannon M.,Griffith, David A.

supporting information; experimental part, p. 7286 - 7287 (2010/03/03)

Herein, we describe the synthesis of 4,5-disubstituted-3-trihalomethylisothiazoles from trihaloacetonitriles and 2-cyanothioacetamides or 2-ethoxycarbonylthioacetamides. The reactivity of the necessary trihaloacetonitriles has a significant impact on the

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