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2,2'-BIPYRIDINE-3,3'-DICARBONITRILE, also known as 3,3'-dicyano-2,2'-bipyridine, is a chemical compound belonging to the bipyridine family. It features two pyridine rings connected by a carbon-carbon bond at the 3 and 3' positions, with cyano (CN) groups attached to both carbon atoms. 2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is recognized for its strong and stable complex formation with transition metal ions, making it a valuable ligand in the development of new materials for various applications.

136869-49-3

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136869-49-3 Usage

Uses

Used in Organic Synthesis:
2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is used as a key intermediate in organic synthesis for the creation of various chemical compounds due to its ability to form stable complexes with metal ions.
Used in Coordination Chemistry:
In the field of coordination chemistry, 2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is used as a ligand for the formation of coordination polymers and metal-organic frameworks. Its strong binding affinity with transition metal ions contributes to the development of materials with unique properties.
Used in Catalysis:
2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is utilized as a catalyst or catalyst precursor in various chemical reactions. The complexes formed with metal ions can act as efficient catalysts, enhancing the rate of reactions in industrial processes.
Used in Sensing:
2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is used in the development of sensing materials. The metal complexes of 2,2'-BIPYRIDINE-3,3'-DICARBONITRILE can exhibit selective binding or responsive changes, making them suitable for detecting specific analytes or environmental conditions.
Used in Molecular Recognition:
2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is employed in molecular recognition processes, where its complexes with metal ions can selectively interact with target molecules, which is crucial in fields like drug design and diagnostics.
Used in Pharmaceutical Compound Design:
In the pharmaceutical industry, 2,2'-BIPYRIDINE-3,3'-DICARBONITRILE is used as a building block for designing new pharmaceutical compounds. Its potential biological activities and versatile chemistry make it a promising candidate for creating novel therapeutic agents.
Each application highlights a different aspect of 2,2'-BIPYRIDINE-3,3'-DICARBONITRILE's utility, ranging from its role in chemical synthesis to its potential in creating advanced materials and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 136869-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136869-49:
(8*1)+(7*3)+(6*6)+(5*8)+(4*6)+(3*9)+(2*4)+(1*9)=173
173 % 10 = 3
So 136869-49-3 is a valid CAS Registry Number.

136869-49-3SDS

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 2,2-Bipyridine-3,3-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 2-(3-cyanopyridin-2-yl)pyridine-3-carbonitrile

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:136869-49-3 SDS

136869-49-3Upstream product

136869-49-3Relevant academic research and scientific papers

A Model for the Attack of a Nucleophile on a Nitrile Group: The X-Ray Crystal Structure of 2,2'-Bipyridine-3,3'-dicarbonitrile

Baxter, Paul N. W.,Connor, Joseph A.,Povey, David C.,Wallis, John D.

, p. 1135 - 1137 (2007/10/02)

From analysis of the geometry of the attractive intramolecular interactions between the pyridine N atoms and the nitrile C atoms in title compound 2 it is proposed that the most favoured direction of approach of a nucleophile to an sp C(N) makes an angle of at least 108 deg to the triple bond.

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