185315-51-9

Basic information

• Product Name: 2-(5-chloropyridin-2-yl)acetonitrile
• Synonyms: 2-(5-chloropyridin-2-yl)acetonitrile;(5-Chloro-pyridin-2-yl)-acetonitrile;5-chloro-2-Pyridineacetonitrile;2-(5-Chloro-2-pyridyl)acetonitrile;2-(5-Chloropyridin-2-yl)
• CAS NO: 185315-51-9
• Molecular Formula: C7H5ClN2
• Molecular Weight: 152.581
• Mol File: 185315-51-9.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-(5-chloropyridin-2-yl)acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-chloropyridin-2-yl)acetonitrile(185315-51-9)
• EPA Substance Registry System: 2-(5-chloropyridin-2-yl)acetonitrile(185315-51-9)

Safety Data

• Hazardous Substances Data: 185315-51-9(Hazardous Substances Data)

Usage

General Description

2-(5-chloropyridin-2-yl)acetonitrile is a chemical compound with the molecular formula C7H5ClN2. It is a cyanopyridine derivative, which means it contains a nitrile group and a chloropyridine group. 2-(5-chloropyridin-2-yl)acetonitrile is commonly used in the pharmaceutical industry for the synthesis of various drugs and biologically active molecules. It is also used as a building block in organic synthesis to create more complex chemical compounds. The presence of the chloropyridine group makes 2-(5-chloropyridin-2-yl)acetonitrile a versatile and valuable intermediate in the production of a wide range of pharmaceuticals and fine chemicals.

Upstream product

• 10177-24-9 5-chloro-pyridin-2-ylmethyl chloride 
• 16110-09-1 2,5 dichloropyridine 

Relevant articles and documents

Direct access to 2-aminopyrazolo[1,5-a]pyridines via N-amination/cyclization reactions of 2-pyridineacetonitriles

We describe the straightforward synthesis of 6-substituted-2-aminopyrazolo[1,5-a]pyridines from 2-pyridineacetonitriles by N-amination with O-(mesitylsulfonyl)hydroxylamine and subsequent base-promoted cyclization. This N-amination/intramolecular cyclization reaction allows access to a variety of 6-substituted-2-aminopyrazolo[1,5-a]pyridines in a one-pot procedure, in moderate to good yields.

HETEROCYCLIC COMPOUND

The present invention provides a compound having a glucosylceramide lowering action (e.g., promoting glucosylceramide metabolism, inhibition of glucosylceramide synthesis, promoting glucosylceramide catabolism, etc.), which is expected to be useful as an

PYRAZOLOPYRIDINE DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF

A pyrazolopyridine derivative represented by the following formula (I) or a pharmacologically acceptable salt thereof exhibits a strong EP1 receptor antagonistic effect. Thus, the derivative or the pharmacologically acceptable salt is useful as