1226776-95-9

Basic information

• Product Name: 2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile
• Synonyms: 2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile;2-(5-AMinopyridin-2-yl)-2-Methylpropanenitrille;2-(5-AMino-2-pyridyl)-2-Methylpropanenitrile;2-(5-Amino-pyridin-2-yl)-2-methyl-propionitrile;5-amino-α,α-dimethyl-2-Pyridineacetonitrile;2-(5-Aminopyridin-2-yl)
• CAS NO: 1226776-95-9
• Molecular Formula: C₉H₁₁N₃
• Molecular Weight: 161.20374
• Product Categories: OLED materials,pharm chemical,electronic
• Mol File: 1226776-95-9.mol

Chemical Properties

• Boiling Point: 345.922 °C at 760 mmHg
• Flash Point: 163.008 °C
• Appearance: /
• Density: 1.111
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile(1226776-95-9)
• EPA Substance Registry System: 2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile(1226776-95-9)

Safety Data

• Hazardous Substances Data: 1226776-95-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile is used as an intermediate in the synthesis of various pharmaceuticals for its potential medicinal properties. It contributes to the development of new therapeutic agents due to its chemical structure and reactivity.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile is utilized as a building block in the creation of pesticides. Its role in this industry is to provide a foundation for the development of effective and novel agrochemicals.
Used in Research and Development:
2-(5-Aminopyridin-2-yl)-2-methylpropanenitrile is used as a research compound in laboratory settings. Its chemical reactivity and potential biological activity make it a valuable tool for scientists working on drug discovery and development, as well as for exploring its possible applications in medicine and agriculture.

Upstream product

• 1256633-31-4 2-methyl-2-(5-nitropyridin-2-yl)-propanenitrile 

Relevant articles and documents

PROCESS FOR THE PREPARATION OF SUBSTITUTED IMIDAZO[4,5-C]QUINOLINE COMPOUNDS, INTERMEDIATES AND POLYMORPHS THEREOF

The present invention relates to a process for preparation of substituted imidazo[4,5- c]quinoline compounds (the compounds of formula I as described) and intermediates thereof. The present invention also relates to polymorphs of a compound encompassed in the compound of formula I and their use in the treatment of proliferative disorders, particularly cancers.

FUSED HETEROARYLS AND THEIR USES

Provided are certain fused heteroaryls, compositions thereof and methods of use therefor.

FUSED HETEROARYLS AND THEIR USES

Provided are certain fused heteroaryls, compositions thereof and methods of use therefor.

SUBSTITUTED IMIDAZOQUINOLINE DERIVATIVES AS KINASE INHIBITORS

The present invention relates to substituted imidazo[4,5-c]quinoline derivatives, the compounds of formula (I), wherein R1 R2, R3, R4, R5, R6 and R7 are as defined in the specification, processes for their preparation, pharmaceutical compositions comprising compounds of formula (I), and their use in the treatment of diseases or disorders mediated by one or more kinases, particularly proliferative diseases or disorders such as cancer. These compounds can also be used in the treatment of inflammatory diseases and angiogenesis related disorders.

SUBSTITUTED IMIDAZOQUINOLINE DERIVATIVES

The present invention relates to substituted imidazo[4,5-c]quinoline derivatives of formula (I), wherein R1, R2 and R3 are as defined in the specification, processes for their preparation, pharmaceutical compositions comprising compounds of the present invention and their use in the treatment of diseases or disorders mediated by one or more kinases, particularly proliferative diseases or disorders such as cancer. These compounds can also be used in the treatment of inflammation and angiogenesis related disorders.