3-Quinolinecarbonitrile, 2-amino-4-methyl-

3-Quinolinecarbonitrile, 2-amino-4-methyl- - Names and Identifiers

Name	3-Quinolinecarbonitrile, 2-amino-4-methyl-
Synonyms	2-Amino-4-methyl-3-quinolinecarbonitrile 2-AMINO-4-METHYL-QUINOLINE-3-CARBONITRILE 2-amino-4-methyl-quinoline-3-carbonitrile 3-Quinolinecarbonitrile, 2-amino-4-methyl-
CAS	28448-11-5

3-Quinolinecarbonitrile, 2-amino-4-methyl- - Physico-chemical Properties

Molecular Formula	C11H9N3
Molar Mass	183.21
Storage Condition	2-8°C

3-Quinolinecarbonitrile, 2-amino-4-methyl- - Risk and Safety

Safety Description	24/25 - Avoid contact with skin and eyes.
HS Code	29334900

3-Quinolinecarbonitrile, 2-amino-4-methyl- - Introduction

3-Quinolinecarbonitrile, 2-amino-4-methyl-(3-Quinolinecarbonitrile, 2-amino-4-methyl-), chemical formula C11H10N2, is an organic compound. The following is a description of its nature, use, preparation and safety information:

Nature:
-Appearance: 3-Quinolinecarbonitrile, 2-amino-4-methyl-is a pale yellow solid.
-Melting point: Approximately 217-220 ° C.
-Solubility: Soluble in chloroform and acetone, slightly soluble in acid and ethanol.

Use:
-Chemical synthesis: It can be used as an important intermediate in organic synthesis and used to synthesize other organic compounds.
-drug research: Due to its unique chemical structure, 3-Quinolinecarbonitrile, 2-amino-4-methyl-has certain potential in drug research and may have antiviral, the application value of anti-cancer and so on.

Method:
3-quinolinecarbonitrile, 2-amino-4-methyl-have many synthesis methods, and the following are commonly used:
-Schiff base condensation of quinoline: by introducing cyano and amino groups into quinoline, and then Schiff base condensation reaction with appropriate amine compounds, and finally adding methylating reagent to obtain the target product.
-Other methods include catalytic hydrogenation reaction, coupling reaction, etc.

Safety Information:
- 3-Quinolinecarbonitrile, 2-amino-4-methyl-has low toxicity, but it still needs to comply with the safety regulations of laboratory operation.
-When handling this compound, wear appropriate personal protective equipment, such as laboratory gloves and protective glasses.
-Avoid inhaling dust or contact with skin and eyes. In case of accidental contact or inhalation, rinse immediately with water and seek medical help.
-During use and storage, keep away from fire sources and high temperature environments to prevent fires and explosions.
-In addition, waste-producing organisms should be disposed of in accordance with the laws and regulations of different regions, following the principles of environmental protection.

Last Update：2024-04-09 20:52:54