59489-32-6

Basic information

• Product Name: 5-chloro-2,3-diMethylpyrazine
• Synonyms: 5-chloro-2,3-diMethylpyrazine;2-Chloro-5,6-dimethylpyrazine
• CAS NO: 59489-32-6
• Molecular Formula: C6H7ClN2
• Molecular Weight: 142.58618
• Mol File: 59489-32-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 81℃ (18 Torr)
• Flash Point: 90.3±11.5℃
• Appearance: /
• Density: 1.184±0.06 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 5-chloro-2,3-diMethylpyrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-2,3-diMethylpyrazine(59489-32-6)
• EPA Substance Registry System: 5-chloro-2,3-diMethylpyrazine(59489-32-6)

Safety Data

• RIDADR: UN1993
• Hazardous Substances Data: 59489-32-6(Hazardous Substances Data)

Usage

General Description

5-Chloro-2,3-dimethylpyrazine is a chemical compound with the molecular formula C6H7ClN2. It is a pyrazine derivative with a chloro group and two methyl groups attached to the pyrazine ring. 5-chloro-2,3-diMethylpyrazine is commonly used in the flavor and fragrance industry, where it is added to various products to provide a pungent, roasted, and nutty aroma. It is also found in natural sources like roasted coffee, cocoa, and cooked meat, contributing to their characteristic smell and taste. Additionally, 5-chloro-2,3-dimethylpyrazine has been studied for its potential as an anti-cancer agent, with research showing promising results in inhibiting the growth of certain cancer cells. However, further research is needed to fully understand its mechanism of action and its potential as a therapeutic agent.

Upstream product

• 5910-89-4 2,3-dimethylpyrazine 
• 65464-21-3 2,3-dimethyl-1,4-diazine N-oxide 
• 2302-39-8 4,5-dimethylimidazole 
• 67-66-3 chloroform 
• 57229-36-4 2,3-Dimethyl-5-hydroxypyrazine 

Downstream Products

• 32493-79-1 5,6-Dichloro-2,3-dimethylpyrazine 
• 1252906-06-1 2,3-dimethyl-5-[(phenylmethyl)oxy]pyrazine 
• 57229-36-4 2,3-Dimethyl-5-hydroxypyrazine 

Relevant articles and documents

NOVEL COMPOUNDS WITH A 3A-AZABICYCLO [4.1.0] HEPTANE CORE ACTING ON OREXIN RECEPTORS

This invention relates to azabicyclo[4.1.0]hept-4-yl derivatives and their use as pharmaceuticals.

SPIRO CONDENSED PIPERIDNES AS MODULATORS OF MUSCARINIC RECEPTORS

The present invention relates to modulators of muscarnic receptors of formula (I). The present invention also provides impositions comprising such modulators, and methods therewith for treating muscarinic receptor mediated diseases.

Reactions of Halogenomethanes in the Vapor Phase. Part 4. The Reactions of Imidazoles with Chloroform at 550 deg C, and a Comparison with their Liquid-phase Reactions with Trichloroacetate Ion or Hexachloroacetone and Base

1-Unsubstituted imidazoles and chloroform at 550 deg C in a flow system give mainly 5-chloropyrimidines, together with 4-chloropyrimidines and chloropyrazines.The effects of methyl substituents on the ratio of products is considered.The liquid-phase reactions of 2-methyl- and 2,4,5-trimethyl-imidazole under conditions in which dichlorocarbene is said to be formed in basic or neutral conditions were studied, and compared with the gas-phase reactions with chloroform.