25844-73-9

Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-5-phenyl-pyrazine is used as a building block for the synthesis of various pharmaceuticals due to its structural versatility and potential biological activities. It serves as a key intermediate in the development of new drug candidates, contributing to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-chloro-5-phenyl-pyrazine is utilized as a building block for the synthesis of various agrochemicals. Its antimicrobial and antifungal properties make it a valuable component in the development of new pesticides and fungicides, enhancing crop protection and yield.
Used in Antimicrobial Applications:
2-Chloro-5-phenyl-pyrazine is studied for its potential antimicrobial properties, making it a candidate for the development of new antimicrobial agents. Its ability to inhibit the growth of various microorganisms can contribute to the treatment of infections and the development of new antibiotics.
Used in Antifungal Applications:
The antifungal properties of 2-chloro-5-phenyl-pyrazine have been investigated, and it is considered a promising compound for the development of new antifungal agents. Its potential to combat fungal infections can lead to the creation of novel treatments for various fungal diseases.

InChI:InChI=1/C10H7ClN2/c11-10-7-12-9(6-13-10)8-4-2-1-3-5-8/h1-7H

Upstream product

• 25844-72-8 2-hydroxy-5-phenylpyrazine 
• 58861-89-5 2-phenylpyrazine N⁽¹⁾-oxide 
• 58861-94-2 2-phenylpyrazine 4-oxide 
• 61578-11-8 2-chloro-5-phenylpyrazine-1-oxide 
• 29460-97-7 2-phenylpyrazine 
• 160315-13-9 2-acetoxy-5-phenylpyrazine 
• 1074-12-0 phenylglyoxal hydrate 
• 25844-72-8 6-phenyl-3(2H)-pyridazinone 
• 243472-80-2 2-phenyl-5-trimethylsilanyloxy-pyrazine 

Downstream Products

• 67714-61-8 dimethyl-(5-phenyl-pyrazin-2-yl)-amine 
• 25844-72-8 2-hydroxy-5-phenylpyrazine 
• 73444-23-2 Methyl-(5-phenyl-pyrazin-2-yl)-amine 
• 64163-13-9 1-hydroxy-5-phenyl-2(1H)-pyrazinone 
• 76849-81-5 2-hydroxy-5-phenylpyrazine 4-oxide 
• 13535-13-2 2-amino-5-phenylpyrazine 
• 61578-12-9 2-chloro-5-phenyl-pyrazine 4-oxide 
• 61578-11-8 2-chloro-5-phenylpyrazine-1-oxide 
• 85093-93-2 2-chloro-5-phenylpyrazine 1,4-dioxide 
• 32493-80-4 2,3-dichloro-5-phenylpyrazine 
• 85093-95-4 3,5-dichloro-2-phenylpyrazine 1-oxide 
• 64163-11-7 2,6-dichloro-3-phenylpyrazine 
• 1467061-40-0 6-chloro-5-(5-phenylpyrazin-2-yl)-1H-indole-3-carbaldehyde 
• 1078167-14-2 1-Benzoyl-3-{[(5-phenylpyrazin-2-yl)oxy]methyl}azetidine-3-carboxylic acid 

Relevant academic research and scientific papers

IMIDAZOPYRAZINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND THEIR USES AS LUCIFERINS

The present invention is in the field of bioluminescence in biology and/or medicine. In particular, the invention provides imidazopyrazine derivatives, processes for preparation thereof, and their uses as luciferins.

Studies on pyrazines. 35 [1]. An improved synthesis of bromopyrazines from hydroxypyrazines

The synthesis of bromopyrazines from hydroxypyrazines was successfully effected by the procedure via trimethylsilyloxypyrazines, the sequence of which proceeds under mild conditions and does not require the isolation of intermediate.

Novel (substituted phenyl)-1,2,4-triazolo (4,3-A)pyrazines and novel 2-hydrazino-(substituted phenyl)pyrazine intermediates

This disclosure describes novel 5-,6- and 8-(phenyl and substituted phenyl)-1,2,4-triazolo[4,3-a]pyrazines which posses utility as anxiolytic agents.

Some Reactions of Mono Substituted Pyrazine Monoxides

The reactions of the monoxides of propylpyrazine and phenylpyrazine with phosphoryl chloride or acetic anhydride were investigated.Except in the case of the reaction of 2-propylpyrazine 1-oxide with acetic anhydride, chlorination or acetoxylation occurred

2,3-Diphenyl-5-ethylpyrazine

The compound 2,3-diphenyl-5-ethyl-pyrazine, useful as a precursor in the synthesis of those compounds of the class of pyrazine, arylpyrazine, diphenylpyrazine, and cycloalkylpyrazine malonates, acetates, acetamides, and acetic acids, useful for their ultraviolet light absorption properties.