25844-73-9

Basic information

• Product Name: 2-CHLORO-5-PHENYL-PYRAZINE
• Synonyms: 2-CHLORO-5-PHENYL-PYRAZINE;C90108
• CAS NO: 25844-73-9
• Molecular Formula: C₁₀H₇ClN₂
• Molecular Weight: 190.63
• Mol File: 25844-73-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 296.8°Cat760mmHg
• Flash Point: 161.4°C
• Appearance: /
• Density: 1.245g/cm³
• Vapor Pressure: 0.00248mmHg at 25°C
• Refractive Index: 1.593
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-CHLORO-5-PHENYL-PYRAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-5-PHENYL-PYRAZINE(25844-73-9)
• EPA Substance Registry System: 2-CHLORO-5-PHENYL-PYRAZINE(25844-73-9)

Safety Data

• Statements: 41
• Safety Statements: 26-39
• RIDADR: UN 2811 6.1 / PGIII
• Hazardous Substances Data: 25844-73-9(Hazardous Substances Data)

Usage

General Description

2-Chloro-5-phenyl-pyrazine is a chemical compound with the formula C8H6ClN2. It is a pyrazine derivative, which is a six-membered heterocyclic ring containing two nitrogen atoms in positions 1 and 4. 2-CHLORO-5-PHENYL-PYRAZINE is commonly used in the pharmaceutical and chemical industries as a building block for the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, including its antimicrobial and antifungal properties. Additionally, 2-chloro-5-phenyl-pyrazine is considered to be a promising compound for the development of new drug candidates due to its diverse biological activities and structural versatility.

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

Upstream product

• 29460-97-7 2-phenylpyrazine 
• 58861-94-2 2-phenylpyrazine 4-oxide 
• 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 
• 61578-11-8 2-chloro-5-phenylpyrazine-1-oxide 
• 58861-89-5 2-phenylpyrazine N⁽¹⁾-oxide 
• 25844-72-8 2-hydroxy-5-phenylpyrazine 

Downstream Products

• 32493-80-4 2,3-dichloro-5-phenylpyrazine 
• 76849-81-5 2-hydroxy-5-phenylpyrazine 4-oxide 
• 85093-95-4 3,5-dichloro-2-phenylpyrazine 1-oxide 
• 64163-11-7 2,6-dichloro-3-phenylpyrazine 
• 25844-72-8 2-hydroxy-5-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 
• 36971-86-5 methyl-(5-phenyl-pyrazin-2-yl)-malonic acid diethyl ester 
• 85093-93-2 2-chloro-5-phenylpyrazine 1,4-dioxide 
• 61578-12-9 2-chloro-5-phenyl-pyrazine 4-oxide 
• 61578-11-8 2-chloro-5-phenylpyrazine-1-oxide 
• 13535-13-2 2-amino-5-phenylpyrazine 
• 64163-13-9 1-hydroxy-5-phenyl-2(1H)-pyrazinone 
• 73444-23-2 Methyl-(5-phenyl-pyrazin-2-yl)-amine 

Relevant articles and documents

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. Part 10. Substitution Effect on Reaction of Pyrazine N-Oxides with Phosphoryl chloride

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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