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2-BROMO-5-PHENYLPYRAZINE, with the molecular formula C10H8N2Br, is a pyrazine derivative featuring a bromine atom at the 2-position and a phenyl group at the 5-position on the pyrazine ring. This chemical compound is recognized for its diverse applications across various industries, including pharmaceuticals, agrochemicals, and the food industry.

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  • 243472-69-7 Structure
  • Basic information

    1. Product Name: 2-BROMO-5-PHENYLPYRAZINE
    2. Synonyms: 2-BROMO-5-PHENYLPYRAZINE
    3. CAS NO:243472-69-7
    4. Molecular Formula: C10H7BrN2
    5. Molecular Weight: 235.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 243472-69-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 317.79 °C at 760 mmHg
    3. Flash Point: 145.995 °C
    4. Appearance: /
    5. Density: 1.494 g/cm3
    6. Vapor Pressure: 0.001mmHg at 25°C
    7. Refractive Index: 1.612
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-BROMO-5-PHENYLPYRAZINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-BROMO-5-PHENYLPYRAZINE(243472-69-7)
    12. EPA Substance Registry System: 2-BROMO-5-PHENYLPYRAZINE(243472-69-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 243472-69-7(Hazardous Substances Data)

243472-69-7 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-BROMO-5-PHENYLPYRAZINE is utilized as a building block in the synthesis of a variety of pharmaceuticals and agrochemicals. Its unique structure contributes to the development of new compounds with potential therapeutic and pesticidal properties, enhancing the range of treatments and protections available in these fields.
Used in the Food Industry:
As a flavoring agent, 2-BROMO-5-PHENYLPYRAZINE imparts a distinctive, earthy aroma to a range of food products. Its ability to add depth and complexity to flavors makes it a valuable ingredient in the creation of unique taste profiles.
Used in Research and Industrial Applications:
2-BROMO-5-PHENYLPYRAZINE has been investigated for its potential antimicrobial and antifungal properties. This research indicates its potential use in the development of new antimicrobial agents, contributing to the fight against resistant strains of bacteria and fungi, and offering new solutions in various industrial applications where microbial control is essential.

Check Digit Verification of cas no

The CAS Registry Mumber 243472-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,4,7 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 243472-69:
(8*2)+(7*4)+(6*3)+(5*4)+(4*7)+(3*2)+(2*6)+(1*9)=137
137 % 10 = 7
So 243472-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrN2/c11-10-7-12-9(6-13-10)8-4-2-1-3-5-8/h1-7H

243472-69-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-5-phenylpyrazine

1.2 Other means of identification

Product number -
Other names Pyrazine,2-bromo-5-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:243472-69-7 SDS

243472-69-7Downstream Products

243472-69-7Relevant articles and documents

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

Sato, Nobuhiro,Narita, Nobuhiko

, p. 783 - 786 (2007/10/03)

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.

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