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2-AMINO-5-BROMO-6-METHYLPYRAZINE is a chemical compound with the molecular formula C5H6BrN3, characterized as a brominated derivative of pyrazine, a six-membered aromatic heterocycle containing two nitrogen atoms. It is known for its strong, savory, and slightly earthy aroma, which makes it a valuable component in the flavoring industry.

74290-69-0

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74290-69-0 Usage

Uses

Used in Flavoring Industry:
2-AMINO-5-BROMO-6-METHYLPYRAZINE is used as a flavoring agent for its distinctive strong, savory, and slightly earthy aroma, contributing to the enhancement of taste profiles in various food and beverage products.
Used in Pharmaceutical Research:
2-AMINO-5-BROMO-6-METHYLPYRAZINE is studied for its potential pharmacological activities, including its anti-cancer properties, making it a candidate for further research and development in the pharmaceutical industry.
Used in Anti-Microbial Applications:
2-AMINO-5-BROMO-6-METHYLPYRAZINE has also been investigated for its anti-microbial properties, suggesting its possible use in applications requiring microbial control, such as in the development of antimicrobial agents or treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 74290-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,9 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74290-69:
(7*7)+(6*4)+(5*2)+(4*9)+(3*0)+(2*6)+(1*9)=140
140 % 10 = 0
So 74290-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H6BrN3/c1-3-5(6)8-2-4(7)9-3/h2H,1H3,(H2,7,9)

74290-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-5-bromo-6-methylpyrazine

1.2 Other means of identification

Product number -
Other names 5-bromo-6-methylpyrazin-2-amine

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:74290-69-0 SDS

74290-69-0Relevant academic research and scientific papers

ANTIDIABETIC BICYCLIC COMPOUNDS

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, (2019/06/09)

Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-co

Substituted pyrazoloquinazolinones and pyrroloquinazolinones as allosteric modulators of group II metabotropic glutamate receptors

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Paragraph 02222, (2014/01/07)

The present invention relates to the pyrazoloquinazolinone and pyrroloquinazolinone derivatives of the general formula (I), as well as pharmaceutical compositions containing them, and their use in the treatment and/or prophylaxis of conditions associated with altered glutamatergic signalling and/or functions, and/or conditions which can be affected by alteration of glutamate level or signalling in mammals, in particular their use in the treatment and/or prophylaxis of acute and chronic neurological and/or psychiatric disorders.

SUBSTITUTED PYRAZOLOQUINAZOLINONES AND PYRROLOQUINAZOLINONES AS ALLOSTERIC MODULATORS OF GROUP II METABOTROPIC GLUTAMATE RECEPTORS

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Page/Page column 86, (2014/01/07)

The present invention relates to the pyrazoloquinazolinone and pyrroloquinazolinone derivatives of the general formula (I), as well as pharmaceutical compositions containing them, and their use in the treatment and/or prophylaxis of conditions associated with altered glutamatergic signalling and/or functions, and/or conditions which can be affected by alteration of glutamate level or signalling in mammals, in particular their use in the treatment and/or prophylaxis of acute and chronic neurological and/or psychiatric disorders.

Studies on Pyrazines. 6. A Facile Separation Method for a Mixture of the Isomeric 2-Amino-3,5, and 6-methylpyrazines

Sato, Nobuhiro

, p. 143 - 147 (2007/10/02)

This paper describes a facile separation method for a mixture of the isomeric aminomethylpyrazines by two-stage processes.Thus the mixture of aminomethylpyrazines was converted into that of the aminobromomethylpyrazines, which could be separated by chromatography on silica gel.Each of the bromopyrazines was hydrogenated to regenerate the original aminopyrazine as a pure form.

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