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2-Amino-5-bromo-3-methylpyrazine, a pyrazine derivative with the molecular formula C5H6BrN3, is a chemical compound known for its strong, roasted, and meaty odor. It is widely used in the food and fragrance industries as a flavoring agent and aroma compound, particularly in smoked and grilled meat flavors, coffee, and cocoa products, to enhance the savory and roasted notes in food products. Additionally, it has potential anti-inflammatory and antitumor properties, making it a subject of interest in pharmaceutical research.

74290-67-8

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74290-67-8 Usage

Uses

Used in Food Industry:
2-Amino-5-bromo-3-methylpyrazine is used as a flavoring agent for its strong, roasted, and meaty odor, enhancing the savory and roasted notes in food products such as smoked and grilled meats, coffee, and cocoa.
Used in Fragrance Industry:
In the fragrance industry, 2-Amino-5-bromo-3-methylpyrazine is used as an aroma compound to create complex and rich scents, contributing to the depth and character of various fragrances.
Used in Pharmaceutical Research:
2-Amino-5-bromo-3-methylpyrazine is used as a subject of interest in pharmaceutical research due to its potential anti-inflammatory and antitumor properties, with the aim of developing new therapeutic agents for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 74290-67-8 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 74290-67:
(7*7)+(6*4)+(5*2)+(4*9)+(3*0)+(2*6)+(1*7)=138
138 % 10 = 8
So 74290-67-8 is a valid CAS Registry Number.

74290-67-8SDS

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-3-methylpyrazine

1.2 Other means of identification

Product number -
Other names 5-bromo-3-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:74290-67-8 SDS

74290-67-8Upstream product

74290-67-8Relevant academic research and scientific papers

Selectfluor-promoted regioselective chlorination/bromination of 2-aminopyridines and 2-aminodiazines using LiCl/LiBr

Hu, Jiao,Zhou, Gang,Tian, Yawei,Zhao, Xiaoming

supporting information, p. 6342 - 6345 (2019/07/10)

Using LiCl as a chlorine source, the chlorination of 2-aminopyridines or 2-aminodiazines in the presence of Selectfluor and DMF is established under mild conditions. This method gives chlorinated pyridines or diazines in good to high yields with high regioselectivities. Also, this method is extended to the bromination of 2-aminopyridines or 2-aminodiazines by using LiBr. The regioselectivity of the chlorination reaction is strongly dependent upon the substituent pattern in either the 2-aminopyridines or 2-aminodiazines. The synthesis of Buparlisib from chlorinated pyridines was explored. A study of the mechanism revealed that this chlorination occurs via either a pyridine or diazine radical process.

N-heterocyclyl sulphonamide derivatives and their use as endothelin antagonists

-

, (2008/06/13)

The invention concerns pharmaceutically useful N-heterocyclyl sulphonamide derivatives, their pharmaceutically acceptable salts, processes for their manufacture, their use for antagonising one or more actions of endothelin in a human or other warm-blooded animal, their use in methods of treatment of diseases or medical conditions in which elevated or abnormal levels of endothelin play a significant causative role.

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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