916791-07-6 | 2-Bromo-6-chloropyrazine

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$39.00	$28.00
1g	98%	in stock	$48.00	$34.00
5g	98%	in stock	$144.00	$101.00
10g	98%	in stock	$288.00	$202.00
25g	98%	in stock	$572.00	$401.00

Description

• Catalog Number: AC98477
• Chemical Name: 2-Bromo-6-chloropyrazine
• CAS Number: 916791-07-6
• Molecular Formula: C4H2BrClN2
• Molecular Weight: 193.4291
• MDL Number: MFCD08752648
• SMILES: Clc1cncc(n1)Br

Computed Properties

• Complexity: 80.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 1.6

Upstream Synthesis Route

2-Bromo-6-chloropyrazine is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-Bromo-6-chloropyrazine can undergo diverse reactions such as coupling, substitution, and addition reactions. Its functional groups make it a valuable intermediate for forming complex structures in organic molecules. Additionally, the presence of bromine and chlorine atoms provides opportunities for further derivatization and modification to tailor the compound for specific applications.This compound plays a crucial role in the development of new drugs by serving as a foundation for creating bioactive molecules. Its presence in pharmaceutical synthesis helps in enhancing the efficacy and selectivity of drug candidates. Moreover, the use of 2-Bromo-6-chloropyrazine in agrochemical synthesis contributes to the production of crop protection agents and herbicides.In summary, 2-Bromo-6-chloropyrazine serves as a fundamental building block for chemical synthesis, enabling the creation of diverse compounds with applications in the pharmaceutical, agricultural, and materials industries.

Literature

• Aminopyrazine inhibitors binding to an unusual inactive conformation of the mitotic kinase Nek2: SAR and structural characterization.

  Journal of medicinal chemistry 20101111