1003043-34-2 | 2-Bromo-3-methylpyridine-5-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$17.00	$12.00
5g	95%	in stock	$40.00	$28.00
10g	95%	in stock	$68.00	$48.00
25g	95%	in stock	$169.00	$119.00

Description

• Catalog Number: AA01800
• Chemical Name: 2-Bromo-3-methylpyridine-5-boronic acid
• CAS Number: 1003043-34-2
• Molecular Formula: C6H7BBrNO2
• Molecular Weight: 215.8403
• MDL Number: MFCD08274468
• SMILES: OB(c1cnc(c(c1)C)Br)O

Computed Properties

• Complexity: 136
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

The (6-Bromo-5-methylpyridin-3-yl)boronic acid is a versatile compound widely utilized in chemical synthesis processes. This boronic acid derivative serves as a valuable building block in the preparation of various functionalized molecules due to its reactivity and unique structural properties.In organic synthesis, (6-Bromo-5-methylpyridin-3-yl)boronic acid acts as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aryl or vinyl halides and boronic acid derivatives. This reaction is crucial in creating complex organic structures and has broad applicability in pharmaceutical, agrochemical, and material science research.Furthermore, this boronic acid compound is utilized in the synthesis of heterocyclic compounds, which are important in medicinal chemistry and drug discovery. Its ability to participate in coupling reactions with various electrophiles allows for the efficient construction of diverse molecular architectures with specific biological activities.Overall, the (6-Bromo-5-methylpyridin-3-yl)boronic acid plays a significant role in modern organic synthesis by enabling the efficient and selective formation of new chemical bonds, facilitating the development of novel compounds with potential applications in various fields of science and technology.