17570-98-8 | 2-(Bromoacetyl)pyridine hydrobromide

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$10.00	$7.00
5g	97%	in stock	$19.00	$14.00
10g	97%	in stock	$29.00	$21.00
25g	97%	in stock	$69.00	$49.00

Description

• Catalog Number: AA94581
• Chemical Name: 2-(Bromoacetyl)pyridine hydrobromide
• CAS Number: 17570-98-8
• Molecular Formula: C7H7Br2NO
• Molecular Weight: 280.9446
• MDL Number: MFCD02181196
• SMILES: BrCC(=O)c1ccccn1.Br
• NSC Number: 73994

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2

Upstream Synthesis Route

2-(Bromoacetyl)pyridine hydrobromide is a versatile reagent commonly used in chemical synthesis for the functionalization of organic compounds. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure contains a bromoacetyl group attached to a pyridine ring, allowing for selective reactions with nucleophiles or electrophiles, depending on the synthetic goal.In chemical synthesis, 2-(Bromoacetyl)pyridine hydrobromide can be employed in the formation of carbon-carbon and carbon-heteroatom bonds through substitution, addition, or cross-coupling reactions. Its bromoacetyl moiety facilitates the introduction of the acetyl functional group into organic molecules, enabling the modification of their properties or enhancement of their biological activities. Additionally, the presence of the pyridine ring offers a platform for further derivatization, leading to the creation of structurally diverse and complex compounds.This reagent has found widespread use in medicinal chemistry for the development of novel drug candidates and in the synthesis of chemical probes for biological studies. Its ability to undergo regioselective transformations makes it a valuable tool for the construction of intricate molecular scaffolds with desired pharmacological properties. Furthermore, the unique combination of the bromoacetyl and pyridine functionalities in 2-(Bromoacetyl)pyridine hydrobromide offers synthetic chemists a powerful means to access biologically relevant structures efficiently and selectively.