1211523-71-5 | 2-(2-Bromopyridin-3-yl)acetonitrile

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$79.00	$56.00
250mg	95%	in stock	$85.00	$60.00
500mg	95%	in stock	$142.00	$99.00
1g	95%	in stock	$233.00	$163.00
5g	95%	in stock	$859.00	$602.00
10g	95%	in stock	$1,317.00	$922.00

Description

• Catalog Number: AE48509
• Chemical Name: 2-(2-Bromopyridin-3-yl)acetonitrile
• CAS Number: 1211523-71-5
• Molecular Formula: C7H5BrN2
• Molecular Weight: 197.032
• MDL Number: MFCD10000072
• SMILES: Brc1ncccc1CC#N

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.5

Upstream Synthesis Route

2-(2-Bromopyridin-3-yl)acetonitrile is a versatile compound widely used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure and reactivity, this compound serves as a crucial intermediate in the synthesis of complex organic molecules.In organic synthesis, 2-(2-Bromopyridin-3-yl)acetonitrile acts as a valuable starting material for the preparation of functionalized pyridine derivatives. Its bromo-substituted pyridine moiety enables further derivatization through cross-coupling reactions such as Suzuki-Miyaura, Negishi, or Heck coupling, allowing the introduction of diverse functional groups.Additionally, the acetonitrile group in 2-(2-Bromopyridin-3-yl)acetonitrile offers synthetic versatility, serving as a site for further transformation through various chemical reactions such as nucleophilic substitution, reduction, or cyclization. This compound's ability to undergo selective modifications makes it a valuable tool for designing and synthesizing novel chemical structures with tailored properties.Furthermore, 2-(2-Bromopyridin-3-yl)acetonitrile finds applications in medicinal chemistry, where its unique structural features can be exploited for the development of potential drug candidates. By incorporating this compound into molecular frameworks, researchers can explore structure-activity relationships and optimize the pharmacological properties of lead compounds.Overall, the strategic incorporation of 2-(2-Bromopyridin-3-yl)acetonitrile in chemical syntheses enables the efficient construction of diverse molecular architectures with tailored functionalities, illustrating its significance as a versatile building block in organic chemistry.