206357-78-0 | Pyridine, 3-chloro-2-(tributylstannyl)-

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$13.00	$9.00
250mg	97%	in stock	$25.00	$17.00
1g	97%	in stock	$42.00	$29.00
25g	97%	in stock	$960.00	$672.00

Description

• Catalog Number: AB17009
• Chemical Name: Pyridine, 3-chloro-2-(tributylstannyl)-
• CAS Number: 206357-78-0
• Molecular Formula: C17H30ClNSn
• Molecular Weight: 402.58079999999984
• MDL Number: MFCD10699157
• SMILES: CCCC[Sn](c1ncccc1Cl)(CCCC)CCCC

Computed Properties

• Complexity: 225
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 10

Upstream Synthesis Route

3-Chloro-2-(tributylstannyl)pyridine is a versatile compound widely used in chemical synthesis. Its ability to selectively react with various functional groups makes it a valuable tool in organic chemistry.1. Cross-Coupling Reactions: 3-Chloro-2-(tributylstannyl)pyridine is often employed as a stannylating agent in cross-coupling reactions. It reacts with various electrophiles in the presence of a suitable catalyst to form biaryl compounds. This reaction is essential in the construction of complex organic molecules and pharmaceutical intermediates.2. Synthetic Intermediates: The tributylstannyl group in this compound acts as a removable protecting group that can be selectively cleaved under mild conditions. This property makes 3-Chloro-2-(tributylstannyl)pyridine useful in the synthesis of organic molecules where temporary protection of a specific functional group is required.3. Functionalization of Pyridine Rings: The chlorine atom and tributylstannyl group in this compound allow for the selective functionalization of pyridine rings in organic molecules. This enables the introduction of various substituents at specific positions on the pyridine ring, facilitating the synthesis of diverse compounds with tailored properties.Overall, the unique reactivity of 3-Chloro-2-(tributylstannyl)pyridine makes it a valuable reagent in organic synthesis, enabling chemists to access new chemical entities and expand the scope of possibilities in the field of chemical research.