1206641-26-0 | 5-(Methylsulfonyl)pyridine-3-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$26.00	$19.00
250mg	97%	in stock	$49.00	$35.00

Description

• Catalog Number: AE26173
• Chemical Name: 5-(Methylsulfonyl)pyridine-3-boronic acid pinacol ester
• CAS Number: 1206641-26-0
• Molecular Formula: C12H18BNO4S
• Molecular Weight: 283.1516
• MDL Number: MFCD12198145
• SMILES: CC1(C)OB(OC1(C)C)c1cncc(c1)S(=O)(=O)C

Computed Properties

• Complexity: 427
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2

Upstream Synthesis Route

The 3-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound widely used in chemical synthesis. Its unique structure allows it to participate in a variety of reactions, making it a valuable tool for organic chemists.One of the key applications of this compound is as a functional group in cross-coupling reactions. When combined with a suitable catalyst, the 3-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine can react with a variety of electrophiles to form new carbon-carbon bonds. This makes it useful in the synthesis of pharmaceuticals, agrochemicals, and various functional materials.Additionally, this compound can be utilized as a building block in the construction of complex organic molecules. By incorporating the 3-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl 1,3,2-dioxaborolan-2-yl)pyridine moiety into a molecule, chemists can introduce specific functionalities and stereochemistry with precision, enabling the creation of diverse chemical structures for various purposes.In summary, the 3-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a valuable compound in chemical synthesis, offering unique reactivity and versatility for the creation of complex organic molecules in a controlled and efficient manner.