115377-94-1 | 2-BOC-aminophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$38.00	$27.00
1g	98%	in stock	$53.00	$37.00
5g	98%	in stock	$207.00	$145.00

Description

• Catalog Number: AA21400
• Chemical Name: 2-BOC-aminophenylboronic acid
• CAS Number: 115377-94-1
• Molecular Formula: C11H16BNO4
• Molecular Weight: 237.06
• MDL Number: MFCD02179450
• SMILES: O=C(OC(C)(C)C)Nc1ccccc1B(O)O

Computed Properties

• Complexity: 265
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 4

Upstream Synthesis Route

(2-((tert-Butoxycarbonyl)amino)phenyl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block for various organic reactions. Its unique structure allows for selective functionalization and cross-coupling reactions in the synthesis of complex organic molecules. This compound serves as a crucial intermediate in the formation of biologically active compounds, pharmaceuticals, and advanced materials. Its application in Suzuki-Miyaura coupling reactions enables the formation of carbon-carbon bonds, essential for constructing diverse organic frameworks. Additionally, (2-((tert-Butoxycarbonyl)amino)phenyl)boronic acid is utilized in the preparation of boron-containing polymers and coordination complexes, further demonstrating its significance in modern synthetic chemistry. Its compatibility with a wide range of functional groups makes it a valuable tool for chemists in achieving precise and efficient transformations during organic synthesis processes.