330793-09-4 | 3-BOC-aminophenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$6.00	$4.00
1g	96%	in stock	$7.00	$5.00
5g	96%	in stock	$31.00	$22.00
10g	96%	in stock	$60.00	$42.00

Description

• Catalog Number: AI47879
• Chemical Name: 3-BOC-aminophenylboronic acid, pinacol ester
• CAS Number: 330793-09-4
• Molecular Formula: C17H26BNO4
• Molecular Weight: 319.2036
• MDL Number: MFCD03789256
• SMILES: O=C(OC(C)(C)C)Nc1cccc(c1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 428
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 23
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4

Upstream Synthesis Route

The tert-Butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate is a valuable compound widely utilized in chemical synthesis processes. It serves as a versatile building block in organic chemistry due to its compatibility with various functional groups and its ability to undergo diverse reactions.In chemical synthesis, this compound is commonly employed as a protecting group for amines. By strategically introducing the tert-Butyl carbamate moiety to an amine compound, it effectively shields the amine functionality from unwanted reactions or undesired transformations during the synthetic pathway. This protective group can be selectively removed under specific conditions, allowing for further manipulation or functionalization of the amine group.Additionally, the presence of the 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety provides a unique handle for cross-coupling reactions, particularly in the field of palladium-catalyzed coupling reactions. This functional group enables the selective modification of the compound through Suzuki-Miyaura coupling or related transformations, facilitating the synthesis of complex organic molecules with high efficiency and selectivity.Overall, tert-Butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate plays a crucial role in chemical synthesis by enabling the protection and functionalization of amines, as well as serving as a key component in advanced synthetic strategies such as cross-coupling reactions.