433969-27-8 | 2-((tert-butoxycarbonylamino)methyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	>95%	in stock	$146.00	$102.00
250mg	95%	in stock	$147.00	$103.00
1g	>95%	in stock	$279.00	$195.00
5g	95%	in stock	$869.00	$608.00
10g	95%	in stock	$1,412.00	$989.00

Description

• Catalog Number: AB60795
• Chemical Name: 2-((tert-butoxycarbonylamino)methyl)phenylboronic acid
• CAS Number: 433969-27-8
• Molecular Formula: C12H18BNO4
• Molecular Weight: 251.0866
• MDL Number: MFCD05663974
• SMILES: O=C(OC(C)(C)C)NCc1ccccc1B(O)O

Computed Properties

• Complexity: 278
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 5

Upstream Synthesis Route

The compound (2-(((tert-Butoxycarbonyl)amino)methyl)phenyl)boronic acid, also known as $name$, is a versatile building block widely used in chemical synthesis. Its primary application lies in organic chemistry as a key reagent for Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, a crucial step in constructing complex organic molecules. $name$ plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and materials science due to its ability to facilitate the coupling of aryl and vinyl halides with boronic acids or esters. This selective and efficient method allows chemists to create a wide range of functionalized structures with high yields, making $name$ a valuable tool in drug discovery and development.In addition to its use in cross-coupling reactions, $name$ can also serve as a directing group for C-H activation, enabling the functionalization of aromatic compounds. This strategy offers a direct and atom-economical approach to introduce new functional groups into organic molecules, reducing the number of synthetic steps required.Overall, the application of $name$ in chemical synthesis highlights its significance in modern organic chemistry and its pivotal role in advancing the field of molecular design and synthesis.