1105710-32-4 | 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazol-2(3H)-one

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$232.00	$162.00
250mg	95%	in stock	$390.00	$273.00
1g	95%	in stock	$765.00	$535.00
5g	95%	in stock	$1,479.00	$1,035.00

Description

• Catalog Number: AE26392
• Chemical Name: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazol-2(3H)-one
• CAS Number: 1105710-32-4
• Molecular Formula: C13H16BNO4
• Molecular Weight: 261.0814
• MDL Number: MFCD13182073
• SMILES: O=c1[nH]c2c(o1)cc(cc2)B1OC(C(O1)(C)C)(C)C

Upstream Synthesis Route

2-Oxo-2,3-dihydrobenzo[d]oxazol-6-ylboronic Acid Pinacol Ester, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. This boronic acid pinacol ester plays a crucial role as a key building block in the formation of various organic molecules due to its unique structural properties and reactivity.One significant application of 2-Oxo-2,3-dihydrobenzo[d]oxazol-6-ylboronic Acid Pinacol Ester in chemical synthesis is its use as a coupling partner in Suzuki-Miyaura cross-coupling reactions. In this reaction, $name$ acts as a boron source, enabling the efficient formation of carbon-carbon bonds between aryl or heteroaryl halides and organic boronic acids. This versatile coupling reaction is commonly employed in the synthesis of complex organic compounds, including pharmaceuticals, agrochemicals, and materials.Furthermore, $name$ can also participate in other types of C-C and C-N bond-forming reactions, such as Heck coupling, Sonogashira coupling, and Buchwald-Hartwig amination. These diverse transformations highlight the importance of 2-Oxo-2,3-dihydrobenzo[d]oxazol-6-ylboronic Acid Pinacol Ester as a valuable tool for chemists in the construction of structurally complex molecules with precise control over regioselectivity and stereoselectivity.