1126522-69-7 | 9-Phenyl-9h-carbazole-3-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$6.00	$5.00
5g	96%	in stock	$25.00	$17.00
10g	96%	in stock	$43.00	$30.00
25g	96%	in stock	$55.00	$38.00
100g	96%	in stock	$179.00	$125.00
500g	96%	in stock	$892.00	$624.00

Description

• Catalog Number: AB53197
• Chemical Name: 9-Phenyl-9h-carbazole-3-boronic acid pinacol ester
• CAS Number: 1126522-69-7
• Molecular Formula: C24H24BNO2
• Molecular Weight: 369.2639
• MDL Number: MFCD16621140
• SMILES: CC1(C)OB(OC1(C)C)c1ccc2c(c1)c1ccccc1n2c1ccccc1

Computed Properties

• Complexity: 557
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 28
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole, also known as $name$, is a versatile compound that finds diverse applications in chemical synthesis. This particular molecule is commonly used as a key building block in the creation of organic materials, pharmaceuticals, and agrochemicals. Due to its unique structure and reactivity, $name$ serves as an essential intermediate in various synthetic pathways, enabling the production of complex organic molecules with high efficiency and precision. In particular, the boron-containing moiety in $name$ facilitates cross-coupling reactions, making it a valuable tool in the synthesis of substituted carbazoles and related compounds. Furthermore, the presence of the tetramethyl groups enhances the regioselectivity and stability of the compound, making it an ideal candidate for challenging synthetic transformations. Overall, the application of 9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole in chemical synthesis is integral to the development of new molecules with potential applications in various industries.