1020657-86-6 | 9-ethyl-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$44.00	$31.00
1g	95%	in stock	$80.00	$56.00
5g	95%	in stock	$273.00	$191.00
25g	95%	in stock	$1,132.00	$793.00
100g	95%	in stock	$3,403.00	$2,382.00

Description

• Catalog Number: AE24598
• Chemical Name: 9-ethyl-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole
• CAS Number: 1020657-86-6
• Molecular Formula: C20H24BNO2
• Molecular Weight: 321.2210599999999
• MDL Number: MFCD19053172
• SMILES: CCn1c2ccc(cc2c2c1cccc2)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 464
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 24
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

9-Ethyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-9H-carbazole is a versatile compound widely utilized in chemical synthesis. This compound serves as an efficient building block in the synthesis of various organic molecules due to its unique structure and reactivity. Specifically, it is commonly employed as a key intermediate in the preparation of functional materials, pharmaceuticals, and agrochemicals.In chemical synthesis, 9-Ethyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-9H-carbazole acts as a valuable precursor for introducing the carbazole moiety into target molecules. The boron-containing group in its structure facilitates Suzuki-Miyaura cross-coupling reactions, enabling the selective and efficient attachment of the carbazole unit to diverse organic frameworks. This synthetic capability makes it an essential tool for constructing complex molecular architectures with desired properties.Moreover, the presence of the ethyl group provides steric hindrance, which can influence the regioselectivity and reaction outcomes in further transformations. The tetramethyl-dioxaborolane moiety enhances the stability and compatibility of this compound in various reaction conditions, ensuring its utility in demanding synthetic protocols.Overall, the application of 9-Ethyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-9H-carbazole in chemical synthesis showcases its significance as a strategic building block for molecular design and diversification, enabling the efficient construction of novel compounds with tailored properties for a wide range of applications.