1072812-23-7 | 7-Bromoindole-2-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$85.00	$60.00
1g	98%	in stock	$229.00	$160.00
5g	98%	in stock	$760.00	$532.00
10g	98%	in stock	$1,319.00	$923.00
25g	98%	in stock	$2,625.00	$1,837.00

Description

• Catalog Number: AE20282
• Chemical Name: 7-Bromoindole-2-boronic acid pinacol ester
• CAS Number: 1072812-23-7
• Molecular Formula: C14H17BBrNO2
• Molecular Weight: 322.0053
• MDL Number: MFCD11858379
• SMILES: Brc1cccc2c1[nH]c(c2)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 347
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a versatile organic compound widely utilized in chemical synthesis processes. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials due to its unique structural features and reactivity. In chemical synthesis, 7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole acts as a valuable reagent for cross-coupling reactions, particularly in Suzuki-Miyaura coupling reactions. This compound participates in palladium-catalyzed coupling reactions with aryl halides or pseudohalides to form carbon-carbon bonds, enabling the efficient construction of complex molecular structures. Furthermore, the bromo substituent on the indole ring provides a site for further functionalization, allowing for the introduction of diverse chemical functionalities in the synthesized products. Overall, the strategic incorporation of 7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole in chemical synthesis enables the rapid and selective formation of intricate organic compounds with high synthetic efficiency.