1218790-24-9 | 1-BOC-6-chloroindole-3-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$30.00	$21.00
250mg	98%	in stock	$74.00	$52.00
5g	98%	in stock	$1,178.00	$824.00
10g	98%	in stock	$1,878.00	$1,315.00
25g	98%	in stock	$3,510.00	$2,457.00

Description

• Catalog Number: AA54559
• Chemical Name: 1-BOC-6-chloroindole-3-boronic acid, pinacol ester
• CAS Number: 1218790-24-9
• Molecular Formula: C19H25BClNO4
• Molecular Weight: 377.6701
• MDL Number: MFCD15143606
• SMILES: Clc1ccc2c(c1)n(cc2B1OC(C(O1)(C)C)(C)C)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 546
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 26
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3

Upstream Synthesis Route

The tert-Butyl 6-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate is a versatile compound commonly used in chemical synthesis processes. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural features and reactivity. In particular, it can be employed in the synthesis of pharmaceuticals, agrochemicals, and materials for advanced technology applications. The presence of the boron-containing group in this compound allows for selective cross-coupling reactions, enabling the formation of complex molecular structures with high efficiency. Additionally, the tert-butyl and chloro substituents on the indole ring provide opportunities for further functionalization through diverse chemical transformations. As a result, tert-Butyl 6-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate plays a crucial role in the development of novel compounds with enhanced properties for various industrial and research purposes.