1000068-23-4 | 1H-Indole-1-carboxylic acid, 2-borono-4-methoxy-, 1-(1,1-dimethylethyl) ester

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$105.00	$74.00
5g	98%	in stock	$297.00	$208.00
10g	98%	in stock	$448.00	$314.00
25g	98%	in stock	$758.00	$531.00

Description

• Catalog Number: AA00142
• Chemical Name: 1H-Indole-1-carboxylic acid, 2-borono-4-methoxy-, 1-(1,1-dimethylethyl) ester
• CAS Number: 1000068-23-4
• Molecular Formula: C14H18BNO5
• Molecular Weight: 291.1074
• MDL Number: MFCD11616286
• SMILES: COc1cccc2c1cc(n2C(=O)OC(C)(C)C)B(O)O

Upstream Synthesis Route

ideal as a versatile building block in organic synthesis, (1-(tert-Butoxycarbonyl)-4-methoxy-1H-indol-2-yl)boronic acid is well-suited for a range of chemical transformations. Due to its boronic acid functionality, it serves as a valuable reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds with high efficiency and selectivity. Additionally, this compound can be utilized in the construction of complex molecular structures through palladium-catalyzed coupling reactions, facilitating the synthesis of various biologically active compounds and pharmaceutical intermediates. With its unique combination of boronic acid and indole moieties, (1-(tert-Butoxycarbonyl)-4-methoxy-1H-indol-2-yl)boronic acid offers chemists a powerful tool for designing and accessing novel organic molecules with diverse applications.