4-METHOXYCARBONYL-2-NITROPHENYLBORONIC ACID

97%

Reagent Code: #205334
label
Alias 4-methoxycarbonyl-2-nitrophenylboric acid; 4-methoxycarbonyl-2-nitrophenylboric acid; (2-nitro-4-carboxylic acid methyl ester)benzeneboric acid; 2-nitro-4-methoxycarbonyl-2-nitrophenylboric acid; 4-methoxycarbonyl-2-nitrophenylboric acid; 2-nitro-4-carboxylic acid methyl ester-2-nitrophenylboric acid
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CAS Number 85107-55-7

science Other reagents with same CAS 85107-55-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.96 g/mol
Formula C₈H₈BNO₆
thermostat Physical Properties
Melting Point 160-171°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in constructing biaryl structures found in active pharmaceutical ingredients. The nitro and ester functionalities allow further chemical modifications, enhancing its utility in multi-step syntheses. Commonly employed in the development of nitroaromatic-based drugs and functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿174.00
5g
10-20 days ฿1,140.00
50g
10-20 days ฿11,380.00
4-METHOXYCARBONYL-2-NITROPHENYLBORONIC ACID
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in constructing biaryl structures found in active pharmaceutical ingredients. The nitro and ester functionalities allow further chemical modifications, enhancing its utility in multi-step syntheses. Commonly employed in

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in constructing biaryl structures found in active pharmaceutical ingredients. The nitro and ester functionalities allow further chemical modifications, enhancing its utility in multi-step syntheses. Commonly employed in the development of nitroaromatic-based drugs and functional materials.

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