(4-(Cyclopropylmethoxy)phenyl)boronic acid

98%

Reagent Code: #166801
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CAS Number 411229-67-9

science Other reagents with same CAS 411229-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.02 g/mol
Formula C₁₀H₁₃BO₃
badge Registry Numbers
MDL Number MFCD04039017
thermostat Physical Properties
Boiling Point 363.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl or vinyl halides, making it valuable in creating biaryl compounds found in drug candidates. The cyclopropylmethoxy moiety contributes to metabolic stability and lipophilicity, which can enhance bioavailability in medicinal chemistry applications. Commonly employed in the synthesis of potential therapeutic agents, including kinase inhibitors and anti-inflammatory compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,990.00
inventory 5g
10-20 days ฿32,890.00
inventory 250mg
10-20 days ฿3,200.00

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(4-(Cyclopropylmethoxy)phenyl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl or vinyl halides, making it valuable in creating biaryl compounds found in drug candidates. The cyclopropylmethoxy moiety contributes to metabolic stability and lipophilicity, which can enhance bioavailability in medicinal chemistry applications. Commonly employed in th

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl or vinyl halides, making it valuable in creating biaryl compounds found in drug candidates. The cyclopropylmethoxy moiety contributes to metabolic stability and lipophilicity, which can enhance bioavailability in medicinal chemistry applications. Commonly employed in the synthesis of potential therapeutic agents, including kinase inhibitors and anti-inflammatory compounds.

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