(3-((Isopropoxycarbonyl)amino)phenyl)boronic acid

98%

Reagent Code: #200767
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CAS Number 1638329-69-7

science Other reagents with same CAS 1638329-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.03 g/mol
Formula C₁₀H₁₄BNO₄
badge Registry Numbers
MDL Number MFCD22375024
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The isopropoxycarbonyl-protected amine group enhances stability and solubility during reaction processes, and can be deprotected to release the free amine for further functionalization. This compound is especially useful in medicinal chemistry for building drug-like scaffolds and bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,790.00
inventory 250mg
10-20 days ฿4,220.00
inventory 5g
10-20 days ฿45,600.00
inventory 1g
10-20 days ฿14,110.00
(3-((Isopropoxycarbonyl)amino)phenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The isopropoxycarbonyl-protected amine group enhances stability and solubility during reaction processes, and can be deprotected to release the

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The isopropoxycarbonyl-protected amine group enhances stability and solubility during reaction processes, and can be deprotected to release the free amine for further functionalization. This compound is especially useful in medicinal chemistry for building drug-like scaffolds and bioactive molecules.

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