[3-(2-Propyn-1-ylcarbamoyl)phenyl]boronic acid

95%

Reagent Code: #227648
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CAS Number 874459-94-6

science Other reagents with same CAS 874459-94-6

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides under palladium catalysis. The propynylcarbamoyl moiety provides a handle for further functionalization or conjugation, making it useful in the development of bioactive molecules and functional materials. Commonly applied in medicinal chemistry for constructing drug-like scaffolds and in the preparation of boron-containing compounds for potential therapeutic use.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,030.00
250mg
10-20 days ฿3,450.00
1g
10-20 days ฿10,070.00
5g
10-20 days ฿37,310.00
[3-(2-Propyn-1-ylcarbamoyl)phenyl]boronic acid
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Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides under palladium catalysis. The propynylcarbamoyl moiety provides a handle for further functionalization or conjugation, making it useful in the development of bioactive molecules and functional materials. Commonly applied in medicinal chemistry for constructing drug-like scaffolds and in the pre

Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides under palladium catalysis. The propynylcarbamoyl moiety provides a handle for further functionalization or conjugation, making it useful in the development of bioactive molecules and functional materials. Commonly applied in medicinal chemistry for constructing drug-like scaffolds and in the preparation of boron-containing compounds for potential therapeutic use.

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