(4-(Benzylcarbamoyl)-3-chlorophenyl)boronic acid

98%

Reagent Code: #153578
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CAS Number 850589-42-3

science Other reagents with same CAS 850589-42-3

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scatter_plot Molecular Information
Weight 289.53 g/mol
Formula C₁₄H₁₃BClNO₃
badge Registry Numbers
MDL Number MFCD07363769
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables carbon-carbon bond formation, making it valuable in drug discovery and development. The presence of both a chloro and benzylcarbamoyl group allows for further functionalization or modification, enhancing its utility in creating complex molecules. Commonly applied in the preparation of bioactive compounds and potential therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,670.00
inventory 1g
10-20 days ฿7,070.00
inventory 5g
10-20 days ฿21,480.00

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(4-(Benzylcarbamoyl)-3-chlorophenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables carbon-carbon bond formation, making it valuable in drug discovery and development. The presence of both a chloro and benzylcarbamoyl group allows for further functionalization or modification, enhancing its utility in creating complex molecules. Commonly applied in the preparation of bioactive compounds and potential therapeut

Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables carbon-carbon bond formation, making it valuable in drug discovery and development. The presence of both a chloro and benzylcarbamoyl group allows for further functionalization or modification, enhancing its utility in creating complex molecules. Commonly applied in the preparation of bioactive compounds and potential therapeutic agents.

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