2-(Hydroxymethyl)-4-(trifluoromethyl)phenylboronic acid

98%

Reagent Code: #196719
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CAS Number 1629148-48-6

science Other reagents with same CAS 1629148-48-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.95 g/mol
Formula C₈H₈BF₃O₃
badge Registry Numbers
MDL Number MFCD22574938
inventory_2 Storage & Handling
Storage Room temperature, dry

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 research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. The presence of a hydroxymethyl group allows further functionalization, such as esterification or ether formation, making it valuable in building molecular diversity. Commonly employed in the development of bioactive compounds where the trifluoromethyl group enhances metabolic stability and lipophilicity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,310.00
inventory 250mg
10-20 days ฿2,270.00
inventory 1g
10-20 days ฿6,200.00
inventory 5g
10-20 days ฿23,610.00
inventory 10g
10-20 days ฿47,190.00

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2-(Hydroxymethyl)-4-(trifluoromethyl)phenylboronic 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 research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. The presence of a hydroxymethyl group allows further functionalization, such as esterification or ether formation, making it valuable in building molecular diversity. Commonly employed in the development of bioactive compounds where

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. The presence of a hydroxymethyl group allows further functionalization, such as esterification or ether formation, making it valuable in building molecular diversity. Commonly employed in the development of bioactive compounds where the trifluoromethyl group enhances metabolic stability and lipophilicity.

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