(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol

≥95%

Reagent Code: #113078
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CAS Number 1082066-29-2

science Other reagents with same CAS 1082066-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.09 g/mol
Formula C₁₃H₁₈BFO₃
badge Registry Numbers
MDL Number MFCD18732617
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the presence of the methanol group allows for further functionalization, enhancing its versatility in designing target compounds. Its application is particularly significant in medicinal chemistry for synthesizing biologically active molecules and in material science for developing organic electronic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,359.00
inventory 1g
10-20 days ฿5,121.00
inventory 250mg
10-20 days ฿2,043.00

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(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the presence of the methanol group allows for further functionalization, enhancing its versatility in designing target compo

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the presence of the methanol group allows for further functionalization, enhancing its versatility in designing target compounds. Its application is particularly significant in medicinal chemistry for synthesizing biologically active molecules and in material science for developing organic electronic materials.

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