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

97%

Reagent Code: #240758
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CAS Number 443776-76-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.1 g/mol
Formula C₁₃H₁₉BO₃
badge Registry Numbers
MDL Number MFCD09266196
thermostat Physical Properties
Melting Point 42-46°C
Boiling Point 363.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a building block in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of a hydroxymethyl group allows further functionalization, such as esterification or ether formation, enabling its use in multi-step syntheses. Commonly employed in the preparation of complex aromatic compounds and biaryl structures found in active pharmaceutical ingredients. Also utilized in the synthesis of polymers and organic electronic materials due to its structural versatility and reactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿790.00
inventory 10g
10-20 days ฿1,540.00
(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol
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Used primarily as a building block in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of a hydroxymethyl group allows further functionalization, such as esterification or ether formation, enabling its use in multi-step syntheses. Commonly employed in the preparation of complex aromatic compounds a

Used primarily as a building block in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of a hydroxymethyl group allows further functionalization, such as esterification or ether formation, enabling its use in multi-step syntheses. Commonly employed in the preparation of complex aromatic compounds and biaryl structures found in active pharmaceutical ingredients. Also utilized in the synthesis of polymers and organic electronic materials due to its structural versatility and reactivity.

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