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

98%

Reagent Code: #115666
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CAS Number 1309980-11-7

science Other reagents with same CAS 1309980-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.1523 g/mol
Formula C₁₅H₂₃BO₃
badge Registry Numbers
MDL Number MFCD12405017
thermostat Physical Properties
Melting Point 64-69°C
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in developing active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it is utilized in material science for creating advanced polymers and functional materials. Its stability and reactivity under mild conditions make it a preferred choice in various industrial and academic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,138.00
inventory 250mg
10-20 days ฿2,484.00
inventory 5g
10-20 days ฿21,348.00

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2-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ol
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in developing active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it is utilized in material science for creating advanced polymer

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in developing active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it is utilized in material science for creating advanced polymers and functional materials. Its stability and reactivity under mild conditions make it a preferred choice in various industrial and academic applications.

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