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

95%

Reagent Code: #90269
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CAS Number 214360-76-6

science Other reagents with same CAS 214360-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.07 g/mol
Formula C₁₂H₁₇BO₃
badge Registry Numbers
MDL Number MFCD02093755
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronate ester group enables efficient coupling with aryl halides, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of advanced polymers and liquid crystals due to its ability to introduce phenol functionalities into molecular structures. The compound is also utilized in the preparation of bioactive molecules and agrochemicals, where its structural features contribute to enhanced stability and reactivity.

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Test Parameter Specification
Purity (LC) 94.5-100%
Melting point 90-98
Appearance Light brown crystalline powder

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,180.00
inventory 25g
10-20 days ฿4,910.00

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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronate ester group enables efficient coupling with aryl halides, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of advanced polymers and liquid crystals due to its ability to introduce phenol functionalities into molecular structures. The compoun
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronate ester group enables efficient coupling with aryl halides, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of advanced polymers and liquid crystals due to its ability to introduce phenol functionalities into molecular structures. The compound is also utilized in the preparation of bioactive molecules and agrochemicals, where its structural features contribute to enhanced stability and reactivity.
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