Trans-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)styrene

95%

Reagent Code: #91000
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CAS Number 78782-27-1

science Other reagents with same CAS 78782-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.11 g/mol
Formula C₁₄H₁₉BO₂
badge Registry Numbers
MDL Number MFCD03453666
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This compound is also utilized in the development of advanced materials, such as polymers and liquid crystals, due to its ability to introduce styrene moieties into molecular frameworks. Additionally, it finds applications in the synthesis of bioactive compounds and in research focused on creating novel organic electronic materials.

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Test Parameter Specification
Appearance white to light yellow liquid or cream
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿12,540.00

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Trans-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)styrene
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This compound is also utilized in the development of advanced materials, such as polymers and liquid crystals, due to its ability to introduc

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This compound is also utilized in the development of advanced materials, such as polymers and liquid crystals, due to its ability to introduce styrene moieties into molecular frameworks. Additionally, it finds applications in the synthesis of bioactive compounds and in research focused on creating novel organic electronic materials.

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