4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
≥95%
Reagent
Code: #90298
CAS Number
126726-62-3
science Other reagents with same CAS 126726-62-3
blur_circular Chemical Specifications
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Molecular Information
Weight
168.04 g/mol
Formula
C₉H₁₇BO₂
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Registry Numbers
MDL Number
MFCD08276843
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Storage & Handling
Storage
2~8℃
description Product Description
This chemical is primarily used in organic synthesis as a versatile building block for the formation of carbon-carbon and carbon-heteroatom bonds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron reagent to facilitate the coupling of aryl or vinyl halides with various organic compounds. This enables the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, its stability and reactivity make it a preferred choice in the development of new polymers and functional materials. It is also employed in the preparation of boron-containing compounds for use in medicinal chemistry and as intermediates in the production of fine chemicals.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Purity (GC) | 95-100% |
| Appearance | Colorless to light yellow liquid |
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