3-Methyl-2-buten-2-ylboronic acid pinacol ester

95%

Reagent Code: #91254
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CAS Number 219488-99-0

science Other reagents with same CAS 219488-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.09 g/mol
Formula C₁₁H₂₁BO₂
inventory_2 Storage & Handling
Density 0.888 g/mL at 25℃
Storage room temperature

description Product Description

Used in organic synthesis as a key intermediate for cross-coupling reactions, particularly in Suzuki-Miyaura reactions, to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and reactivity make it suitable for constructing complex organic molecules, including natural products and bioactive compounds. Additionally, it is employed in material science for the development of organic electronic materials and polymers. Its boronate ester group ensures compatibility with various reaction conditions, enhancing its versatility in synthetic applications.

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inventory 1g
10-20 days ฿12,465.00

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3-Methyl-2-buten-2-ylboronic acid pinacol ester
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Used in organic synthesis as a key intermediate for cross-coupling reactions, particularly in Suzuki-Miyaura reactions, to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and reactivity make it suitable for constructing complex organic molecules, including natural products and bioactive compounds. Additionally, it is employed in material science for the development of organic electronic materials and polymers. Its boronate ester
Used in organic synthesis as a key intermediate for cross-coupling reactions, particularly in Suzuki-Miyaura reactions, to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and reactivity make it suitable for constructing complex organic molecules, including natural products and bioactive compounds. Additionally, it is employed in material science for the development of organic electronic materials and polymers. Its boronate ester group ensures compatibility with various reaction conditions, enhancing its versatility in synthetic applications.
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