sec-Butylboronic acid

95%

Reagent Code: #91101
label
Alias sec-butylboronic acid 2-Butylboronic acid
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CAS Number 88496-88-2

science Other reagents with same CAS 88496-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.94 g/mol
Formula C₄H₁₁BO₂
badge Registry Numbers
MDL Number MFCD06656265
thermostat Physical Properties
Melting Point 85-89 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

sec-Butylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, enabling the introduction of the sec-butyl group into target structures. It is also employed in the development of boron-containing compounds, which have applications in medicinal chemistry and drug discovery. Additionally, sec-butylboronic acid is utilized in research for studying reaction mechanisms and developing new catalytic processes. Its stability and reactivity make it a versatile reagent in various chemical transformations.

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Test Parameter Specification
Purity (Titration with NaOH) 95-105
Appearance White to yellow solid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿2,280.00
inventory 25g
10-20 days ฿10,680.00

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sec-Butylboronic acid
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sec-Butylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, enabling the introduction of the sec-butyl group into target structures. It is also employed in the development of boron-containing compounds, which h

sec-Butylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, enabling the introduction of the sec-butyl group into target structures. It is also employed in the development of boron-containing compounds, which have applications in medicinal chemistry and drug discovery. Additionally, sec-butylboronic acid is utilized in research for studying reaction mechanisms and developing new catalytic processes. Its stability and reactivity make it a versatile reagent in various chemical transformations.

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