n-Propylboronic acid

98%

Reagent Code: #91160
label
Alias n-Propylboronic Acid Propylboronic acid
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CAS Number 17745-45-8

science Other reagents with same CAS 17745-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 87.91 g/mol
Formula C₃H₉BO₂
badge Registry Numbers
EC Number 000-000-0
MDL Number MFCD01074564
thermostat Physical Properties
Melting Point 105-108°C
inventory_2 Storage & Handling
Storage 2~8°C, dry, sealed

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create carbon-carbon bonds. It serves as a key reagent in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing complex organic molecules. Also employed in the development of boron-based drugs and as an intermediate in fine chemical manufacturing. Its stability and reactivity make it a preferred choice in various catalytic processes.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 105-110
Purity (Neutralization Titration) 97.5-102%
Appearance White to off-white solid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿330.00
inventory 5g
10-20 days ฿620.00
inventory 25g
10-20 days ฿2,580.00
inventory 100g
10-20 days ฿8,910.00

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n-Propylboronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create carbon-carbon bonds. It serves as a key reagent in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing complex organic molecules. Also employed in the development of boron-based drugs and as an intermediate in fine chemical manufacturing. Its stability and reactivity make it a preferred c

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create carbon-carbon bonds. It serves as a key reagent in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing complex organic molecules. Also employed in the development of boron-based drugs and as an intermediate in fine chemical manufacturing. Its stability and reactivity make it a preferred choice in various catalytic processes.

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