3-Aminophenylboronic acid hydrochloride

98%

Reagent Code: #90191
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Alias 3-Aminophenyl borate hydrochloride
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CAS Number 85006-23-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.41 g/mol
Formula H₂NC₆H₄BOH₂HCl
badge Registry Numbers
EC Number 285-052-4
MDL Number MFCD00191748
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis, it serves as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are crucial for creating carbon-carbon bonds in drug development. Additionally, it is employed in the design of sensors and diagnostic agents due to its ability to interact with diols and sugars, making it valuable in glucose sensing applications. The compound also finds use in material science for modifying surfaces and creating functionalized polymers. Its versatility in chemical reactions and binding properties makes it a valuable tool in both research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Loss on Drying 0-0.5
Purity (HPLC) 98-100
Purity (Neutralization Titration) 97.5-102.5
Appearance white to grey to light-brown powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿750.00
inventory 5g
10-20 days ฿3,120.00
inventory 25g
10-20 days ฿11,650.00
3-Aminophenylboronic acid hydrochloride
Used primarily in organic synthesis, it serves as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are crucial for creating carbon-carbon bonds in drug development. Additionally, it is employed in the design of sensors and diagnostic agents due to its ability to interact with diols and sugars, making it valuable in glucose sensing applications. The compound also finds use in material science for modifying surfaces and creating functionalized polymers. Its versatility in chemical reactions and binding properties makes it a valuable tool in both research and industrial applications.
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