3-Aminocarbonylphenylboronic acid

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Reagent Code: #90261
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Alias 3-Formylaminophenylboronic acid
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CAS Number 351422-73-6

science Other reagents with same CAS 351422-73-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.95 g/mol
Formula H₂NCOC₆H₄BOH₂
badge Registry Numbers
MDL Number MFCD03411948
thermostat Physical Properties
Melting Point 232-235°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

3-Aminocarbonylphenylboronic acid is widely utilized in organic synthesis, particularly as a key intermediate in the preparation of various biologically active compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a building block in the development of sensors and probes, especially for detecting sugars and other analytes, due to its ability to form reversible covalent bonds with diols. In medicinal chemistry, it is employed in the design of enzyme inhibitors and drug candidates, particularly those targeting diseases like cancer and diabetes. Its unique structure also makes it useful in material science for creating functionalized polymers and coatings.

format_list_bulleted Product Specification

Test Parameter Specification
Elemental Analysis (Carbon) 48.4-53.5
Elemental Analysis (Nitrogen) 8.1-8.9
Purity 98-100
Melting Point 221-226
Appearance Crystalline powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿370.00
inventory 25g
10-20 days ฿4,880.00
inventory 5g
10-20 days ฿1,080.00
inventory 100g
10-20 days ฿18,980.00

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3-Aminocarbonylphenylboronic acid
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3-Aminocarbonylphenylboronic acid is widely utilized in organic synthesis, particularly as a key intermediate in the preparation of various biologically active compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a building block in the development of sensors and probes, especially for detecting sugars and other analytes, due to

3-Aminocarbonylphenylboronic acid is widely utilized in organic synthesis, particularly as a key intermediate in the preparation of various biologically active compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a building block in the development of sensors and probes, especially for detecting sugars and other analytes, due to its ability to form reversible covalent bonds with diols. In medicinal chemistry, it is employed in the design of enzyme inhibitors and drug candidates, particularly those targeting diseases like cancer and diabetes. Its unique structure also makes it useful in material science for creating functionalized polymers and coatings.

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