3-Aminocarbonylphenylboronic acid

98%

  • Product Code: 90261
  Alias:    3-Formylaminophenylboronic acid
  CAS:    351422-73-6
Molecular Weight: 164.95 g./mol Molecular Formula: H₂NCOC₆H₄BOH₂
EC Number: MDL Number: MFCD03411948
Melting Point: 232-235°C Boiling Point:
Density: Storage Condition: 2~8°C
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.
Product Specification:
Test Specification
ELEMENTAL ANALYSISCARBON 48.4-53.5
ELEMENTAL ANALYSISNITROGEN 8.1-8.9
Purity 98-100
MEILTING POINT 221-226
APPEARANCE CRYSTALLINE POWDER
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿370.00
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5.000 10-20 days ฿1,080.00
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25.000 10-20 days ฿4,880.00
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100.000 10-20 days ฿18,980.00
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3-Aminocarbonylphenylboronic acid
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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