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Catalog Number:
40164
CAS Number:
192804-36-7
4-(Benzyloxycarbonylamino)phenylboronic acid
Purity:
≥ 98% (HPLC)
Documents
$95.94 /1G
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Product Information

4-(Benzyloxycarbonylamino)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form reversible covalent bonds with diols, making it an essential building block in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the selective modification of biomolecules, which is particularly valuable in drug discovery and development. Researchers have leveraged this compound in the synthesis of protease inhibitors and other therapeutic agents, showcasing its potential in combating diseases such as cancer and diabetes.

In addition to its applications in medicinal chemistry, 4-(Benzyloxycarbonylamino)phenylboronic acid serves as a key reagent in cross-coupling reactions, including Suzuki-Miyaura coupling, which is fundamental in the creation of complex organic molecules. Its high reactivity and selectivity make it a preferred choice among chemists looking to enhance the efficiency of their synthetic pathways. The compound's stability and ease of handling further contribute to its appeal in both academic and industrial settings, ensuring that it meets the rigorous demands of modern chemical research.

CAS Number
192804-36-7
Purity
≥ 98% (HPLC)
Molecular Formula
C14H14BNO4
Molecular Weight
271.08
MDL Number
MFCD02093055
PubChem ID
2773322
Melting Point
169 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
CAS Number
192804-36-7
Purity
≥ 98% (HPLC)
Molecular Formula
C14H14BNO4
Molecular Weight
271.08
MDL Number
MFCD02093055
PubChem ID
2773322
Melting Point
169 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(Benzyloxycarbonylamino)phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of boronic acid-based pharmaceuticals, particularly in the development of protease inhibitors used in cancer therapy.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other compounds, enhancing drug delivery systems and targeted therapies.
  • Diagnostics: The compound is used in the creation of diagnostic tools, such as sensors for detecting glucose levels, which is vital for diabetes management.
  • Material Science: In the field of material science, it contributes to the development of advanced polymers and materials with specific properties, such as improved mechanical strength and thermal stability.
  • Chemical Research: It plays a significant role in various chemical reactions and studies, particularly in the field of organometallic chemistry, aiding researchers in understanding reaction mechanisms and developing new catalysts.

Citations