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Catalog Number:
40107
CAS Number:
184000-11-1
Acide 4-(benzyloxycarbonyl)phénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-(benzyloxycarbonyl)benzèneboronique, Acide 4-carbobenzoxyphénylboronique, Acide 4-carbobenzoxybenzèneboronique
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Product Information

4-(Benzyloxycarbonyl)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 stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for the selective functionalization of aromatic compounds, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of biologically active molecules, particularly in the creation of complex natural products and drug candidates.

The compound's applications extend to materials science, where it is employed in the development of advanced polymers and nanomaterials. Its ability to act as a building block in the formation of boron-containing compounds enhances the properties of materials, making them suitable for various applications, including sensors and catalysts. With its high reactivity and specificity, 4-(Benzyloxycarbonyl)phenylboronic acid stands out as a valuable tool for chemists aiming to innovate in both research and industrial settings.

Synonyms
Acide 4-(benzyloxycarbonyl)benzèneboronique, Acide 4-carbobenzoxyphénylboronique, Acide 4-carbobenzoxybenzèneboronique
CAS Number
184000-11-1
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 14 H 13 BO 4
Molecular Weight
256.06
MDL Number
MFCD02179442
PubChem ID
2773251
Melting Point
192 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 4-(benzyloxycarbonyl)benzèneboronique, Acide 4-carbobenzoxyphénylboronique, Acide 4-carbobenzoxybenzèneboronique
CAS Number
184000-11-1
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 14 H 13 BO 4
Molecular Weight
256.06
MDL Number
MFCD02179442
PubChem ID
2773251
Melting Point
192 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies.
  • Organic Synthesis: It is employed in cross-coupling reactions, which are essential for creating complex organic molecules, making it valuable in both academic and industrial laboratories.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other compounds, enhancing the functionality of drug delivery systems and diagnostic tools.
  • Material Science: It plays a role in the development of advanced materials, including polymers that require specific chemical functionalities for improved performance.
  • Analytical Chemistry: This chemical is utilized in the preparation of boronic acid derivatives, which are important for the detection and quantification of sugars and other biomolecules in various samples.

Citations