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Catalog Number:
40106
CAS Number:
380430-52-4
Acide 3-(benzyloxycarbonyl)phénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-(benzyloxycarbonyl)benzèneboronique, Acide 3-carbobenzoxyphénylboronique, Acide 3-carbobenzoxybenzèneboronique
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Product Information

3-(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. Researchers appreciate its role in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds and agrochemicals. The compound's unique benzyloxycarbonyl group enhances its stability and solubility, facilitating its application in various synthetic pathways.

In addition to its synthetic utility, 3-(Benzyloxycarbonyl)phenylboronic acid serves as a valuable tool in the field of materials science, where it can be employed in the preparation of functionalized polymers and advanced materials. Its ability to participate in metal-catalyzed reactions opens avenues for creating complex molecular architectures that are crucial in drug discovery and development. With its broad range of applications and significant advantages over similar compounds, this boronic acid is a must-have for researchers and industry professionals seeking to innovate in their respective fields.

Synonyms
Acide 3-(benzyloxycarbonyl)benzèneboronique, Acide 3-carbobenzoxyphénylboronique, Acide 3-carbobenzoxybenzèneboronique
CAS Number
380430-52-4
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 14 H 13 BO 4
Molecular Weight
256.06
MDL Number
MFCD02179445
PubChem ID
2773249
Melting Point
146 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-(benzyloxycarbonyl)benzèneboronique, Acide 3-carbobenzoxyphénylboronique, Acide 3-carbobenzoxybenzèneboronique
CAS Number
380430-52-4
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 14 H 13 BO 4
Molecular Weight
256.06
MDL Number
MFCD02179445
PubChem ID
2773249
Melting Point
146 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: It plays a crucial role in medicinal chemistry, aiding in the design of boron-containing drugs that can enhance therapeutic efficacy and selectivity.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in drug delivery systems.
  • Material Science: It is applied in the development of advanced materials, such as polymers and nanomaterials, which can have improved properties for various applications.
  • Analytical Chemistry: This boronic acid derivative is utilized in sensor technology, particularly in the detection of sugars and other analytes, providing high sensitivity and specificity.

Citations