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Catalog Number:
40124
CAS Number:
374538-03-1
Acide 2-(méthoxycarbonyl)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-(méthoxycarbonyl)benzèneboronique
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Product Information

2-(Methoxycarbonyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a methoxycarbonyl group, enhancing its reactivity and making it an excellent candidate for various coupling reactions, particularly in the synthesis of complex organic molecules. Its ability to form stable complexes with diols and other Lewis bases makes it invaluable in the development of pharmaceuticals and agrochemicals. Researchers have successfully employed this compound in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create biaryl compounds that are essential in drug discovery and development.

Additionally, 2-(Methoxycarbonyl)phenylboronic acid exhibits unique properties that facilitate its use in sensor technology and material science. Its functional groups allow for selective binding, making it suitable for applications in biosensors and environmental monitoring. The compound's stability and ease of handling further enhance its appeal in laboratory settings, providing researchers with a reliable tool for their synthetic endeavors. With its broad range of applications, this compound stands out as a key player in advancing chemical research and innovation.

Synonyms
Acide 2-(méthoxycarbonyl)benzèneboronique
CAS Number
374538-03-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 9 B O 4
Molecular Weight
179.97
MDL Number
MFCD02179452
PubChem ID
2773496
Melting Point
104 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Acide 2-(méthoxycarbonyl)benzèneboronique
CAS Number
374538-03-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 9 B O 4
Molecular Weight
179.97
MDL Number
MFCD02179452
PubChem ID
2773496
Melting Point
104 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(Methoxycarbonyl)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 creation of complex pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is extensively used in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in developing new materials and drugs.
  • Bioconjugation: The unique reactivity of this boronic acid allows for the selective modification of biomolecules, making it valuable in bioconjugation processes for drug delivery systems.
  • Sensor Development: Its ability to form complexes with diols makes it useful in the development of chemical sensors for detecting sugars and other biomolecules, which is beneficial in medical diagnostics.
  • Research in Material Science: This compound is also applied in the synthesis of functionalized polymers and materials, contributing to advancements in nanotechnology and materials engineering.

Citations