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Catalog Number:
40292
CAS Number:
480424-49-5
Acide 3-formyl-2-méthoxyphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-formyl-2-méthoxybenzèneboronique
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Product Information

3-Formyl-2-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules. Its unique structure allows for the introduction of various functional groups, facilitating the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in the creation of biologically active compounds, as it can enhance the efficacy of drug candidates through structural modifications.

In addition to its synthetic applications, 3-Formyl-2-methoxyphenylboronic acid exhibits potential in the field of materials science, where it can be employed in the development of advanced polymers and nanomaterials. Its compatibility with various substrates and ease of functionalization make it a preferred choice for chemists looking to innovate in both academic and industrial settings. The compound's stability and reactivity provide significant advantages over similar boronic acids, positioning it as a key player in modern chemical research and development.

Synonyms
Acide 3-formyl-2-méthoxybenzèneboronique
CAS Number
480424-49-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 9 B O 4
Molecular Weight
179.97
MDL Number
MFCD08689486
PubChem ID
16218167
Melting Point
128 °C (lit.)
Appearance
Poudre cristalline blanche à légèrement jaune
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 3-formyl-2-méthoxybenzèneboronique
CAS Number
480424-49-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 9 B O 4
Molecular Weight
179.97
MDL Number
MFCD08689486
PubChem ID
16218167
Melting Point
128 °C (lit.)
Appearance
Poudre cristalline blanche à légèrement jaune
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

3-Formyl-2-methoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic synthesis, enabling the creation of complex molecules for pharmaceuticals and agrochemicals.
  • Drug Development: It plays a crucial role in medicinal chemistry, particularly in the development of targeted therapies for various diseases, including cancer.
  • Materials Science: The compound is used in the fabrication of advanced materials, such as polymers and nanomaterials, enhancing their properties for industrial applications.
  • Bioconjugation: It is valuable in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Sensor Technology: This chemical is applied in the development of sensors, particularly for detecting biological molecules, providing a sensitive and specific means of analysis in clinical settings.

Citations