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Catalog Number:
40293
CAS Number:
127972-02-5
Acide 5-formyl-2-méthoxyphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 5-formyl-2-méthoxybenzèneboronique
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Product Information

5-Formyl-2-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules. Its unique structure allows for the introduction of various functional groups, facilitating the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate its compatibility with a range of substrates, which enhances its utility in diverse chemical transformations.

In addition to its synthetic applications, 5-Formyl-2-methoxyphenylboronic acid has shown potential in the development of targeted therapies due to its ability to form stable complexes with biomolecules. This characteristic opens avenues for its use in drug discovery and development, particularly in the design of inhibitors for specific biological targets. With its favorable reactivity and functionalization capabilities, this compound stands out as a valuable resource for chemists and researchers aiming to innovate in their respective fields.

Synonyms
Acide 5-formyl-2-méthoxybenzèneboronique
CAS Number
127972-02-5
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 9 B O 4
Molecular Weight
179.97
MDL Number
MFCD01319044
PubChem ID
2734367
Melting Point
160 °C (lit.)
Appearance
Poudre orange à jaune à verte
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 5-formyl-2-méthoxybenzèneboronique
CAS Number
127972-02-5
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 9 B O 4
Molecular Weight
179.97
MDL Number
MFCD01319044
PubChem ID
2734367
Melting Point
160 °C (lit.)
Appearance
Poudre orange à jaune à verte
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

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

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique boronic acid functionality allows for the creation of targeted drug delivery systems, enhancing the efficacy of therapeutic agents in treating diseases.
  • Bioconjugation: The compound is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and diagnostic tools.
  • Chemical Sensors: Leveraging its reactivity, it is used in the design of chemical sensors that detect specific analytes, providing real-time monitoring in environmental and industrial applications.
  • Material Science: This chemical plays a role in the development of advanced materials, such as polymers with tailored properties, which are essential in various industrial applications.

Citations