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Catalog Number:
40326
CAS Number:
127972-00-3
Acide 2-méthoxy-5-méthylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-méthoxy-5-méthylbenzèneboronique
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Product Information

2-Methoxy-5-methylphenylboronic acid is a versatile organoboron compound that plays a crucial role in various chemical synthesis applications. This compound is particularly valued in the field of medicinal chemistry for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers utilize this compound to facilitate the formation of carbon-carbon bonds, which is fundamental in the development of pharmaceuticals and agrochemicals. Its unique structure allows for selective reactivity, enhancing the efficiency of synthetic pathways while minimizing by-products.

In addition to its applications in organic synthesis, 2-Methoxy-5-methylphenylboronic acid is also employed in the development of sensors and materials science, where its boronic acid functionality can interact with various biological molecules. This interaction opens avenues for creating innovative diagnostic tools and targeted drug delivery systems. With its favorable properties and broad applicability, this compound stands out as a valuable asset for researchers and industry professionals seeking to advance their projects in organic synthesis and materials development.

Synonyms
Acide 2-méthoxy-5-méthylbenzèneboronique
CAS Number
127972-00-3
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD02179465
PubChem ID
2773485
Melting Point
97 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2-méthoxy-5-méthylbenzèneboronique
CAS Number
127972-00-3
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD02179465
PubChem ID
2773485
Melting Point
97 °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

2-Methoxy-5-methylphenylboronic 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.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds.
  • Material Science: The compound is applied in the development of advanced materials, including polymers and nanomaterials, enhancing their properties through boron chemistry.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in drug delivery systems.
  • Analytical Chemistry: This boronic acid derivative is utilized in sensor technology for detecting sugars and other biomolecules, providing a sensitive and selective method for analysis.

Citations