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Catalog Number:
40178
CAS Number:
208399-66-0
Acide 4-méthoxy-2-méthylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-méthoxy-2-méthylbenzèneboronique
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Product Information

4-Methoxy-2-methylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its application in the synthesis of biologically active compounds highlights its significance in drug discovery and development.

Additionally, 4-Methoxy-2-methylphenylboronic acid serves as a key building block in the preparation of various functionalized organic molecules, enhancing the efficiency of synthetic pathways. Its favorable solubility and reactivity profile make it an attractive choice for chemists looking to streamline their processes. With its proven track record in facilitating complex chemical transformations, this compound stands out as a reliable tool for innovation in both laboratory and industrial settings.

Synonyms
Acide 4-méthoxy-2-méthylbenzèneboronique
CAS Number
208399-66-0
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD02684315
PubChem ID
2773486
Melting Point
191 °C (déc.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-méthoxy-2-méthylbenzèneboronique
CAS Number
208399-66-0
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD02684315
PubChem ID
2773486
Melting Point
191 °C (déc.)
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

4-Methoxy-2-methylphenylboronic 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.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, allowing researchers to form carbon-carbon bonds efficiently, which is crucial for creating diverse chemical libraries.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it valuable in bioconjugation techniques for drug delivery systems and targeted therapies.
  • Sensor Development: This compound is applied in the development of chemical sensors for detecting glucose levels, offering a potential advantage in diabetes management through its selectivity and sensitivity.
  • Material Science: It plays a role in the creation of advanced materials, such as polymers and nanocomposites, enhancing properties like conductivity and mechanical strength.

Citations