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Catalog Number:
19148
CAS Number:
196861-33-3
Acide 2-méthoxy-5-(pyridin-4-yl)phénylboronique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide 5-pyridin-4-yl-2-méthoxyphénylboronique
Documents
$201.60 /250 mg
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Product Information

2-Methoxy-5-(pyridin-4-yl)phenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a methoxy group and a pyridine moiety, enhances its reactivity and selectivity, allowing researchers to develop targeted compounds with improved efficacy.

In addition to its synthetic applications, 2-Methoxy-5-(pyridin-4-yl)phenylboronic acid has shown potential in the development of novel therapeutic agents, particularly in the treatment of cancer and other diseases. Its ability to form stable complexes with various substrates makes it an attractive choice for researchers looking to explore new pathways in drug discovery. With its favorable properties and broad applicability, this compound is an invaluable resource for professionals in the fields of chemistry and pharmaceuticals.

Synonyms
Acide 5-pyridin-4-yl-2-méthoxyphénylboronique
CAS Number
196861-33-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H12BNO3
Molecular Weight
229.04
MDL Number
MFCD06658467
PubChem ID
18476091
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide 5-pyridin-4-yl-2-méthoxyphénylboronique
CAS Number
196861-33-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H12BNO3
Molecular Weight
229.04
MDL Number
MFCD06658467
PubChem ID
18476091
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
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-(pyridin-4-yl)phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in creating targeted therapies for cancer treatment.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for forming carbon-carbon bonds in organic chemistry.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems and diagnostics.
  • Material Science: It plays a role in developing advanced materials, such as polymers and nanomaterials, which have applications in electronics and photonics.
  • Research in Catalysis: This boronic acid derivative is used in catalytic processes, offering advantages in reaction efficiency and selectivity compared to other catalysts.

Citations