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Catalog Number:
40319
CAS Number:
762287-57-0
Acide 4-chloro-2-méthoxyphénylboronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 4-chloro-2-méthoxybenzèneboronique
Documents
$87.53 /200 mg
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Product Information

4-Chloro-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 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 effectiveness in facilitating the formation of carbon-carbon bonds allows for the construction of complex molecular architectures, which is crucial in drug discovery and development.

Moreover, 4-Chloro-2-methoxyphenylboronic acid exhibits excellent solubility in organic solvents, enhancing its applicability in various reaction conditions. Its selective reactivity and compatibility with a range of functional groups make it an ideal choice for chemists aiming to optimize synthetic pathways. With its proven track record in the synthesis of biologically active compounds, this boronic acid is a valuable addition to any laboratory focused on innovative research and development.

Synonyms
Acide 4-chloro-2-méthoxybenzèneboronique
CAS Number
762287-57-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C7H8BClO3
Molecular Weight
186.4
MDL Number
MFCD02684317
PubChem ID
3858606
Melting Point
134 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Boiling Point
345,4°C / 760 mmHg (Lit.)
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-chloro-2-méthoxybenzèneboronique
CAS Number
762287-57-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C7H8BClO3
Molecular Weight
186.4
MDL Number
MFCD02684317
PubChem ID
3858606
Melting Point
134 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Boiling Point
345,4°C / 760 mmHg (Lit.)
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-Chloro-2-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential for creating complex organic molecules.
  • Material Science: The compound is used in the production of advanced materials, including polymers and nanomaterials, enhancing their properties for applications in electronics and coatings.
  • Agricultural Chemistry: It plays a role in the development of agrochemicals, improving the efficacy of herbicides and pesticides, which can lead to better crop yields.
  • Bioconjugation Techniques: This chemical is utilized in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for diagnostics and therapeutic applications.

Citations