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Catalog Number:
40315
CAS Number:
219735-99-6
Acide 2-chloro-4-méthoxyphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-chloro-4-méthoxybenzèneboronique
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Product Information

2-Chloro-4-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized 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 enhances the synthesis of complex organic molecules, thereby streamlining the development of innovative compounds.

Additionally, 2-Chloro-4-methoxyphenylboronic acid serves as a valuable building block in the synthesis of biologically active compounds, including potential drug candidates. Its favorable reactivity profile and compatibility with various functional groups allow for diverse applications in chemical research and development. With its proven track record in enhancing synthetic efficiency, this compound is an indispensable tool for chemists aiming to push the boundaries of modern chemistry.

Synonyms
Acide 2-chloro-4-méthoxybenzèneboronique
CAS Number
219735-99-6
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C7H8BClO3
Molecular Weight
186.4
MDL Number
MFCD03411935
PubChem ID
2773330
Melting Point
202 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2-chloro-4-méthoxybenzèneboronique
CAS Number
219735-99-6
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C7H8BClO3
Molecular Weight
186.4
MDL Number
MFCD03411935
PubChem ID
2773330
Melting Point
202 °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-Chloro-4-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, enhancing drug efficacy and specificity.
  • Organic Synthesis: It is employed in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently, which is crucial for developing new materials and chemicals.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation techniques for creating targeted drug delivery systems.
  • Material Science: This compound is used in the production of boron-containing polymers, which exhibit unique properties such as enhanced thermal stability and electrical conductivity, beneficial for electronic applications.
  • Analytical Chemistry: It acts as a reagent in various analytical methods, including chromatography and mass spectrometry, aiding in the detection and quantification of biomolecules.

Citations