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Catalog Number:
40205
CAS Number:
192182-54-0
Acide 3,5-diméthoxyphénylboronique
Purity:
≥ 98%
Synonym(s):
Acide 3,5-diméthoxybenzèneboronique
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Product Information

3,5-Dimethoxyphenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique structure, featuring two methoxy groups, enhances its solubility and reactivity, allowing for efficient coupling reactions in Suzuki cross-coupling processes. Researchers have leveraged this compound in the synthesis of biologically active molecules, including potential anti-cancer agents and other therapeutic compounds.

In addition to its applications in drug discovery, 3,5-Dimethoxyphenylboronic acid is also valuable in materials science, particularly in the development of sensors and polymers. Its ability to selectively bind to specific substrates makes it a promising candidate for creating advanced materials with tailored properties. With its broad range of applications and unique characteristics, this compound is an excellent choice for professionals seeking reliable and effective solutions in their research and development projects.

Synonyms
Acide 3,5-diméthoxybenzèneboronique
CAS Number
192182-54-0
Purity
≥ 98%
Molecular Formula
C 8 H 11 BO 4
Molecular Weight
181.98
MDL Number
MFCD03095127
PubChem ID
4374257
Melting Point
206 - 208 °C
Appearance
Solide blanc
Boiling Point
371 °C (lit.)
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3,5-diméthoxybenzèneboronique
CAS Number
192182-54-0
Purity
≥ 98%
Molecular Formula
C 8 H 11 BO 4
Molecular Weight
181.98
MDL Number
MFCD03095127
PubChem ID
4374257
Melting Point
206 - 208 °C
Appearance
Solide blanc
Boiling Point
371 °C (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

3,5-Dimethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile 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, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic structures.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it valuable in bioconjugation processes for drug delivery systems and targeted therapies.
  • Sensor Development: This compound can be employed in the creation of chemical sensors for detecting glucose and other biomolecules, benefiting the medical diagnostics field.
  • Material Science: It is utilized in the development of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings.

Citations