Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
26705
CAS Number:
176528-19-1
(2,6-Dimethoxy-4-methylphenyl)boronic acid
Purity:
≥ 99% (LCMS)
Documents
$74.81 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(2,6-Dimethoxy-4-methylphenyl)boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is known 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 complex organic molecules, particularly in the synthesis of pharmaceuticals and agrochemicals. Its effectiveness in facilitating the formation of carbon-carbon bonds allows for the creation of diverse chemical structures, enhancing the efficiency of synthetic pathways.

In addition to its role in organic synthesis, (2,6-Dimethoxy-4-methylphenyl)boronic acid has shown potential in the development of sensors and materials science applications. Its ability to selectively bind to specific biomolecules opens avenues for innovative diagnostic tools and therapeutic agents. The compound's stability and reactivity make it a preferred choice for researchers looking to streamline their synthesis processes while achieving high yields. With its broad range of applications, (2,6-Dimethoxy-4-methylphenyl)boronic acid stands out as a valuable asset in both academic and industrial settings.

CAS Number
176528-19-1
Purity
≥ 99% (LCMS)
Molecular Formula
C9H13BO4
Molecular Weight
196.0
MDL Number
MFCD12198458
PubChem ID
18936507
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
176528-19-1
Purity
≥ 99% (LCMS)
Molecular Formula
C9H13BO4
Molecular Weight
196.0
MDL Number
MFCD12198458
PubChem ID
18936507
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2,6-Dimethoxy-4-methylphenyl)boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, facilitating the development of new drugs and crop protection agents.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry, thereby enabling the construction of complex molecular architectures.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, enhancing the study of biological systems.
  • Material Science: This compound is applied in the development of advanced materials, such as polymers and nanomaterials, due to its ability to participate in various chemical reactions that modify material properties.
  • Diagnostics: Its unique reactivity can be harnessed in diagnostic applications, such as the design of sensors for detecting glucose levels, offering potential benefits in diabetes management.

Citations