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Catalog Number:
40242
CAS Number:
175883-62-2
4-Methoxy-3-methylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
4-Methoxy-3-methylbenzeneboronic acid
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Product Information

4-Methoxy-3-methylphenylboronic 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, which are pivotal in the formation of carbon-carbon bonds. Its unique structure, featuring a methoxy group and a methyl substituent, enhances its reactivity and selectivity, allowing for the efficient synthesis of complex organic molecules, including pharmaceuticals and agrochemicals.

Researchers and industry professionals appreciate 4-Methoxy-3-methylphenylboronic acid for its role in developing novel compounds with potential therapeutic applications. Its compatibility with various reaction conditions and substrates makes it a valuable tool in the synthesis of biologically active molecules. Additionally, its relatively simple handling and storage requirements contribute to its appeal in laboratory settings. This compound stands out among similar boronic acids due to its enhanced solubility and reactivity, making it a preferred choice for many synthetic applications.

Synonyms
4-Methoxy-3-methylbenzeneboronic acid
CAS Number
175883-62-2
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO3
Molecular Weight
165.98
MDL Number
MFCD02179464
PubChem ID
2773487
Melting Point
210 °C (Lit.)
Conditions
Store at RT
General Information
Synonyms
4-Methoxy-3-methylbenzeneboronic acid
CAS Number
175883-62-2
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO3
Molecular Weight
165.98
MDL Number
MFCD02179464
PubChem ID
2773487
Melting Point
210 °C (Lit.)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Methoxy-3-methylphenylboronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key building block in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: It is employed in medicinal chemistry for the design of boron-containing drugs, which can enhance the efficacy of treatments for diseases like cancer.
  • Bioconjugation: The unique properties of this boronic acid allow for selective binding to diols, making it useful in bioconjugation processes for creating targeted drug delivery systems.
  • Material Science: It is used in the development of advanced materials, including polymers and nanomaterials, which can have applications in electronics and sensors.
  • Analytical Chemistry: This compound is utilized in various analytical techniques, including chromatography, to improve the separation and detection of biomolecules.

Citations