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Catalog Number:
40333
CAS Number:
361543-99-9
4-Methoxy-2,6-dimethylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
4-Methoxy-2,6-dimethylbenzeneboronic acid
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Product Information

4-Methoxy-2,6-dimethylphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Its unique structure, featuring a methoxy group and two methyl substituents, enhances its reactivity and selectivity, allowing researchers to create complex molecules with precision.

In the pharmaceutical industry, 4-Methoxy-2,6-dimethylphenylboronic acid is utilized in the development of various bioactive compounds, including potential drug candidates. Its application extends to the synthesis of agrochemicals and materials science, where it aids in the development of innovative materials with tailored properties. Researchers appreciate its ease of use and compatibility with various reaction conditions, making it a preferred choice for both academic and industrial applications. With its significant role in advancing chemical research and development, this compound stands out as a key tool for professionals seeking to enhance their synthetic methodologies.

Synonyms
4-Methoxy-2,6-dimethylbenzeneboronic acid
CAS Number
361543-99-9
Purity
≥ 98% (HPLC)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD03452755
PubChem ID
3716303
Melting Point
175 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Methoxy-2,6-dimethylbenzeneboronic acid
CAS Number
361543-99-9
Purity
≥ 98% (HPLC)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD03452755
PubChem ID
3716303
Melting Point
175 °C (Lit.)
Appearance
White to off-white crystalline powder
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-2,6-dimethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the formation of carbon-carbon bonds, which is essential for creating complex organic structures.
  • Pharmaceutical Development: It plays a significant role in drug discovery, particularly in the development of boron-containing pharmaceuticals, which can enhance the efficacy and selectivity of therapeutic agents.
  • Material Science: This chemical is used in the development of advanced materials, including polymers and composites, which benefit from its unique properties to improve strength and durability.
  • Chemical Sensors: Its boronic acid functionality allows for the detection of sugars and other biomolecules, making it valuable in the creation of sensitive chemical sensors for biomedical applications.
  • Cross-Coupling Reactions: It is an effective reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of biaryl compounds, important in agrochemicals and pharmaceuticals.

Citations