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Catalog Number:
24607
CAS Number:
16419-60-6
2-Methylphenylboronic acid
Purity:
≥ 98%
Synonym(s):
o-Tolylboronic acid
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Product Information

2-Methylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued 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 create complex organic molecules, including pharmaceuticals and agrochemicals. Its application extends to the development of sensors and materials, where it plays a critical role in the detection of sugars and other biomolecules due to its selective binding capabilities.

The compound's ease of use and effectiveness in various chemical transformations make it a preferred choice for synthetic chemists. With its favorable reactivity profile, 2-Methylphenylboronic acid stands out among similar compounds, offering enhanced yields and selectivity in reactions. Whether in academic research or industrial applications, this compound provides significant advantages, enabling the efficient development of innovative solutions in chemistry.

Synonyms
o-Tolylboronic acid
CAS Number
16419-60-6
Purity
≥ 98%
Molecular Formula
C7H9BO2
Molecular Weight
135.96
MDL Number
MFCD00093526
PubChem ID
2733267
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
o-Tolylboronic acid
CAS Number
16419-60-6
Purity
≥ 98%
Molecular Formula
C7H9BO2
Molecular Weight
135.96
MDL Number
MFCD00093526
PubChem ID
2733267
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Methylphenylboronic 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 development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a significant role in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, thus enhancing efficiency in chemical manufacturing.
  • Sensor Development: The chemical is used in the creation of sensors for detecting sugars and other biomolecules, benefiting the food industry and medical diagnostics by providing accurate and rapid results.
  • Drug Delivery Systems: Its properties allow for the design of targeted drug delivery systems, improving the efficacy of treatments by ensuring that medications reach their intended sites in the body.
  • Material Science: 2-Methylphenylboronic acid is utilized in the development of advanced materials, including polymers and nanomaterials, which can lead to innovations in electronics and renewable energy technologies.

Citations