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Catalog Number:
40271
CAS Number:
139962-95-1
2-Formyl-4-methoxyphenylboronic acid
Purity:
97 - 104% (Assay by titration)
Synonym(s):
2-Formyl-4-methoxybenzeneboronic acid
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Product Information

2-Formyl-4-methoxyphenylboronic 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 an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structural features, including the formyl and methoxy groups, enhance its reactivity and selectivity, allowing for the development of targeted compounds with improved efficacy.

Researchers and industry professionals can leverage 2-Formyl-4-methoxyphenylboronic acid in the design of novel materials and drug candidates. Its application extends to the synthesis of biologically active compounds, where it can facilitate the introduction of boron into molecular frameworks, thereby enhancing the properties of the final products. With its high purity and reliable performance, this compound is an invaluable asset for laboratories focused on innovative chemical research and development.

Synonyms
2-Formyl-4-methoxybenzeneboronic acid
CAS Number
139962-95-1
Purity
97 - 104% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD01319043
PubChem ID
2734365
Melting Point
161 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2-Formyl-4-methoxybenzeneboronic acid
CAS Number
139962-95-1
Purity
97 - 104% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD01319043
PubChem ID
2734365
Melting Point
161 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at 2 - 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-Formyl-4-methoxyphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in the synthesis of boron-containing pharmaceuticals, which are being explored for their unique therapeutic properties, particularly in cancer treatment.
  • Organic Synthesis: It serves as an important intermediate in organic chemistry, facilitating the creation of complex molecules through various coupling reactions, which are essential in developing new materials.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems.
  • Sensor Technology: Its properties make it suitable for developing sensors that detect specific biomolecules, providing valuable tools in diagnostics and environmental monitoring.
  • Material Science: This chemical is utilized in the development of advanced materials, including polymers and nanomaterials, which have applications in electronics and nanotechnology.

Citations