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Catalog Number:
40270
CAS Number:
139962-97-3
4-Benzyloxy-2-formylphenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
4-Benzyloxy-2-formylbenzeneboronic acid
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$88.93 /200MG
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Product Information

4-Benzyloxy-2-formylphenylboronic acid is a versatile compound known for its unique boronic acid functionality, making it an essential building block in organic synthesis and medicinal chemistry. This compound features a benzyloxy group that enhances its reactivity and solubility, facilitating its use in various applications such as the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to form reversible covalent bonds with diols makes it particularly valuable in the synthesis of complex molecules, including glycosylated compounds and other biologically active substances.

Researchers and industry professionals can leverage 4-Benzyloxy-2-formylphenylboronic acid in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, to create carbon-carbon bonds efficiently. This compound's stability and reactivity profile allow for the development of targeted drug delivery systems and the synthesis of novel compounds with potential therapeutic applications. Its unique properties not only streamline synthetic pathways but also enhance the overall yield and purity of the final products, making it a preferred choice for chemists seeking reliable and effective reagents.

Synonyms
4-Benzyloxy-2-formylbenzeneboronic acid
CAS Number
139962-97-3
Purity
98 - 105% (Assay by titration)
Molecular Formula
C14H13BO4
Molecular Weight
256.06
MDL Number
MFCD02179486
PubChem ID
3827645
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Benzyloxy-2-formylbenzeneboronic acid
CAS Number
139962-97-3
Purity
98 - 105% (Assay by titration)
Molecular Formula
C14H13BO4
Molecular Weight
256.06
MDL Number
MFCD02179486
PubChem ID
3827645
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-Benzyloxy-2-formylphenylboronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in organic synthesis, facilitating the creation of complex molecules through cross-coupling reactions.
  • Drug Development: Its unique boronic acid functionality makes it valuable in the design of pharmaceuticals, particularly in developing inhibitors for various biological targets.
  • Material Science: The compound can be used in the fabrication of advanced materials, such as polymers and nanomaterials, enhancing properties like conductivity and mechanical strength.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other compounds, which is crucial for developing biosensors and targeted drug delivery systems.
  • Analytical Chemistry: This chemical is utilized in analytical methods for detecting and quantifying specific compounds, particularly in environmental and biological samples, improving sensitivity and selectivity.

Citations