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Catalog Number:
40217
CAS Number:
908142-03-0
3-(Hydroxymethyl)-4-methoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-(Hydroxymethyl)-4-methoxybenzeneboronic acid
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Product Information

3-(Hydroxymethyl)-4-methoxyphenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique hydroxymethyl and methoxy functional groups enhance its reactivity and selectivity, allowing for efficient coupling reactions in the synthesis of complex organic molecules. Researchers have successfully employed this compound in the preparation of biologically active compounds, including potential anticancer agents and inhibitors for various enzymatic processes.

In addition to its applications in drug discovery, 3-(Hydroxymethyl)-4-methoxyphenylboronic acid serves as a valuable tool in materials science, particularly in the development of boron-containing polymers and sensors. Its ability to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, further expands its utility in creating advanced materials with tailored properties. With its favorable characteristics and broad applicability, this compound is an excellent choice for researchers and industry professionals seeking reliable solutions for their synthetic challenges.

Synonyms
3-(Hydroxymethyl)-4-methoxybenzeneboronic acid
CAS Number
908142-03-0
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD14155851
PubChem ID
53407782
Appearance
White to light yellow crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-(Hydroxymethyl)-4-methoxybenzeneboronic acid
CAS Number
908142-03-0
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD14155851
PubChem ID
53407782
Appearance
White to light 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

3-(Hydroxymethyl)-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 can enhance drug efficacy and selectivity in targeting specific biological pathways.
  • Bioconjugation: Its boronic acid functionality allows for the selective attachment to diols in biomolecules, making it valuable in creating targeted drug delivery systems and diagnostics.
  • Organic Synthesis: It serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of agrochemicals and fine chemicals.
  • Research in Material Science: The compound is used in the development of new materials, such as polymers with enhanced properties, due to its ability to form stable complexes with various substrates.
  • Analytical Chemistry: It is employed in the detection and quantification of biomolecules, providing a reliable method for monitoring biological processes in research and clinical settings.

Citations