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Catalog Number:
16575
CAS Number:
87199-15-3
3-(Hydroxymethyl)phenylboronic acid
Purity:
≥ 99%
Synonym(s):
(3-Boronophenyl)methanol, 3-(Hydroxymethyl)benzeneboronic acid
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Product Information

3-(Hydroxymethyl)phenylboronic 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 group enhances its reactivity, allowing for efficient coupling reactions, particularly in the synthesis of complex organic molecules. Researchers often leverage this compound in the preparation of biologically active compounds, including potential anti-cancer agents and other therapeutic molecules.

In addition to its applications in drug development, 3-(Hydroxymethyl)phenylboronic acid is also employed in materials science for the creation of functionalized polymers and sensors. Its ability to participate in Suzuki-Miyaura cross-coupling reactions further underscores its importance in the field of organic electronics and nanotechnology. With its favorable properties and broad applicability, this compound stands out as a valuable tool for researchers and industry professionals seeking to innovate and enhance their projects.

Synonyms
(3-Boronophenyl)methanol, 3-(Hydroxymethyl)benzeneboronic acid
CAS Number
87199-15-3
Purity
≥ 99%
Molecular Formula
C7H9BO3
Molecular Weight
151.96
MDL Number
MFCD01317846
PubChem ID
2734662
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
(3-Boronophenyl)methanol, 3-(Hydroxymethyl)benzeneboronic acid
CAS Number
87199-15-3
Purity
≥ 99%
Molecular Formula
C7H9BO3
Molecular Weight
151.96
MDL Number
MFCD01317846
PubChem ID
2734662
Appearance
White to off-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

3-(Hydroxymethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Drug Development: It plays a crucial role in medicinal chemistry, particularly in the design of boron-containing pharmaceuticals, which can enhance drug efficacy and selectivity.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in developing targeted therapies and diagnostics.
  • Sensor Technology: It is applied in the development of chemical sensors, particularly for detecting glucose levels, making it valuable in diabetes management and monitoring.
  • Polymer Chemistry: The compound is utilized in creating boron-containing polymers, which can exhibit unique properties such as improved thermal stability and mechanical strength, beneficial in various industrial applications.

Citations