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Catalog Number:
16612
CAS Number:
59016-93-2
Acide 4-(hydroxyméthyl)phénylboronique
Purity:
≥ 99 % (dosage)
Synonym(s):
(4-boronophényl)méthanol
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Product Information

4-(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 in the synthesis of complex organic molecules. Researchers often leverage this compound in the preparation of biologically active compounds, including those with potential applications in cancer therapy and other therapeutic areas.

In addition to its synthetic utility, 4-(Hydroxymethyl)phenylboronic acid serves as a critical building block in the development of sensors and materials, particularly in the field of biosensing. Its ability to selectively bind to specific biomolecules opens avenues for innovative diagnostic tools. The compound's favorable properties, such as high stability and ease of functionalization, position it as a preferred choice for professionals seeking reliable and effective solutions in their research and development projects.

Synonyms
(4-boronophényl)méthanol
CAS Number
59016-93-2
Purity
≥ 99 % (dosage)
Molecular Formula
C 7 H 9 B O 3
Molecular Weight
151.96
MDL Number
MFCD00792672
PubChem ID
2734706
Melting Point
251-256 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
(4-boronophényl)méthanol
CAS Number
59016-93-2
Purity
≥ 99 % (dosage)
Molecular Formula
C 7 H 9 B O 3
Molecular Weight
151.96
MDL Number
MFCD00792672
PubChem ID
2734706
Melting Point
251-256 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents due to its ability to interact with biological targets.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Sensor Technology: The compound is employed in the creation of sensors for detecting glucose levels, making it valuable in diabetes management and research.
  • Organic Electronics: It finds applications in organic electronic devices, such as organic light-emitting diodes (OLEDs), due to its favorable electronic properties.
  • Polymer Chemistry: This chemical is used in the synthesis of boron-containing polymers, which have unique properties beneficial in materials science and engineering applications.

Citations