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Catalog Number:
40030
CAS Number:
5735-41-1
2-(Hydroxymethyl)phenylboronic acid cyclic monoester
Purity:
≥ 97% (HPLC)
Synonym(s):
1,3-Dihydro-1-hydroxy-2,1-benzoxaborole
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Product Information

2-(Hydroxymethyl)phenylboronic acid cyclic monoester, also known as 1-hydroxy-3H-2,1-benzoxaborole, is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique boron-containing structure that enhances its reactivity and selectivity in various chemical reactions. Its ability to form stable complexes with diols makes it particularly valuable in the development of sensors and catalysts. Researchers have found it effective in the synthesis of biologically active molecules, including pharmaceuticals and agrochemicals, due to its favorable properties such as high stability and solubility in organic solvents.

In addition to its applications in synthetic chemistry, 2-(Hydroxymethyl)phenylboronic acid cyclic monoester is also being explored for its potential in drug delivery systems and targeted therapies. Its boron atom plays a crucial role in the design of boron neutron capture therapy (BNCT) agents, which are promising in cancer treatment. The compound's unique features, such as its ability to selectively bind to specific biomolecules, position it as a valuable tool for researchers and industry professionals looking to innovate in drug development and diagnostics.

Synonyms
1,3-Dihydro-1-hydroxy-2,1-benzoxaborole
CAS Number
5735-41-1
Purity
≥ 97% (HPLC)
Molecular Formula
C7H7BO2
Molecular Weight
133.94
MDL Number
MFCD01075677
PubChem ID
403788
Melting Point
98 - 102 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
1,3-Dihydro-1-hydroxy-2,1-benzoxaborole
CAS Number
5735-41-1
Purity
≥ 97% (HPLC)
Molecular Formula
C7H7BO2
Molecular Weight
133.94
MDL Number
MFCD01075677
PubChem ID
403788
Melting Point
98 - 102 °C
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

2-(Hydroxymethyl)phenylboronic acid cyclic monoester is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in the synthesis of boron-containing pharmaceuticals, which are known for their unique mechanisms of action against various diseases, including cancer.
  • Chemical Sensing: It is employed in the development of sensors for detecting biomolecules, providing high sensitivity and selectivity, which is essential in medical diagnostics.
  • Polymer Chemistry: The compound is used to create boron-based polymers, enhancing material properties such as strength and thermal stability, making it valuable in materials science.
  • Organic Synthesis: It serves as a versatile building block in organic synthesis, allowing chemists to create complex molecules efficiently, which is beneficial in both academic and industrial settings.
  • Bioconjugation: This chemical is utilized in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is important in drug delivery systems and targeted therapies.

Citations