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Catalog Number:
40304
CAS Number:
182344-13-4
3-Chloro-4-hydroxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Chloro-4-hydroxybenzeneboronic acid
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Product Information

3-Chloro-4-hydroxyphenylboronic acid is a versatile compound widely utilized in the fields of 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 structure allows for selective reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Researchers appreciate its role in the creation of biologically active compounds, including potential anti-cancer agents and other therapeutic molecules.

Moreover, 3-Chloro-4-hydroxyphenylboronic acid stands out due to its enhanced stability and reactivity compared to similar compounds, facilitating more efficient synthesis processes. Its applications extend to the development of sensors and materials in nanotechnology, where its boronic acid functionality can be exploited for glucose sensing and other biosensing applications. This compound is an invaluable tool for researchers and industry professionals seeking to innovate in drug discovery and materials science.

Synonyms
3-Chloro-4-hydroxybenzeneboronic acid
CAS Number
182344-13-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C6H6BClO3
Molecular Weight
172.37
MDL Number
MFCD09258739
PubChem ID
22125373
Appearance
White to pale yellow powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Chloro-4-hydroxybenzeneboronic acid
CAS Number
182344-13-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C6H6BClO3
Molecular Weight
172.37
MDL Number
MFCD09258739
PubChem ID
22125373
Appearance
White to pale yellow 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-Chloro-4-hydroxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in synthesizing various pharmaceuticals, particularly in developing drugs that target specific biological pathways.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Organic Synthesis: The compound serves as a versatile building block in organic synthesis, allowing chemists to create complex molecules with precision.
  • Diagnostics: It is employed in the development of diagnostic tools, particularly in assays that require specific binding interactions, improving the accuracy of disease detection.
  • Material Science: The compound is used in creating advanced materials, including polymers and coatings, that exhibit enhanced properties such as durability and chemical resistance.

Citations