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Catalog Number:
40269
CAS Number:
67492-50-6
3,5-Dichlorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3,5-Dichlorobenzeneboronic acid
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Product Information

3,5-Dichlorophenylboronic 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 structure allows for selective functionalization, which is particularly beneficial in the synthesis of complex molecules. Researchers have leveraged its properties in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create diverse carbon-carbon bonds, facilitating the production of biologically active compounds.

In addition to its applications in synthetic chemistry, 3,5-Dichlorophenylboronic acid has shown promise in the field of materials science, where it can be used to modify surfaces and enhance the properties of polymers. Its effectiveness in targeting specific biological pathways also positions it as a valuable tool in drug discovery and development. With its robust reactivity and compatibility with various reaction conditions, this compound stands out as a reliable choice for researchers and industry professionals seeking to innovate in their respective fields.

Synonyms
3,5-Dichlorobenzeneboronic acid
CAS Number
67492-50-6
Purity
98 - 105% (Assay by titration)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD00051935
PubChem ID
2734331
Melting Point
306 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3,5-Dichlorobenzeneboronic acid
CAS Number
67492-50-6
Purity
98 - 105% (Assay by titration)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD00051935
PubChem ID
2734331
Melting Point
306 °C (Lit.)
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

3,5-Dichlorophenylboronic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound plays a crucial role in the development of various drugs, particularly in the synthesis of anti-cancer agents. Its ability to form stable complexes with certain biomolecules enhances drug efficacy.
  • Organic Synthesis: It is commonly used in Suzuki coupling reactions, which are essential for creating complex organic molecules. This application is vital in the production of agrochemicals and fine chemicals.
  • Bioconjugation: The compound is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is beneficial in diagnostics and therapeutic applications.
  • Sensor Development: Its unique properties make it suitable for developing sensors that detect specific biomolecules, aiding in environmental monitoring and medical diagnostics.
  • Material Science: In material science, it is used to modify polymers, improving their properties for applications in coatings, adhesives, and electronic materials.

Citations