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Catalog Number:
40226
CAS Number:
135145-90-3
2,5-Dichlorophenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2,5-Dichlorobenzeneboronic acid
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Product Information

2,5-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 effectively employed 2,5-Dichlorophenylboronic acid in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds that are crucial in creating diverse organic compounds.

In addition to its applications in synthetic chemistry, this compound has shown promise in the field of materials science, particularly in the development of sensors and advanced materials due to its ability to interact with biological molecules. Its stability and reactivity make it a preferred choice for researchers looking to enhance the efficiency of their synthetic pathways. With its broad range of applications, 2,5-Dichlorophenylboronic acid stands out as a valuable tool for professionals in both academic and industrial settings.

Synonyms
2,5-Dichlorobenzeneboronic acid
CAS Number
135145-90-3
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD01863182
PubChem ID
2773371
Melting Point
150 °C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,5-Dichlorobenzeneboronic acid
CAS Number
135145-90-3
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD01863182
PubChem ID
2773371
Melting Point
150 °C (Lit.)
Appearance
White to orange 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

2,5-Dichlorophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: It plays a significant role in the design of boron-containing drugs, which can enhance the efficacy of treatments for diseases such as cancer.
  • Bioconjugation: The unique properties of this compound allow for effective bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other compounds, which is essential in biotechnology and diagnostics.
  • Materials Science: It is used in the creation of advanced materials, including polymers and nanomaterials, which have applications in electronics and renewable energy technologies.
  • Chemical Sensors: This chemical is employed in the development of sensors that can detect specific analytes, making it valuable in environmental monitoring and quality control in various industries.

Citations