Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40224
CAS Number:
313545-44-7
2-Chloro-4-ethoxyphenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
2-Chloro-4-ethoxybenzeneboronic acid
Documents
$58.39 /200MG
Pack Size Availability Price
Request Bulk Quote
Product Information

2-Chloro-4-ethoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, which is crucial in the development of targeted therapies and advanced materials. Researchers and industry professionals appreciate its stability and compatibility with various reaction conditions, enabling efficient and reliable synthesis processes.

In addition to its synthetic applications, 2-Chloro-4-ethoxyphenylboronic acid serves as a valuable reagent in the preparation of biologically active compounds. Its role in the creation of novel drug candidates highlights its importance in pharmaceutical research, particularly in the development of treatments for various diseases. The compound's ability to form stable complexes with diols further enhances its utility in sensor technology and material science. With its broad range of applications and benefits, 2-Chloro-4-ethoxyphenylboronic acid stands out as a key player in modern chemical research and development.

Synonyms
2-Chloro-4-ethoxybenzeneboronic acid
CAS Number
313545-44-7
Purity
98 - 105% (Assay by titration)
Molecular Formula
C8H10BClO3
Molecular Weight
200.43
MDL Number
MFCD02684318
PubChem ID
3539716
Melting Point
108 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Chloro-4-ethoxybenzeneboronic acid
CAS Number
313545-44-7
Purity
98 - 105% (Assay by titration)
Molecular Formula
C8H10BClO3
Molecular Weight
200.43
MDL Number
MFCD02684318
PubChem ID
3539716
Melting Point
108 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloro-4-ethoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting cancer and other diseases, enhancing the efficiency of drug discovery.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic compounds, making it valuable in creating complex molecules for research and industrial applications.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Bioconjugation: It plays a significant role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, facilitating studies in biochemistry and molecular biology.
  • Environmental Chemistry: This chemical is utilized in the detection and analysis of pollutants, aiding in environmental monitoring and ensuring compliance with safety regulations.

Citations