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Catalog Number:
40195
CAS Number:
352534-86-2
5-Chloro-2-ethoxyphenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
5-Chloro-2-ethoxybenzeneboronic acid
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Product Information

5-Chloro-2-ethoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for selective functionalization, which is particularly beneficial in the development of pharmaceuticals and agrochemicals. Researchers have utilized this compound in the synthesis of various biologically active molecules, showcasing its potential in drug discovery and development.

In addition to its applications in synthetic chemistry, 5-Chloro-2-ethoxyphenylboronic acid has demonstrated effectiveness in the preparation of advanced materials and polymers. Its compatibility with various substrates makes it a valuable tool for chemists looking to innovate in material science. With its favorable reactivity and functionalization capabilities, this compound stands out as a preferred choice for professionals seeking reliable and efficient solutions in their research and industrial applications.

Synonyms
5-Chloro-2-ethoxybenzeneboronic acid
CAS Number
352534-86-2
Purity
98 - 105% (Assay by titration)
Molecular Formula
C8H10BClO3
Molecular Weight
200.43
MDL Number
MFCD03427055
PubChem ID
3700836
Melting Point
124 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
5-Chloro-2-ethoxybenzeneboronic acid
CAS Number
352534-86-2
Purity
98 - 105% (Assay by titration)
Molecular Formula
C8H10BClO3
Molecular Weight
200.43
MDL Number
MFCD03427055
PubChem ID
3700836
Melting Point
124 °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

5-Chloro-2-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 in the development of drugs targeting cancer and other diseases.
  • Organic Synthesis: It is used in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry, making it valuable for creating complex organic molecules.
  • Material Science: The compound is applied in the creation of advanced materials, including polymers and nanomaterials, enhancing their properties for better performance in various applications.
  • Bioconjugation: It plays a role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in drug delivery systems and diagnostics.
  • Environmental Chemistry: This chemical is also explored in environmental applications, such as the detection and removal of pollutants, contributing to cleaner and safer ecosystems.

Citations