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Catalog Number:
40202
CAS Number:
871329-83-8
4-Ethoxy-3-(trifluoromethyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Ethoxy-3-(trifluoromethyl)benzeneboronic acid
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$87.53 /200MG
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Product Information

4-Ethoxy-3-(trifluoromethyl)phenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its unique trifluoromethyl group, which enhances its reactivity and selectivity in cross-coupling reactions, particularly in Suzuki-Miyaura coupling. Researchers and industry professionals can leverage this compound for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its ability to form stable complexes with various substrates makes it an invaluable tool in the development of targeted therapies and innovative materials.

The practical applications of 4-Ethoxy-3-(trifluoromethyl)phenylboronic acid extend to the fields of drug discovery and materials science. For instance, it can be utilized in the development of new anti-cancer agents or in the creation of functionalized polymers. Its distinctive properties, such as enhanced solubility and stability, provide significant advantages over similar compounds, making it a preferred choice for researchers seeking efficient and effective solutions in their projects.

Synonyms
4-Ethoxy-3-(trifluoromethyl)benzeneboronic acid
CAS Number
871329-83-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H10BF3O3
Molecular Weight
233.98
MDL Number
MFCD07363789
PubChem ID
44558184
Melting Point
200 - 205 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Ethoxy-3-(trifluoromethyl)benzeneboronic acid
CAS Number
871329-83-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H10BF3O3
Molecular Weight
233.98
MDL Number
MFCD07363789
PubChem ID
44558184
Melting Point
200 - 205 °C
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

4-Ethoxy-3-(trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, allowing researchers to create carbon-carbon bonds efficiently, which is essential in creating diverse chemical libraries.
  • Fluorinated Compounds: The trifluoromethyl group enhances the biological activity of compounds, making it valuable in medicinal chemistry for developing new drugs with improved efficacy.
  • Material Science: This boronic acid derivative can be employed in the design of advanced materials, such as polymers and coatings, that require specific chemical properties.
  • Analytical Chemistry: It is used in the development of sensors and probes due to its ability to form stable complexes with various analytes, enhancing detection methods in environmental and biological samples.

Citations