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Catalog Number:
40247
CAS Number:
871332-97-7
3-Methoxy-5-(trifluoromethyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Methoxy-5-(trifluoromethyl)benzeneboronic acid
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Product Information

3-Methoxy-5-(trifluoromethyl)phenylboronic acid is a versatile boronic acid derivative known for its unique trifluoromethyl group, which enhances its reactivity and selectivity in various chemical reactions. This compound is particularly valuable in the field of organic synthesis, where it serves as a crucial building block for the development of pharmaceuticals and agrochemicals. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it an essential reagent for creating complex molecular architectures, allowing researchers to efficiently construct carbon-carbon bonds.

Additionally, 3-Methoxy-5-(trifluoromethyl)phenylboronic acid exhibits excellent solubility in organic solvents, facilitating its use in diverse reaction conditions. Its distinctive properties make it a preferred choice for chemists looking to optimize reaction yields and improve the efficiency of synthetic pathways. This compound is also being explored for applications in materials science, particularly in the development of functionalized polymers and advanced materials. With its broad range of applications, this boronic acid derivative stands out as a valuable tool for researchers and industry professionals alike.

Synonyms
3-Methoxy-5-(trifluoromethyl)benzeneboronic acid
CAS Number
871332-97-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BF3O3
Molecular Weight
219.95
MDL Number
MFCD08056362
PubChem ID
44717590
Melting Point
162 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Methoxy-5-(trifluoromethyl)benzeneboronic acid
CAS Number
871332-97-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BF3O3
Molecular Weight
219.95
MDL Number
MFCD08056362
PubChem ID
44717590
Melting Point
162 °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-Methoxy-5-(trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, enhancing the efficiency of chemical reactions.
  • Medicinal Chemistry: It plays a crucial role in the design of novel drug candidates, especially in targeting specific biological pathways, which can lead to more effective treatments with fewer side effects.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and coatings, that exhibit improved thermal and chemical stability, making them suitable for demanding applications.
  • Bioconjugation: It is utilized in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is essential in the development of biosensors and targeted drug delivery systems.
  • Environmental Chemistry: This chemical aids in the detection and removal of pollutants, contributing to environmental monitoring and remediation efforts, thereby supporting sustainability initiatives.

Citations