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Catalog Number:
23334
CAS Number:
204981-49-7
Ácido 2,2-dimetilpropil-4'-(trifluorometil)benzoato-2'-borónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 2-(neopentiloxicarbonil)-5-(trifluorometil)fenilborónico
Documents
$168.35 /100 mg
Tamaño
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Product Information

2,2-Dimethylpropyl-4'-(trifluoromethyl)benzoate-2'-boronic acid is a versatile compound that plays a significant role 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 development of complex organic molecules. Its unique trifluoromethyl group enhances its reactivity and selectivity, allowing researchers to create compounds with tailored properties for pharmaceuticals and agrochemicals.

In addition to its synthetic applications, this compound is also utilized in the development of sensors and materials due to its boronic acid functionality, which can form reversible covalent bonds with diols. This property is particularly beneficial in the design of glucose sensors for diabetes management, showcasing its potential in healthcare applications. With its distinctive features and practical uses, 2,2-Dimethylpropyl-4'-(trifluoromethyl)benzoate-2'-boronic acid stands out as a valuable asset for researchers and industry professionals seeking innovative solutions in chemical synthesis and material science.

Synonyms
Ácido 2-(neopentiloxicarbonil)-5-(trifluorometil)fenilborónico
CAS Number
204981-49-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H16BF3O4
Molecular Weight
304.07
MDL Number
MFCD01631850
PubChem ID
15462268
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 2-(neopentiloxicarbonil)-5-(trifluorometil)fenilborónico
CAS Number
204981-49-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H16BF3O4
Molecular Weight
304.07
MDL Number
MFCD01631850
PubChem ID
15462268
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,2-Dimethylpropyl-4'-(trifluoromethyl)benzoate-2'-boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the synthesis of complex molecules through cross-coupling reactions, which are essential in developing pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a crucial role in drug discovery, particularly in the design of boronic acid-based inhibitors that target specific enzymes, offering potential treatments for various diseases, including cancer.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, enhancing properties such as thermal stability and chemical resistance, which are vital in industrial applications.
  • Analytical Chemistry: It is employed in the preparation of sensors and probes for detecting biomolecules, providing a reliable method for monitoring environmental pollutants or biological markers in clinical diagnostics.
  • Bioconjugation: This chemical is valuable in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems and improving therapeutic efficacy.

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