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Catalog Number:
39976
CAS Number:
69807-91-6
2-[3,5-Bis(trifluorométhyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacolique de l'acide 3,5-bis(trifluorométhyl)phénylboronique, 1,3-Bis(trifluorométhyl)-5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène
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Product Information

2-[3,5-Bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a specialized boron compound known for its unique properties and versatility in various applications. This compound features a robust dioxaborolane structure that enhances its stability and reactivity, making it particularly valuable in organic synthesis and materials science. Its trifluoromethyl groups contribute to its lipophilicity, allowing for effective incorporation into complex molecular architectures, which is essential in the development of pharmaceuticals and agrochemicals.

Researchers and industry professionals utilize this compound for its role as a reagent in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Its ability to facilitate the synthesis of complex organic molecules positions it as a crucial tool in drug discovery and development. Additionally, its unique electronic properties make it an attractive candidate for applications in electronic materials and sensors. With its combination of stability, reactivity, and functional versatility, this compound stands out as a valuable asset for advancing research and innovation in various fields.

Synonyms
Ester pinacolique de l'acide 3,5-bis(trifluorométhyl)phénylboronique, 1,3-Bis(trifluorométhyl)-5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène
CAS Number
69807-91-6
Purity
≥ 98% (CG)
Molecular Formula
C14H15BF6O2
Molecular Weight
340.07
MDL Number
MFCD12405516
PubChem ID
9798005
Melting Point
65 - 69 ?C
Appearance
Poudre blanche à blanc cassé en grumeaux
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacolique de l'acide 3,5-bis(trifluorométhyl)phénylboronique, 1,3-Bis(trifluorométhyl)-5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène
CAS Number
69807-91-6
Purity
≥ 98% (CG)
Molecular Formula
C14H15BF6O2
Molecular Weight
340.07
MDL Number
MFCD12405516
PubChem ID
9798005
Melting Point
65 - 69 ?C
Appearance
Poudre blanche à blanc cassé en grumeaux
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-[3,5-Bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly in the formation of carbon-boron bonds, which are crucial for synthesizing complex organic molecules.
  • Pharmaceutical Development: It plays a significant role in drug discovery, where it can be used to create boron-containing compounds that may exhibit unique biological activities, enhancing the efficacy of new medications.
  • Material Science: The chemical is applied in developing advanced materials, particularly in creating polymers with enhanced properties, such as increased thermal stability and chemical resistance.
  • Fluorinated Compounds: Its trifluoromethyl groups contribute to the synthesis of fluorinated compounds, which are important in agrochemicals and pharmaceuticals for improving bioactivity and stability.
  • Analytical Chemistry: This compound can be utilized in analytical methods, such as chromatography, to separate and identify various organic compounds, aiding researchers in quality control and substance identification.

Citations