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Catalog Number:
39959
CAS Number:
1073339-21-5
2-[2-(Trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(trifluoromethyl)benzene
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Product Information

2-[2-(Trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a specialized boron-containing compound known for its unique properties and versatility in various applications. This compound features a trifluoromethyl group, enhancing its reactivity and making it particularly valuable in organic synthesis and materials science. Its structure allows for effective coordination with various substrates, making it an excellent choice for researchers focusing on catalysis and the development of new chemical processes.

In the pharmaceutical industry, this compound can be utilized in the synthesis of complex molecules, providing a pathway for the creation of innovative drugs. Additionally, its properties lend themselves well to applications in agrochemicals, where it can be used to develop more effective pesticides and herbicides. The stability and reactivity of 2-[2-(Trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane make it a valuable tool for chemists looking to enhance their research and development efforts.

Synonyms
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(trifluoromethyl)benzene
CAS Number
1073339-21-5
Purity
≥ 98% (GC)
Molecular Formula
C13H16BF3O2
Molecular Weight
272.07
MDL Number
MFCD06795676
PubChem ID
17750282
Density
1.15 g/mL
Appearance
Clear colorless liquid
Boiling Point
73 ?C / 2 mmHg (Lit.)
Refractive Index
n20D = 1.45
Conditions
Store at RT
General Information
Synonyms
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(trifluoromethyl)benzene
CAS Number
1073339-21-5
Purity
≥ 98% (GC)
Molecular Formula
C13H16BF3O2
Molecular Weight
272.07
MDL Number
MFCD06795676
PubChem ID
17750282
Density
1.15 g/mL
Appearance
Clear colorless liquid
Boiling Point
73 ?C / 2 mmHg (Lit.)
Refractive Index
n20D = 1.45
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

2-[2-(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 synthesis of complex molecules. Its unique structure allows for selective reactions, making it invaluable for chemists developing new pharmaceuticals.
  • Material Science: In the development of advanced materials, this chemical is used to enhance the properties of polymers and coatings. Its incorporation can improve thermal stability and chemical resistance, which is crucial for industrial applications.
  • Fluorinated Compounds: The trifluoromethyl group in this compound is beneficial for creating fluorinated derivatives, which are important in agrochemicals and pharmaceuticals. These derivatives often exhibit enhanced biological activity and stability.
  • Analytical Chemistry: This chemical is employed as a standard in analytical methods, helping researchers accurately quantify other compounds. Its stability and reactivity profile make it an excellent choice for calibration in various assays.
  • Environmental Chemistry: Researchers use this compound to study the behavior of fluorinated chemicals in the environment. Understanding its interactions helps in assessing the environmental impact of similar compounds, guiding regulatory measures.

Citations