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Catalog Number:
10626
CAS Number:
93128-04-2
4-Bromophenacyl-trifluoromethanesulfonate
Synonym(s):
4-Bromophenacyl-trifluoromesylate, 4-Bromophenacyl triflate
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$106.96 /25MG
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Product Information

4-Bromophenacyl-trifluoromethanesulfonate is a versatile chemical compound widely utilized in organic synthesis and medicinal chemistry. This compound serves as an effective electrophilic reagent, particularly in the development of pharmaceuticals and agrochemicals. Its unique trifluoromethanesulfonate group enhances its reactivity, making it an excellent choice for various substitution reactions. Researchers often leverage its properties to create complex molecular structures, facilitating the synthesis of biologically active compounds.

In addition to its synthetic applications, 4-Bromophenacyl-trifluoromethanesulfonate is recognized for its role in the study of enzyme mechanisms and protein interactions. Its ability to selectively modify functional groups allows for the exploration of biochemical pathways, making it invaluable in both academic and industrial research settings. With its robust reactivity and broad applicability, this compound stands out as a key tool for chemists aiming to innovate and expand their research horizons.

Synonyms
4-Bromophenacyl-trifluoromesylate, 4-Bromophenacyl triflate
CAS Number
93128-04-2
Molecular Formula
C9H6BrF3O4S
Molecular Weight
347.11
MDL Number
MFCD00467440
PubChem ID
125008
Conditions
Store at 0-8°C
General Information
Synonyms
4-Bromophenacyl-trifluoromesylate, 4-Bromophenacyl triflate
CAS Number
93128-04-2
Molecular Formula
C9H6BrF3O4S
Molecular Weight
347.11
MDL Number
MFCD00467440
PubChem ID
125008
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Bromophenacyl-trifluoromethanesulfonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic molecules, particularly in creating complex structures that are essential in pharmaceuticals.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Fluorination Reactions: The trifluoromethanesulfonate group facilitates selective fluorination, which is crucial in developing fluorinated compounds that exhibit unique properties in medicinal chemistry.
  • Analytical Chemistry: This chemical is used in analytical methods for detecting and quantifying specific biomolecules, aiding in quality control processes in the pharmaceutical industry.
  • Material Science: It finds applications in the development of advanced materials, particularly in creating polymers with enhanced thermal and chemical stability.

Citations