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Catalog Number:
46461
CAS Number:
129112-26-1
2-Iodophenyl trifluoromethanesulfonate
Purity:
≥ 98% (GC)
Synonym(s):
Trifluoromethanesulfonic acid 2-iodophenyl ester, 2-Iodophenyl triflate
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Product Information

2-Iodophenyl trifluoromethanesulfonate is a versatile chemical compound widely recognized for its utility in organic synthesis and medicinal chemistry. This compound serves as an effective electrophilic reagent, facilitating the introduction of the 2-iodophenyl group into various substrates. Its trifluoromethanesulfonate moiety enhances reactivity, making it particularly valuable in nucleophilic substitution reactions. Researchers and industry professionals utilize 2-Iodophenyl trifluoromethanesulfonate in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount. Its unique properties allow for the creation of complex molecular architectures, streamlining the synthesis of target compounds.

The compound's ability to act as a leaving group in reactions further underscores its significance in synthetic pathways, providing a strategic advantage over similar reagents. With its high reactivity and selectivity, 2-Iodophenyl trifluoromethanesulfonate is an essential tool for chemists aiming to innovate and optimize their synthetic processes, ultimately leading to more effective and efficient product development.

Synonyms
Trifluoromethanesulfonic acid 2-iodophenyl ester, 2-Iodophenyl triflate
CAS Number
129112-26-1
Purity
≥ 98% (GC)
Molecular Formula
C7H4F3IO3S
Molecular Weight
352.07
MDL Number
MFCD07784326
PubChem ID
10784152
Density
1.94
Appearance
Light orange to yellow to green clear liquid
Refractive Index
n20D 1.51
Conditions
Store at RT
General Information
Synonyms
Trifluoromethanesulfonic acid 2-iodophenyl ester, 2-Iodophenyl triflate
CAS Number
129112-26-1
Purity
≥ 98% (GC)
Molecular Formula
C7H4F3IO3S
Molecular Weight
352.07
MDL Number
MFCD07784326
PubChem ID
10784152
Density
1.94
Appearance
Light orange to yellow to green clear liquid
Refractive Index
n20D 1.51
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-Iodophenyl trifluoromethanesulfonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Pharmaceutical Development: It is used in the development of new pharmaceuticals, particularly in the modification of drug candidates to enhance their efficacy and selectivity.
  • Material Science: The compound is applied in the creation of advanced materials, including polymers and coatings, which benefit from its unique chemical properties.
  • Bioconjugation: It plays a crucial role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Research in Chemical Biology: The compound is valuable in chemical biology for studying protein interactions and cellular processes, providing insights that can lead to innovative treatments.

Citations