🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
46472
CAS Number:
36967-85-8
Trifluorometanosulfonato de benzoilo
Purity:
≥ 98% (Ensayo por titulación)
Synonym(s):
Éster benzoílico del ácido trifluorometanosulfónico, Riflato de benzoilo
Temperature Sensitive
Documents
$287.00 /5G
Tamaño
Request Bulk Quote
Product Information

Benzoyl trifluoromethanesulfonate is a versatile reagent widely utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound serves as an effective electrophilic acylating agent, facilitating the introduction of benzoyl groups into various substrates. Its unique trifluoromethylsulfonyl moiety enhances reactivity, making it a valuable tool for chemists aiming to create complex molecular architectures. Researchers appreciate its ability to streamline synthetic pathways, thereby improving yields and reducing the need for multiple reaction steps.

In addition to its applications in synthetic organic chemistry, Benzoyl trifluoromethanesulfonate is also recognized for its role in the preparation of fluorinated compounds, which are increasingly important in medicinal chemistry and materials science. Its stability and ease of handling further contribute to its appeal in laboratory settings. By incorporating this compound into your research or production processes, you can enhance efficiency and expand the scope of your chemical transformations.

Synonyms
Éster benzoílico del ácido trifluorometanosulfónico, Riflato de benzoilo
CAS Number
36967-85-8
Purity
≥ 98% (Ensayo por titulación)
Molecular Formula
C8H5F3O4S
Molecular Weight
254.18
MDL Number
MFCD17013536
PubChem ID
11064956
Appearance
Líquido transparente entre incoloro y naranja claro y amarillo.
Boiling Point
94 °C/2,2 mmHg
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
Éster benzoílico del ácido trifluorometanosulfónico, Riflato de benzoilo
CAS Number
36967-85-8
Purity
≥ 98% (Ensayo por titulación)
Molecular Formula
C8H5F3O4S
Molecular Weight
254.18
MDL Number
MFCD17013536
PubChem ID
11064956
Appearance
Líquido transparente entre incoloro y naranja claro y amarillo.
Boiling Point
94 °C/2,2 mmHg
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Benzoyl trifluoromethanesulfonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as an effective reagent in the synthesis of various organic molecules, particularly in the formation of esters and amides, enhancing reaction efficiency.
  • Pharmaceutical Development: It plays a crucial role in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs), offering improved yields and purity in drug formulations.
  • Polymer Chemistry: Used as a coupling agent, it aids in the production of specialty polymers, contributing to enhanced material properties such as durability and thermal stability.
  • Fluorination Reactions: This chemical is valuable in introducing trifluoromethyl groups into organic compounds, which can significantly alter their biological activity and chemical properties, making it essential in agrochemical research.
  • Analytical Chemistry: It is employed in various analytical techniques, including chromatography, to improve the separation and detection of complex mixtures, thus benefiting quality control processes in manufacturing.

Citas