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Catalog Number:
23392
CAS Number:
163295-75-8
Chlorure de 4-trifluorométhylbenzylsulfonyle
Purity:
≥ 95%
Synonym(s):
Chlorure de ([4-(trifluorométhyl)phényl]méthyl)sulfonyle, Chlorure de [4-(trifluorométhyl)phényl]méthanesulfonyle, Chlorure de 4-trifluorométhyl-α-toluènesulfonyle
Hazmat
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Product Information

4-Trifluoromethylbenzylsulfonyl chloride is a versatile sulfonyl chloride compound known for its unique trifluoromethyl group, which enhances its reactivity and solubility in various organic solvents. This compound is particularly valuable in the synthesis of pharmaceuticals and agrochemicals, where it serves as a key intermediate in the development of sulfonamide derivatives. Its ability to introduce a trifluoromethyl group into organic molecules makes it an essential reagent for researchers aiming to enhance the biological activity of their compounds.

In addition to its applications in medicinal chemistry, 4-Trifluoromethylbenzylsulfonyl chloride is also utilized in the production of specialty chemicals and materials, offering advantages such as improved thermal stability and increased lipophilicity in the final products. Its unique properties make it an attractive choice for professionals looking to innovate in drug design or develop new agrochemical formulations. With its proven track record in enhancing compound efficacy, this sulfonyl chloride is a valuable addition to any research or industrial laboratory.

Synonyms
Chlorure de ([4-(trifluorométhyl)phényl]méthyl)sulfonyle, Chlorure de [4-(trifluorométhyl)phényl]méthanesulfonyle, Chlorure de 4-trifluorométhyl-α-toluènesulfonyle
CAS Number
163295-75-8
Purity
≥ 95%
Molecular Formula
C8H6ClF3O2S
Molecular Weight
258.65
MDL Number
MFCD01631932
PubChem ID
594332
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8°C
Warnings
Corrosif! Irritant!
General Information
Synonyms
Chlorure de ([4-(trifluorométhyl)phényl]méthyl)sulfonyle, Chlorure de [4-(trifluorométhyl)phényl]méthanesulfonyle, Chlorure de 4-trifluorométhyl-α-toluènesulfonyle
CAS Number
163295-75-8
Purity
≥ 95%
Molecular Formula
C8H6ClF3O2S
Molecular Weight
258.65
MDL Number
MFCD01631932
PubChem ID
594332
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8°C
Warnings
Corrosif! Irritant!
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
Corrosif! Irritant!
Applications

4-Trifluoromethylbenzylsulfonyl chloride is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as an essential reagent in the synthesis of various sulfonyl-containing compounds, enabling the development of new pharmaceuticals and agrochemicals.
  • Drug Development: Its unique trifluoromethyl group enhances the biological activity of drug candidates, making it valuable in the pharmaceutical industry for creating more effective medications.
  • Material Science: Used in the modification of polymers, it improves the thermal and chemical resistance of materials, which is crucial for applications in coatings and adhesives.
  • Bioconjugation: This compound is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, aiding in the development of targeted drug delivery systems.
  • Analytical Chemistry: It acts as a derivatizing agent in analytical methods, enhancing the detection and quantification of various compounds in complex mixtures.

Citations