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Catalog Number:
23386
CAS Number:
127162-96-3
Chlorure de 3-trifluorométhylbenzylsulfonyle
Purity:
≥ 96% (RMN)
Synonym(s):
Chlorure de [3-(trifluorométhyl)phényl]méthanesulfonyle
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$67.60 /250 mg
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Product Information

3-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 widely utilized in the synthesis of pharmaceuticals and agrochemicals, serving as a key intermediate in the development of biologically active molecules. Its ability to introduce a sulfonyl chloride functional group makes it particularly valuable in the formation of sulfonamides and other derivatives, which are crucial in medicinal chemistry.

Researchers and industry professionals appreciate 3-Trifluoromethylbenzylsulfonyl chloride for its efficiency in facilitating nucleophilic substitutions, allowing for the rapid construction of complex molecular architectures. Its distinctive properties enable the development of compounds with enhanced biological activity and selectivity, making it an essential tool in drug discovery and development. Additionally, its stability under various conditions ensures reliable performance in laboratory and industrial applications, providing a significant advantage over similar compounds.

Synonyms
Chlorure de [3-(trifluorométhyl)phényl]méthanesulfonyle
CAS Number
127162-96-3
Purity
≥ 96% (RMN)
Molecular Formula
C8H6ClF3O2S
Molecular Weight
258.65
MDL Number
MFCD01631926
PubChem ID
2794646
Melting Point
54-62 ºC
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
Chlorure de [3-(trifluorométhyl)phényl]méthanesulfonyle
CAS Number
127162-96-3
Purity
≥ 96% (RMN)
Molecular Formula
C8H6ClF3O2S
Molecular Weight
258.65
MDL Number
MFCD01631926
PubChem ID
2794646
Melting Point
54-62 ºC
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in creating sulfonamide drugs that exhibit antimicrobial properties.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and fungicides, enhancing their effectiveness due to the trifluoromethyl group that improves bioactivity.
  • Material Science: The compound plays a role in developing specialty polymers and coatings, providing enhanced chemical resistance and durability in various industrial applications.
  • Organic Synthesis: It is a valuable reagent in organic chemistry for introducing sulfonyl groups into molecules, facilitating the creation of complex organic compounds with diverse functionalities.
  • Research Laboratories: This chemical is frequently employed in laboratories for the synthesis of novel compounds, allowing researchers to explore new chemical properties and reactions.

Citations