p-Tolyl Trifluoromethanesulfonate
98%
- Product Code: 121844
CAS:
29540-83-8
Molecular Weight: | 240.2 g./mol | Molecular Formula: | C₈H₇F₃O₃S |
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EC Number: | MDL Number: | MFCD00192507 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is commonly employed as a triflating agent to convert alcohols, phenols, and amines into their corresponding triflates, which are highly reactive intermediates in cross-coupling reactions like Suzuki, Heck, and Sonogashira reactions. Additionally, it serves as a catalyst or promoter in various electrophilic aromatic substitution reactions, enabling the introduction of functional groups into aromatic compounds. Its stability and reactivity make it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.
Product Specification:
Test | Specification |
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Appearance | Colorless To Light Yellow Liquid |
Purity (%) | 97.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,270.00 |
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5.000 | 10-20 days | ฿5,650.00 |
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p-Tolyl Trifluoromethanesulfonate
Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is commonly employed as a triflating agent to convert alcohols, phenols, and amines into their corresponding triflates, which are highly reactive intermediates in cross-coupling reactions like Suzuki, Heck, and Sonogashira reactions. Additionally, it serves as a catalyst or promoter in various electrophilic aromatic substitution reactions, enabling the introduction of functional groups into aromatic compounds. Its stability and reactivity make it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.
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