2-Oxo-2H-chromen-7-yl Trifluoromethanesulfonate
≥98%
- Product Code: 221603
CAS:
108530-10-5
Molecular Weight: | 294.2 g./mol | Molecular Formula: | C₁₀H₅F₃O₅S |
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EC Number: | MDL Number: | MFCD18382236 | |
Melting Point: | 81-85°C | Boiling Point: | |
Density: | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its triflate group acts as a strong leaving group, making it highly reactive toward nucleophiles and organometallic reagents. Commonly employed in the preparation of coumarin derivatives, which exhibit biological activities including anticoagulant, antimicrobial, and anticancer properties. Also utilized in materials science for synthesizing fluorescent dyes and optical brighteners due to the inherent photophysical properties of the coumarin scaffold.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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250mg | 10-20 days | ฿1,720.00 |
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1g | 10-20 days | ฿5,990.00 |
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5g | 10-20 days | ฿29,390.00 |
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2-Oxo-2H-chromen-7-yl Trifluoromethanesulfonate
Used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its triflate group acts as a strong leaving group, making it highly reactive toward nucleophiles and organometallic reagents. Commonly employed in the preparation of coumarin derivatives, which exhibit biological activities including anticoagulant, antimicrobial, and anticancer properties. Also utilized in materials science for synthesizing fluorescent dyes and optical brighteners due to the inherent photophysical properties of the coumarin scaffold.
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