2-Oxo-2H-chromen-7-yl Trifluoromethanesulfonate

≥98%

Reagent Code: #221603
fingerprint
CAS Number 108530-10-5

science Other reagents with same CAS 108530-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.2 g/mol
Formula C₁₀H₅F₃O₅S
badge Registry Numbers
MDL Number MFCD18382236
thermostat Physical Properties
Melting Point 81-85°C
inventory_2 Storage & Handling
Storage Room temperature

description 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,720.00
1g
10-20 days ฿5,990.00
5g
10-20 days ฿29,390.00
2-Oxo-2H-chromen-7-yl Trifluoromethanesulfonate
No image available

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 pro

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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...