2-Nitronaphthalen-1-yl trifluoromethanesulfonate

98%

Reagent Code: #220207
fingerprint
CAS Number 253270-06-3

science Other reagents with same CAS 253270-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.23 g/mol
Formula C₁₁H₆F₃NO₅S
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds. It serves as an electrophilic naphthalene derivative, enabling the introduction of naphthyl groups into complex molecules. Commonly applied in the development of pharmaceuticals, agrochemicals, and functional materials due to its reactivity in transformations such as Suzuki and Heck couplings. Its triflate group enhances leaving group ability, making it highly effective in catalytic reactions. Also utilized in the preparation of fluorescent dyes and optoelectronic materials owing to the aromatic naphthalene backbone.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,380.00
inventory 250mg
10-20 days ฿4,030.00
inventory 1g
10-20 days ฿10,870.00
2-Nitronaphthalen-1-yl trifluoromethanesulfonate
No image available

Used as an intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds. It serves as an electrophilic naphthalene derivative, enabling the introduction of naphthyl groups into complex molecules. Commonly applied in the development of pharmaceuticals, agrochemicals, and functional materials due to its reactivity in transformations such as Suzuki and Heck couplings. Its triflate group enhances leaving group ability, making it highly effective

Used as an intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds. It serves as an electrophilic naphthalene derivative, enabling the introduction of naphthyl groups into complex molecules. Commonly applied in the development of pharmaceuticals, agrochemicals, and functional materials due to its reactivity in transformations such as Suzuki and Heck couplings. Its triflate group enhances leaving group ability, making it highly effective in catalytic reactions. Also utilized in the preparation of fluorescent dyes and optoelectronic materials owing to the aromatic naphthalene backbone.

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...