8-(Trifluoromethyl)naphthalen-1-ol

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Reagent Code: #131791
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CAS Number 33533-47-0

science Other reagents with same CAS 33533-47-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.17 g/mol
Formula C₁₁H₇F₃O
badge Registry Numbers
MDL Number MFCD09266206
thermostat Physical Properties
Melting Point 94-96 °C(Solv: pentane (109-66-0))
Boiling Point 299.1±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.364±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its fluorinated aromatic structure, which can enhance metabolic stability and bioavailability in active compounds. Its naphtholic core allows for easy functionalization, making it valuable in the development of specialty chemicals, including liquid crystal materials and fluorescent dyes. The electron-withdrawing trifluoromethyl group influences the compound’s reactivity and binding properties, useful in medicinal chemistry for designing enzyme inhibitors or receptor ligands.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,130.00
inventory 250mg
10-20 days ฿13,830.00
inventory 1g
10-20 days ฿37,330.00

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8-(Trifluoromethyl)naphthalen-1-ol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its fluorinated aromatic structure, which can enhance metabolic stability and bioavailability in active compounds. Its naphtholic core allows for easy functionalization, making it valuable in the development of specialty chemicals, including liquid crystal materials and fluorescent dyes. The electron-withdrawing trifluoromethyl group influences the compound’s reactivity and binding properties, useful in medicinal chemist

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its fluorinated aromatic structure, which can enhance metabolic stability and bioavailability in active compounds. Its naphtholic core allows for easy functionalization, making it valuable in the development of specialty chemicals, including liquid crystal materials and fluorescent dyes. The electron-withdrawing trifluoromethyl group influences the compound’s reactivity and binding properties, useful in medicinal chemistry for designing enzyme inhibitors or receptor ligands.

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