Ethyl 2-(9H-fluoren-9-yl)acetate

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Reagent Code: #183524
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CAS Number 159803-52-8

science Other reagents with same CAS 159803-52-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.31 g/mol
Formula C₁₇H₁₆O₂
badge Registry Numbers
MDL Number MFCD01632142
thermostat Physical Properties
Boiling Point 378.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Ethyl 2-(9H-fluoren-9-yl)acetate serves as a versatile intermediate in organic synthesis, especially for constructing fluorene-based structures applied in pharmaceuticals, agrochemicals, and advanced functional materials. The fluorene core provides inherent fluorescence, rendering it useful in the creation of fluorescent probes, sensors, and conjugated polymers. The ethyl ester group facilitates straightforward modifications, such as hydrolysis to the acid or conversion to amides and alcohols, enhancing its utility in medicinal chemistry and materials science.

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inventory 1g
10-20 days ฿15,990.00

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Ethyl 2-(9H-fluoren-9-yl)acetate
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Ethyl 2-(9H-fluoren-9-yl)acetate serves as a versatile intermediate in organic synthesis, especially for constructing fluorene-based structures applied in pharmaceuticals, agrochemicals, and advanced functional materials. The fluorene core provides inherent fluorescence, rendering it useful in the creation of fluorescent probes, sensors, and conjugated polymers. The ethyl ester group facilitates straightforward modifications, such as hydrolysis to the acid or conversion to amides and alcohols, enhancing

Ethyl 2-(9H-fluoren-9-yl)acetate serves as a versatile intermediate in organic synthesis, especially for constructing fluorene-based structures applied in pharmaceuticals, agrochemicals, and advanced functional materials. The fluorene core provides inherent fluorescence, rendering it useful in the creation of fluorescent probes, sensors, and conjugated polymers. The ethyl ester group facilitates straightforward modifications, such as hydrolysis to the acid or conversion to amides and alcohols, enhancing its utility in medicinal chemistry and materials science.

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