Ethyl 3-oxo-3-(thiophen-2-yl)propanoate

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Reagent Code: #182418
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CAS Number 13669-10-8

science Other reagents with same CAS 13669-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.24 g/mol
Formula C₉H₁₀O₃S
badge Registry Numbers
MDL Number MFCD00542649
thermostat Physical Properties
Boiling Point 291°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of heterocyclic compounds. Its structure allows for easy functionalization, making it valuable in creating biologically active molecules. Commonly employed in condensation reactions to form pyrazoles, isoxazoles, and other nitrogen-containing rings. Also utilized in the development of organic semiconductors due to the presence of the thiophene moiety, which enhances electronic properties in conjugated systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿132.00
inventory 1g
10-20 days ฿154.00
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Ethyl 3-oxo-3-(thiophen-2-yl)propanoate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of heterocyclic compounds. Its structure allows for easy functionalization, making it valuable in creating biologically active molecules. Commonly employed in condensation reactions to form pyrazoles, isoxazoles, and other nitrogen-containing rings. Also utilized in the development of organic semiconductors due to the presence of the thiophene moiety, which enhances electronic properties in conj
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of heterocyclic compounds. Its structure allows for easy functionalization, making it valuable in creating biologically active molecules. Commonly employed in condensation reactions to form pyrazoles, isoxazoles, and other nitrogen-containing rings. Also utilized in the development of organic semiconductors due to the presence of the thiophene moiety, which enhances electronic properties in conjugated systems.
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