Ethyl 2,6-dioxocyclohexane-1-carboxylate

95%

Reagent Code: #180628
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CAS Number 195968-41-3

science Other reagents with same CAS 195968-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.18 g/mol
Formula C₉H₁₂O₄
thermostat Physical Properties
Boiling Point 310.9±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.199±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of barbiturate derivatives which act as central nervous system depressants. It serves as a building block in organic synthesis due to its reactive carbonyl and ester functional groups, enabling cyclization and condensation reactions. Commonly employed in the preparation of heterocyclic compounds and fine chemicals where controlled ring structures are required. Its stability and reactivity profile make it suitable for use in both academic research and industrial-scale drug development processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,340.00
inventory 250mg
10-20 days ฿10,760.00
inventory 1g
10-20 days ฿29,030.00

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Ethyl 2,6-dioxocyclohexane-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of barbiturate derivatives which act as central nervous system depressants. It serves as a building block in organic synthesis due to its reactive carbonyl and ester functional groups, enabling cyclization and condensation reactions. Commonly employed in the preparation of heterocyclic compounds and fine chemicals where controlled ring structures are required. Its stability and reactivity profile make it suitab

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of barbiturate derivatives which act as central nervous system depressants. It serves as a building block in organic synthesis due to its reactive carbonyl and ester functional groups, enabling cyclization and condensation reactions. Commonly employed in the preparation of heterocyclic compounds and fine chemicals where controlled ring structures are required. Its stability and reactivity profile make it suitable for use in both academic research and industrial-scale drug development processes.

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