Methyl 4,4-dimethyl-2,6-dioxocyclohexane-1-carboxylate

95%

Reagent Code: #203366
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CAS Number 54334-96-2

science Other reagents with same CAS 54334-96-2

blur_circular Chemical Specifications

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Weight 198.22 g/mol
Formula C₁₀H₁₄O₄
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MDL Number MFCD31588691
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of steroids and steroidal analogs. Its structure supports ring-functionalization reactions, making it valuable in pharmaceutical research for developing hormone-based therapeutics. Commonly employed in the synthesis of modified cyclohexanone derivatives used in anti-inflammatory and metabolic disorder studies. Also utilized in the construction of polycyclic frameworks via aldol condensation or alkylation reactions under controlled conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,610.00
inventory 1g
10-20 days ฿60,500.00
inventory 250mg
10-20 days ฿20,880.00

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Methyl 4,4-dimethyl-2,6-dioxocyclohexane-1-carboxylate
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Used as an intermediate in organic synthesis, particularly in the preparation of steroids and steroidal analogs. Its structure supports ring-functionalization reactions, making it valuable in pharmaceutical research for developing hormone-based therapeutics. Commonly employed in the synthesis of modified cyclohexanone derivatives used in anti-inflammatory and metabolic disorder studies. Also utilized in the construction of polycyclic frameworks via aldol condensation or alkylation reactions under control

Used as an intermediate in organic synthesis, particularly in the preparation of steroids and steroidal analogs. Its structure supports ring-functionalization reactions, making it valuable in pharmaceutical research for developing hormone-based therapeutics. Commonly employed in the synthesis of modified cyclohexanone derivatives used in anti-inflammatory and metabolic disorder studies. Also utilized in the construction of polycyclic frameworks via aldol condensation or alkylation reactions under controlled conditions.

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