Methyl 3,3-dimethoxycyclobutanecarboxylate

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Reagent Code: #210354
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CAS Number 98231-07-3

science Other reagents with same CAS 98231-07-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.19 g/mol
Formula C₈H₁₄O₄
badge Registry Numbers
MDL Number MFCD11111944
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of cyclobutane-based compounds for pharmaceuticals and agrochemicals. Its masked ketone functionality, protected as a dimethyl ketal, allows selective deprotection under mild acidic conditions to generate reactive ketone intermediates. This makes it valuable in multi-step syntheses where functional group compatibility is crucial. It is also employed in the development of bioactive molecules, including drug candidates requiring strained ring systems for conformational restriction.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿800.00
inventory 10g
10-20 days ฿1,280.00
inventory 25g
10-20 days ฿2,520.00
inventory 100g
10-20 days ฿8,920.00

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Methyl 3,3-dimethoxycyclobutanecarboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of cyclobutane-based compounds for pharmaceuticals and agrochemicals. Its masked ketone functionality, protected as a dimethyl ketal, allows selective deprotection under mild acidic conditions to generate reactive ketone intermediates. This makes it valuable in multi-step syntheses where functional group compatibility is crucial. It is also employed in the development of bioactive molecules, including drug candidates requiri

Used as a key intermediate in organic synthesis, particularly in the preparation of cyclobutane-based compounds for pharmaceuticals and agrochemicals. Its masked ketone functionality, protected as a dimethyl ketal, allows selective deprotection under mild acidic conditions to generate reactive ketone intermediates. This makes it valuable in multi-step syntheses where functional group compatibility is crucial. It is also employed in the development of bioactive molecules, including drug candidates requiring strained ring systems for conformational restriction.

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