Diethyl 3-(benzyloxy)cyclobutane-1,1-dicarboxylate

95%

Reagent Code: #177518
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CAS Number 54166-15-3

science Other reagents with same CAS 54166-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.35 g/mol
Formula C₁₇H₂₂O₅
badge Registry Numbers
MDL Number MFCD07700259
thermostat Physical Properties
Boiling Point 368.3 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.0983 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals. Its functionalized cyclobutane core allows for ring-based structural diversification, making it valuable in constructing constrained analogs for drug discovery. The presence of ester groups enables further transformations such as hydrolysis, reduction, or amidation, while the benzyloxy group acts as a protecting group that can be selectively removed under mild conditions. It is often employed in the synthesis of bioactive molecules where cyclobutane rings are used to modulate metabolic stability, conformation, and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 250mg
10-20 days ฿4,000.00
inventory 1g
10-20 days ฿9,600.00
inventory 5g
10-20 days ฿28,800.00
inventory 25g
10-20 days ฿96,000.00

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Diethyl 3-(benzyloxy)cyclobutane-1,1-dicarboxylate
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Used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals. Its functionalized cyclobutane core allows for ring-based structural diversification, making it valuable in constructing constrained analogs for drug discovery. The presence of ester groups enables further transformations such as hydrolysis, reduction, or amidation, while the benzyloxy group acts as a protecting group that can be selectively removed under mild conditions. It is often employed in the synth

Used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals. Its functionalized cyclobutane core allows for ring-based structural diversification, making it valuable in constructing constrained analogs for drug discovery. The presence of ester groups enables further transformations such as hydrolysis, reduction, or amidation, while the benzyloxy group acts as a protecting group that can be selectively removed under mild conditions. It is often employed in the synthesis of bioactive molecules where cyclobutane rings are used to modulate metabolic stability, conformation, and binding affinity.

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