(3aR,6aR)-2,2-Dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one

95%

Reagent Code: #230838
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CAS Number 115509-13-2

science Other reagents with same CAS 115509-13-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.16 g/mol
Formula C₈H₁₀O₃
badge Registry Numbers
MDL Number MFCD08166479
thermostat Physical Properties
Boiling Point 243.842 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral building block in the synthesis of antiviral and antitumor agents. Its rigid cyclic structure and stereochemistry make it valuable for constructing complex molecules in pharmaceutical research. Commonly employed in asymmetric synthesis to introduce chirality, especially in nucleoside analogs and natural product derivatives. Also utilized in the development of protease inhibitors due to its ability to mimic transition states in enzymatic reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,280.00
inventory 5g
10-20 days ฿6,080.00
inventory 25g
10-20 days ฿24,000.00
inventory 100g
10-20 days ฿97,460.00
(3aR,6aR)-2,2-Dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one
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Used as a key chiral building block in the synthesis of antiviral and antitumor agents. Its rigid cyclic structure and stereochemistry make it valuable for constructing complex molecules in pharmaceutical research. Commonly employed in asymmetric synthesis to introduce chirality, especially in nucleoside analogs and natural product derivatives. Also utilized in the development of protease inhibitors due to its ability to mimic transition states in enzymatic reactions.

Used as a key chiral building block in the synthesis of antiviral and antitumor agents. Its rigid cyclic structure and stereochemistry make it valuable for constructing complex molecules in pharmaceutical research. Commonly employed in asymmetric synthesis to introduce chirality, especially in nucleoside analogs and natural product derivatives. Also utilized in the development of protease inhibitors due to its ability to mimic transition states in enzymatic reactions.

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