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

97%

Reagent Code: #233343
fingerprint
CAS Number 104010-72-2

science Other reagents with same CAS 104010-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.16 g/mol
Formula C₈H₁₀O₃
badge Registry Numbers
MDL Number MFCD08166478
thermostat Physical Properties
Melting Point 68.1-69.4 °C
Boiling Point 50 °C at 0.05 mmHg
inventory_2 Storage & Handling
Density 1.156±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of antiviral and antitumor agents, particularly in the preparation of nucleoside analogs. Its rigid cyclic structure helps mimic sugar moieties in nucleosides, enhancing stability and biological activity. Commonly employed in medicinal chemistry for modifying nucleic acid components to improve resistance to enzymatic degradation. Also utilized in the development of prodrugs and in asymmetric synthesis due to its chiral backbone.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,220.00
inventory 250mg
10-20 days ฿1,840.00
inventory 1g
10-20 days ฿4,720.00
inventory 10g
10-20 days ฿30,420.00
inventory 25g
10-20 days ฿66,530.00
inventory 5g
10-20 days ฿19,010.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3aS,6aS)-2,2-Dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one
No image available

Used as a key intermediate in the synthesis of antiviral and antitumor agents, particularly in the preparation of nucleoside analogs. Its rigid cyclic structure helps mimic sugar moieties in nucleosides, enhancing stability and biological activity. Commonly employed in medicinal chemistry for modifying nucleic acid components to improve resistance to enzymatic degradation. Also utilized in the development of prodrugs and in asymmetric synthesis due to its chiral backbone.

Used as a key intermediate in the synthesis of antiviral and antitumor agents, particularly in the preparation of nucleoside analogs. Its rigid cyclic structure helps mimic sugar moieties in nucleosides, enhancing stability and biological activity. Commonly employed in medicinal chemistry for modifying nucleic acid components to improve resistance to enzymatic degradation. Also utilized in the development of prodrugs and in asymmetric synthesis due to its chiral backbone.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...