(3S,7aR)-3-(Trichloromethyl)tetrahydro-1H,3H-pyrrolo[1,2-c]oxazol-1-one

98%

Reagent Code: #233292
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CAS Number 1330286-50-4

science Other reagents with same CAS 1330286-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.5 g/mol
Formula C₇H₈Cl₃NO₂
badge Registry Numbers
MDL Number MFCD08274465
thermostat Physical Properties
Boiling Point 338.6±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.59±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its rigid polycyclic structure and trichloromethyl group make it valuable in asymmetric synthesis, helping to control stereoselectivity during carbon–carbon bond formation. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic peptide transition states. Also utilized in agrochemical research for designing enantioselective catalysts and enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,350.00
inventory 1g
10-20 days ฿19,600.00

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(3S,7aR)-3-(Trichloromethyl)tetrahydro-1H,3H-pyrrolo[1,2-c]oxazol-1-one
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its rigid polycyclic structure and trichloromethyl group make it valuable in asymmetric synthesis, helping to control stereoselectivity during carbon–carbon bond formation. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic peptide transition states. Also utilized in agrochemical research for

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its rigid polycyclic structure and trichloromethyl group make it valuable in asymmetric synthesis, helping to control stereoselectivity during carbon–carbon bond formation. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic peptide transition states. Also utilized in agrochemical research for designing enantioselective catalysts and enzyme inhibitors.

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