(R)-(-)-N-(2,3-Epoxypropyl)phthalimide

≥98.0% (GC)

Reagent Code: #229992
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CAS Number 181140-34-1

science Other reagents with same CAS 181140-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₁₁H₉NO₃
badge Registry Numbers
MDL Number MFCD04973349
thermostat Physical Properties
Melting Point 100-102°C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its epoxide ring allows for regioselective and stereospecific ring-opening reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of beta-amino alcohols and chiral intermediates for drugs, including protease inhibitors and antiviral agents. Also utilized in the development of enantiomerically pure epichlorohydrin derivatives. Its phthalimide group acts as a protected amine, enabling stepwise construction of complex molecules in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿330.00
5g
10-20 days ฿880.00
100g
10-20 days ฿14,880.00
25g
10-20 days ฿4,020.00
(R)-(-)-N-(2,3-Epoxypropyl)phthalimide
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its epoxide ring allows for regioselective and stereospecific ring-opening reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of beta-amino alcohols and chiral intermediates for drugs, including protease inhibitors and antiviral agents. Also utilized in the development of enantiomerically pure epichlorohydrin derivatives. Its phthalimide group acts as a protected

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its epoxide ring allows for regioselective and stereospecific ring-opening reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of beta-amino alcohols and chiral intermediates for drugs, including protease inhibitors and antiviral agents. Also utilized in the development of enantiomerically pure epichlorohydrin derivatives. Its phthalimide group acts as a protected amine, enabling stepwise construction of complex molecules in medicinal chemistry.

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