(S)-2-(Benzyloxy)-1-(pyrrolidin-1-yl)propan-1-one

95%

Reagent Code: #236026
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CAS Number 122151-32-0

science Other reagents with same CAS 122151-32-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.31 g/mol
Formula C₁₄H₁₉NO₂
badge Registry Numbers
MDL Number MFCD16618590
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to the presence of the pyrrolidine ring and chiral center. Also utilized in medicinal chemistry for building complex molecules through nucleophilic addition or reduction reactions, where the benzyl group acts as a protecting group that can be easily removed under mild conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,960.00
inventory 250mg
10-20 days ฿4,370.00
inventory 1g
10-20 days ฿15,190.00
inventory 5g
10-20 days ฿38,500.00

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(S)-2-(Benzyloxy)-1-(pyrrolidin-1-yl)propan-1-one
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to the presence of the pyrrolidine ring and chiral center. Also utilized in medicinal chemistry for buil

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to the presence of the pyrrolidine ring and chiral center. Also utilized in medicinal chemistry for building complex molecules through nucleophilic addition or reduction reactions, where the benzyl group acts as a protecting group that can be easily removed under mild conditions.

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