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

98%

Reagent Code: #234641
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CAS Number 161596-47-0

science Other reagents with same CAS 161596-47-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₁₁H₉NO₃
badge Registry Numbers
MDL Number MFCD04973350
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in organic synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and bioactive compounds. Its epoxide ring allows for regioselective ring-opening reactions with nucleophiles, enabling the introduction of functionalized side chains in drug molecules. Commonly employed in the synthesis of β-amino alcohols and as an intermediate in the production of protease inhibitors and other therapeutic agents. Also utilized in the development of chiral ligands and catalysts for asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 5g
10-20 days ฿168.00
inventory 100g
10-20 days ฿2,170.00
inventory 500g
10-20 days ฿10,500.00
inventory 25g
10-20 days ฿550.00
(S)-()-N-(2,3-Epoxypropyl)phthalimide
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Used as a chiral building block in organic synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and bioactive compounds. Its epoxide ring allows for regioselective ring-opening reactions with nucleophiles, enabling the introduction of functionalized side chains in drug molecules. Commonly employed in the synthesis of β-amino alcohols and as an intermediate in the production of protease inhibitors and other therapeutic agents. Also utilized in the development of chiral ligan

Used as a chiral building block in organic synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and bioactive compounds. Its epoxide ring allows for regioselective ring-opening reactions with nucleophiles, enabling the introduction of functionalized side chains in drug molecules. Commonly employed in the synthesis of β-amino alcohols and as an intermediate in the production of protease inhibitors and other therapeutic agents. Also utilized in the development of chiral ligands and catalysts for asymmetric synthesis.

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