(S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropyl 4-methylbenzenesulfonate

≥95%

Reagent Code: #235690
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CAS Number 141403-49-8

science Other reagents with same CAS 141403-49-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.51 g/mol
Formula C₂₁H₂₇NO₅S
badge Registry Numbers
MDL Number MFCD22571764
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of biologically active molecules, particularly in the preparation of peptidomimetics and pharmaceuticals. Its chiral center and protected amine group make it valuable in asymmetric synthesis, where stereochemistry is critical. The tosylate group acts as a good leaving group, enabling nucleophilic substitution reactions to introduce various functional groups. Commonly employed in the development of enzyme inhibitors and receptor ligands, especially in research targeting protease inhibitors and central nervous system agents. Widely utilized in medicinal chemistry for building complex molecules with high enantiomeric purity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,970.00
inventory 250mg
10-20 days ฿10,150.00
inventory 1g
10-20 days ฿29,660.00
(S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropyl 4-methylbenzenesulfonate
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Used as a key intermediate in the synthesis of biologically active molecules, particularly in the preparation of peptidomimetics and pharmaceuticals. Its chiral center and protected amine group make it valuable in asymmetric synthesis, where stereochemistry is critical. The tosylate group acts as a good leaving group, enabling nucleophilic substitution reactions to introduce various functional groups. Commonly employed in the development of enzyme inhibitors and receptor ligands, especially in research t

Used as a key intermediate in the synthesis of biologically active molecules, particularly in the preparation of peptidomimetics and pharmaceuticals. Its chiral center and protected amine group make it valuable in asymmetric synthesis, where stereochemistry is critical. The tosylate group acts as a good leaving group, enabling nucleophilic substitution reactions to introduce various functional groups. Commonly employed in the development of enzyme inhibitors and receptor ligands, especially in research targeting protease inhibitors and central nervous system agents. Widely utilized in medicinal chemistry for building complex molecules with high enantiomeric purity.

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