(S)-1-((Benzyloxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid

98%

Reagent Code: #234992
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CAS Number 150407-69-5

science Other reagents with same CAS 150407-69-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 364.39 g/mol
Formula C₁₈H₂₄N₂O₆
thermostat Physical Properties
Boiling Point 518.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected functional groups allow selective deprotection and coupling in peptide-like structures, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where a piperazine scaffold is needed. The compound’s orthogonal protecting groups enable stepwise assembly in solid-phase and solution-phase synthesis, enhancing its utility in drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,460.00
inventory 250mg
10-20 days ฿6,950.00
inventory 1g
10-20 days ฿12,610.00
(S)-1-((Benzyloxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected functional groups allow selective deprotection and coupling in peptide-like structures, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where a piperazine scaffold is needed. The compound’s orthog

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected functional groups allow selective deprotection and coupling in peptide-like structures, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where a piperazine scaffold is needed. The compound’s orthogonal protecting groups enable stepwise assembly in solid-phase and solution-phase synthesis, enhancing its utility in drug discovery and development.

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