1-N-Cbz-Pyrrolidine-3-acetic acid

96%

Reagent Code: #218089
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CAS Number 886362-65-8

science Other reagents with same CAS 886362-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₄H₁₇NO₄
badge Registry Numbers
MDL Number MFCD02179025
thermostat Physical Properties
Boiling Point 448.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its structure supports the construction of complex molecules where a protected pyrrolidine ring is required, especially in peptide-based drugs. The Cbz-protected amine allows for selective deprotection and further functionalization during multi-step syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting viral infections and metabolic disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,810.00
inventory 250mg
10-20 days ฿5,710.00
inventory 1g
10-20 days ฿13,140.00
1-N-Cbz-Pyrrolidine-3-acetic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its structure supports the construction of complex molecules where a protected pyrrolidine ring is required, especially in peptide-based drugs. The Cbz-protected amine allows for selective deprotection and further functionalization during multi-step syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its structure supports the construction of complex molecules where a protected pyrrolidine ring is required, especially in peptide-based drugs. The Cbz-protected amine allows for selective deprotection and further functionalization during multi-step syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting viral infections and metabolic disorders.

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