(9H-Fluoren-9-yl)methyl 3-hydroxyazetidine-1-carboxylate

97%

Reagent Code: #113388
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CAS Number 886510-13-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₈H₁₇NO₃
badge Registry Numbers
MDL Number MFCD08437604
thermostat Physical Properties
Boiling Point 488.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a protective group for amines and hydroxyl groups during complex chemical reactions. Its fluorenylmethyl moiety offers stability under various reaction conditions, making it a valuable tool in peptide synthesis and the preparation of pharmaceuticals. The azetidine ring contributes to its versatility, allowing it to participate in cyclization and ring-opening reactions, which are essential in constructing biologically active molecules. Additionally, its use in solid-phase synthesis enables the efficient production of peptides and small molecules, aiding in drug discovery and development. Its ability to be selectively removed under mild conditions further enhances its utility in multi-step synthetic processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days €544.96
inventory 25g
10-20 days €1,779.37
inventory 1g
10-20 days €181.73
inventory 10g
10-20 days €907.95
(9H-Fluoren-9-yl)methyl 3-hydroxyazetidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as a protective group for amines and hydroxyl groups during complex chemical reactions. Its fluorenylmethyl moiety offers stability under various reaction conditions, making it a valuable tool in peptide synthesis and the preparation of pharmaceuticals. The azetidine ring contributes to its versatility, allowing it to participate in cyclization and ring-opening reactions, which are essential in constructing biologically active molecules. Additionally, its use in solid-phase synthesis enables the efficient production of peptides and small molecules, aiding in drug discovery and development. Its ability to be selectively removed under mild conditions further enhances its utility in multi-step synthetic processes.
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