(9H-Fluoren-9-yl)methyl 3-hydroxyazetidine-1-carboxylate
97%
Reagent
Code: #113388
CAS Number
886510-13-0
blur_circular Chemical Specifications
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Molecular Information
Weight
295.33 g/mol
Formula
C₁₈H₁₇NO₃
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Registry Numbers
MDL Number
MFCD08437604
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Physical Properties
Boiling Point
488.9°C at 760 mmHg
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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.
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(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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