O-Allylhydroxylamine Hydrochloride
≥98 %
Reagent
Code: #56384
CAS Number
38945-21-0
blur_circular Chemical Specifications
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Molecular Information
Weight
109.55 g/mol
Formula
C₃H₇NOHCl
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Registry Numbers
MDL Number
MFCD00012957
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Physical Properties
Melting Point
~ 170°C (Lit.)
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Storage & Handling
Storage
room temperature, dry
description Product Description
O-Allylhydroxylamine Hydrochloride is widely used in organic synthesis, particularly as a reagent for the introduction of allyl groups into various chemical structures. It is commonly employed in the preparation of allylamines, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. The compound is also utilized in the synthesis of heterocycles and other complex organic molecules, where its ability to form stable intermediates plays a crucial role. Additionally, it finds application in the modification of polymers and biomolecules, enhancing their functional properties for specific industrial or research purposes. Its versatility and reactivity make it a key component in many synthetic pathways.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to off-white solid |
Purity | 97.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
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O-Allylhydroxylamine Hydrochloride
O-Allylhydroxylamine Hydrochloride is widely used in organic synthesis, particularly as a reagent for the introduction of allyl groups into various chemical structures. It is commonly employed in the preparation of allylamines, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. The compound is also utilized in the synthesis of heterocycles and other complex organic molecules, where its ability to form stable intermediates plays a crucial role. Additionally, it finds application in the modification of polymers and biomolecules, enhancing their functional properties for specific industrial or research purposes. Its versatility and reactivity make it a key component in many synthetic pathways.
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