O-Allylhydroxylamine Hydrochloride

≥98 %

  • Product Code: 56384
  CAS:    38945-21-0
Molecular Weight: 109.55 g./mol Molecular Formula: C₃H₇NOHCl
EC Number: MDL Number: MFCD00012957
Melting Point: ~ 170°C (Lit.) Boiling Point:
Density: Storage Condition: room temperature, dry
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.
Product Specification:
Test Specification
APPEARANCE White to off-white Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days Ft5,602.54
+
-
5.000 10-20 days Ft21,009.51
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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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