| Weight | 123.155 g/mol |
|---|---|
| Formula | C7H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
O-Benzylhydroxylamine (622-33-3)
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- Chiral Lewis Acid Catalysis in Conjugate Additions of O-Benzylhydroxylamine to Unsaturated Amides. Enantioselective Synthesis of -Amino Acid Precursors (Journal of the American Chemical Society, 1998)
- Asymmetric titanium-catalysed Michael addition of O-benzylhydroxylamine to -unsaturated carbonyl compounds: synthesis of -amino acid precursors (Journal of The Chemical Society-perkin Transactions 1, 1996)
- Organocatalytic asymmetric aza-Michael reaction : enantioselective addition of O -benzylhydroxylamine to chalcones (Tetrahedron Letters, 2007)
- Derivatization of the tricarboxylic acid intermediates with O-benzylhydroxylamine for liquid chromatography-tandem mass spectrometry detection. (Analytical Biochemistry, 2014)
- Samarium Iodobinaphtholate: An Efficient Catalyst for Enantioselective Aza-Michael Additions of O-Benzylhydroxylamine to N-Alkenoyloxazolidinones (European Journal of Organic Chemistry, 2011)
- N(Diethoxyphosphoryl)Obenzylhydroxylamine A Convenient Substrate for the Synthesis of NSubstituted OBenzylhydroxylamines. (Tetrahedron, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)CON
-
InChIKeyXYEOALKITRFCJJ-UHFFFAOYSA-N
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O-Benzylhydroxylamine
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