| Weight | 103.165 g/mol |
|---|---|
| Formula | C5H13NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
16369-05-4
valinol · (+-)-isomer of valinol · 2-amino-3-methyl-1-butanol
16369-05-4, 2026-48-4, 473-75-6
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LabBot
- Mixed Aggregates Containing n-Butyl-, sec-Butyl-, or tert-Butyllithium and a Chiral Lithium Amide Derived from N-Isopropyl-O-methyl Valinol (Journal of the American Chemical Society, 1997)
- A Novel Proline-Valinol Thioamide Small Organic Molecule for a Highly Enantioselective Direct Aldol Reaction (Advanced Synthesis & Catalysis, 2009)
- N1,N10-Ethylene-bridged flavinium salts derived from l-valinol: synthesis and catalytic activity in H2O2 oxidations (Tetrahedron Letters, 2010)
- L-Valinol and L-phenylalaninol-derived 2-phenylamino-2-oxazolines as chiral auxiliaries in asymmetric alkylations (Tetrahedron-asymmetry, 2002)
- Two Modes of Asymmetric Polymerization of Phenylacetylene Having a l-Valinol Residue and Two Hydroxy Groups (Journal of Polymer Science Part A, 2009)
- Characterization of Dimeric Chiral Lithium Amide Structures Derived from N-isopropyl-O- triisopropylsilyl Valinol (Journal of the American Chemical Society, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - valinol
- (+-)-isomer of valinol
- 2-amino-3-methyl-1-butanol
-
SMILESCC(C)C(CO)N
-
InChIKeyNWYYWIJOWOLJNR-UHFFFAOYSA-N
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16369-05-4
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