| Weight | 89.138 g/mol |
|---|---|
| Formula | C4H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2-Aminobutan-1-ol (96-20-8, 13054-87-0)
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- Asymmetric reductions of ketones using lithium aluminium hydride modified with N,N-dialkyl derivatives of (R)-()-2-aminobutan-1-ol (Tetrahedron-asymmetry, 1991)
- Further enantioselective syntheses of -arylalkanamines via intermediate addition of Grignard reagents to a chiral hydrazone derived from (R)-()-2-aminobutan-1-ol (Tetrahedron-asymmetry, 1998)
- Asymmetric Michael additions of Grignard reagents to cinnamamides deriving from N-alkyl (R)-()-2-aminobutan-1-ol (Tetrahedron-asymmetry, 1992)
- The phospholipid composition of various organs from larvae of the housefly, Musca domestica, fed on normal diets and diets containing 2-aminobutan-1-ol (Comparative Biochemistry and Physiology, 1970)
- Synthesis of versatile chiral intermediates by enantioselective conjugate addition of alkenyl Grignard reagents to enamides deriving from (R)-()- or (S)-(+)-2-aminobutan-1-ol (Tetrahedron-asymmetry, 1998)
- O-Benzyl derivatives of (S)-(+) and (R)-()-2-aminobutan-1-ol as new resolving agents for racemic acids. Practical resolutions of N-acyl derivatives of phenylglycine and 4-hydroxyphenylglycine (Tetrahedron Letters, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(CO)N
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InChIKeyJCBPETKZIGVZRE-UHFFFAOYSA-N
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