| Weight | 75.111 g/mol |
|---|---|
| Formula | C3H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
L-Alaninol (2749-11-3)
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- Transformation of Isopropylamine to l-Alaninol by Pseudomonas sp. Strain KIE171 Involves N-Glutamylated Intermediates (Applied and Environmental Microbiology, 2002)
- Kinetics of the Aqueous-Phase Hydrogenation of l-Alanine to l-Alaninol (Industrial & Engineering Chemistry Research, 2004)
- A new electrophilic alaninol synthon. A general route to oxazolidinones of D or (R)-2-amino alcohols from L-serine (Journal of The Chemical Society-perkin Transactions 1, 1994)
- Synthesis, solvatochromic properties, and dipole moments of Fmoc-l-alaninol (Journal of Molecular Liquids, 2014)
- Preparation and Circular Dichroism of L(+)-Alaninol Cobalt(III) Complex (Bulletin of the Chemical Society of Japan, 1967)
- Synthese du L-alaninol a partir d'extraits acellulaires de Mycobacterium avium (FEBS Letters, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(CO)N
-
InChIKeyBKMMTJMQCTUHRP-UHFFFAOYSA-N
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L-Alaninol
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