| Weight | 188.267 g/mol |
|---|---|
| Formula | C10H20O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 8 |
2-HYDROXYDECANOIC ACID (5393-81-7)
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- Asymmetric synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid: The unknown amino acid component of microginin (Tetrahedron-asymmetry, 1994)
- Asymmetric synthesis of the N-terminal component of microginin: (2S,3R)-3-amino-2-hydroxydecanoic acid, its (2R,3R)-epimer and (3R)-3-aminodecanoic acid (Tetrahedron-asymmetry, 1995)
- Metal halide-mediated opening of three membered rings: enantioselective synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid and (3R)-3-aminodecanoic acid (Tetrahedron-asymmetry, 1997)
- Synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid and (3R,4R)-3-amino-4-hydroxyazepane from D-isoascorbic acid (Tetrahedron-asymmetry, 1996)
- A 3-amino-10-chloro-2-hydroxydecanoic acid-containing tetrapeptide from Oscillatoria agardhii (Phytochemistry, 1997)
- Stereoselective synthesis of the nonproteinogenic amino acid (2S,3R)-3-amino-2-hydroxydecanoic acid from (4S,5S)-4-formyl-5-vinyl-2-oxazolidinone. (Journal of Organic Chemistry, 2003)
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SMILESCCCCCCCCC(C(=O)O)O
-
InChIKeyGHPVDCPCKSNJDR-UHFFFAOYSA-N
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