| Identification | Back Directory | [Name]
D-NORVALINOL | [CAS]
80696-30-6 | [Synonyms]
H-D-NVA-OL
D-NORVALINOL
(R)-2-Aminopentanol
(R)-2-AMinopentan-1-ol
D-NORVALINOL USP/EP/BP
(2R)-2-aminopentan-1-ol
2-Amino-(2R)-1-pentanol
(R)-(-)-2-AMINO-1-PENTANOL
(2R)-2-AMino-1-pentanol HCl
1-Pentanol, 2-amino-, (2R)-
(2R)-2-Amino-1-pentanol hydrochloride | [Molecular Formula]
C5H13NO | [MDL Number]
MFCD02683228 | [MOL File]
80696-30-6.mol | [Molecular Weight]
103.16 |
| Chemical Properties | Back Directory | [Melting point ]
44-48 °C(lit.) | [Fp ]
204 °F | [storage temp. ]
2-8°C(protect from light) | [Optical Rotation]
[α]20/D 17°, c = 1 in chloroform | [InChI]
1S/C5H13NO/c1-2-3-5(6)4-7/h5,7H,2-4,6H2,1H3/t5-/m1/s1 | [InChIKey]
ULAXUFGARZZKTK-RXMQYKEDSA-N | [SMILES]
CCC[C@@H](N)CO |
| Hazard Information | Back Directory | [Uses]
(R)-(-)-2-Amino-1-pentanol can be used as a chiral building block to prepare:
- A key intermediate, (R)-N-(p-toluenesulfonyl)-2-propylaziridine, which is utilized in the total synthesis of (R)-1-(benzofuran-2-yl)-2-propylaminopentane.
- (R)-N-benzyloxycarbonyl-aminoaldehydes as potential substrates for dihydroxyacetone phosphate (DHAP)-dependent aldolases.
- (R)-2-((2-Aminoquinazolin-4-yl)amino)pentan-1-ol as a potent dual toll-like receptor and modulator.
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