| Identification | Back Directory | [Name]
NITROCYCLOPENTANE | [CAS]
2562-38-1 | [Synonyms]
NITROCYCLOPENTANE
nitro-cyclopentan
1-Nitrocyclopentane
NITROCYCLOPENTANE, 97+%
(1S,2S)-Methyl 2-aMinocyclopropanecarboxylate | [EINECS(EC#)]
219-884-6 | [Molecular Formula]
C5H9NO2 | [MDL Number]
MFCD00001362 | [MOL File]
2562-38-1.mol | [Molecular Weight]
115.13 |
| Chemical Properties | Back Directory | [Appearance]
Clear pale yellow liquid | [Melting point ]
143-144 °C | [Boiling point ]
180 °C(lit.)
| [density ]
1.086 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.454(lit.)
| [Fp ]
153 °F
| [form ]
liquid | [pka]
8.46±0.20(Predicted) | [BRN ]
907079 | [CAS DataBase Reference]
2562-38-1 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear pale yellow liquid | [Preparation]
Bromocyclopentane (22.0 g, 0.15 mol) was added to a soln of NaNO2 (18 g, 0.26 mol) in dry DMSO (100 mL) at 15 ℃ and the mixture was stirred at this temperature for 3 h. The mixture was poured into ice water (250 mL) and extracted with petroleum ether (bp 35-37 ℃; 4 × 50 mL). The combined organic extracts were washed with H2O (4× 50 mL), dried (MgSO4), and concentrated under reduced pressure. The residue was distilled to give Nitrocyclopentane; yield: 9.9 g (58%); bp 62 ℃/8 Torr; nD/20 1.4538.
Synthesis of Nitrocyclopentane | [Synthesis Reference(s)]
Tetrahedron Letters, 21, p. 1117, 1980 DOI: 10.1016/S0040-4039(01)83928-9 | [General Description]
Nitrocyclopentane, a secondary nitroalkane, was examined for its ability to induce DNA repair in rat hepatocytes. The nitronate of nitrocyclopentane was mutagenic in Salmonella strains TA100 and TA102. |
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