Names | |
---|---|
Preferred IUPAC name
1-Nitronaphthalene | |
Other names
α-Nitronaphthalene
| |
Identifiers | |
3D model (
JSmol)
|
|
1867714 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.001.531 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
UN number | 2538 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C10H7NO2 | |
Molar mass | 173.171 g·mol−1 |
Appearance | pale yellow solid |
Density | 1.332 g/cm3 |
Melting point | 52–61 °C (126–142 °F; 325–334 K) |
Boiling point | 304 °C (579 °F; 577 K) |
Hazards | |
GHS labelling: | |
Danger | |
H228, H301, H315, H319, H335, H351, H411 | |
P201, P202, P210, P240, P241, P261, P264, P270, P271, P273, P280, P281, P301+P310, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P370+P378, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1-Nitronaphthalene is an organic compound with the formula C10H7NO2. It is one of two isomers of nitronaphthalene. A pale yellow, sublimable solid, 1-nitronaphthalene is the main product of the direct nitration of naphthalene. It is an intermediate in the production of naphthylamine, a precursor to dyes. [1] The conversion to the amine is effected by hydrogenation. [2]
Its -log LC50 is 4.49 for fathead minnows. [3]