1-Nitronaphthalene

1-Nitronaphthalene
Names
	Other names α-Nitronaphthalene
Identifiers
CAS Number	86-57-7;
3D model (JSmol)	Interactive image;
Beilstein Reference	1867714
ChEBI	CHEBI:34104;
ChEMBL	ChEMBL165373;
ChemSpider	6588;
ECHA InfoCard	100.001.531
EC Number	201-684-5;
KEGG	C14040;
PubChem CID	6849;
UNII	A51NP1DL2T;
UN number	2538
CompTox Dashboard (EPA)	DTXSID7020978;
	InChI InChI=1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H Key: RJKGJBPXVHTNJL-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)C=CC=C2[N+](=O)[O-];
Properties
Chemical formula	C10H7NO2
Molar mass	173.171 g·mol−1
Appearance	pale yellow solid
Melting point	52–61 °C (126–142 °F; 325–334 K)
Hazards
GHS pictograms
GHS Signal word	Danger
GHS hazard statements	H228, H301, H315, H319, H335, H351, H411
GHS precautionary statements	P201, P202, P210, P240, P241, P261, P264, P270, P271, P273, P280, P281, P301+310, P302+352, P304+340, P305+351+338, P308+313, P312, P321, P330, P332+313, P337+313, P362, P370+378, P391
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

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]

Safety

Toxic.

References

Booth, Gerald (2005). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411.

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[1] Booth, Gerald (2005). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411.