2,7-Dimethylnaphthalene

2,7-Dimethylnaphthalene
Names
	Preferred IUPAC name 2,7-Dimethylnaphthalene
Identifiers
CAS Number	582-16-1;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:48632;
ChEMBL	ChEMBL195036;
ChemSpider	10918;
ECHA InfoCard	100.008.617
EC Number	209-477-1;
PubChem CID	11396;
UNII	ON63XH5BQ4;
CompTox Dashboard (EPA)	DTXSID7060386 ;
	InChI Key: YGYNBBAUIYTWBF-UHFFFAOYSA-N;
	SMILES CC1=CC2=C(C=C1)C=CC(=C2)C;
Properties
Chemical formula	C12H12
Molar mass	156.228 g·mol−1
Appearance	white solid
Melting point	95–96 °C (203–205 °F; 368–369 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

2,7-Dimethylnaphthalene (2,7-DMN) is an organic compound with the formula C₁₀H₆(CH₃)₂. It is one of the ten isomers of dimethylnaphthalene.^[1] Alkylated naphthalenes are obtained from coal tar. It can be obtained from 2,7-dihydroxynaphthalene.^[2] It reacts with N-bromosuccinimide to give 2,7-bis(bromomethyl)naphthalene.

References

↑ Collin, Gerd; Höke, Hartmut; Greim, Helmut (2003). "Naphthalene and Hydronaphthalenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_001.pub2. ISBN 978-3-527-30673-2.
↑ Dallaire, Carol; Kolber, Isabelle; Gingras, Marc (2002). "Nickel-Catalyzed Coupling of Aryl O-Carbamates with Grignard Reagents: 2,7-Dimethylnaphthalene". Organic Syntheses. 78: 42. doi:10.15227/orgsyn.078.0042.

[1] Collin, Gerd; Höke, Hartmut; Greim, Helmut (2003). "Naphthalene and Hydronaphthalenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_001.pub2. ISBN 978-3-527-30673-2.

[2] Dallaire, Carol; Kolber, Isabelle; Gingras, Marc (2002). "Nickel-Catalyzed Coupling of Aryl O-Carbamates with Grignard Reagents: 2,7-Dimethylnaphthalene". Organic Syntheses. 78: 42. doi:10.15227/orgsyn.078.0042.

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