2-Naphthalenethiol

2-Naphthalenethiol
Names
	IUPAC name Naphthalene-2-thiol
Identifiers
CAS Number	91-60-1;
3D model (JSmol)	Interactive image;
ChemSpider	6791;
ECHA InfoCard	100.001.893
EC Number	202-082-5;
PubChem CID	7058;
UNII	SZ5U1S741V;
CompTox Dashboard (EPA)	DTXSID1059028 ;
	InChI InChI=1S/C10H8S/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H Key: RFCQDOVPMUSZMN-UHFFFAOYSA-N;
	SMILES C1=CC=C2C=C(C=CC2=C1)S;
Properties
Chemical formula	C10H8S
Molar mass	160.23 g·mol−1
Appearance	White solid
Melting point	80–81 °C (176–178 °F; 353–354 K)
Boiling point	92–94 °C (198–201 °F; 365–367 K) (at 0.4 mmHg)
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H302
GHS precautionary statements	P264, P270, P301+312, P330, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

2-Naphthalenethiol is an organosulfur compound with the formula C₁₀H₇SH. It is a white solid. It is one of two monothiols of naphthalene, the other being 1-naphthalenethiol.

Synthesis and reactions

2-Naphthalenethiol is prepared from 2-naphthol by the Newman–Kwart rearrangement using the thiocarbamate.[1] It undergoes lithiation at the 1 and 3-position.[2][3]

It can be used as a flavouring agent.[4]

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References

Melvin S. Newman; Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227/orgsyn.051.0139.
Block, E.; Eswarakrishnan, V.; Gernon, M.; Ofori-Okai, G.; Saha, C.; Tang, K.; Zubieta, J. (1989). "o-Lithiothiophenol Equivalents. Generation, Reactions and Applications in Synthesis of Hindered Thiolate Ligands". J. Am. Chem. Soc. 111: 658–665. doi:10.1021/ja00184a039.
Still, Ian WJ; Natividad-Preyra, Rosanne; Toste, F Dean (1999). "A versatile synthetic route to 1,5-dithiocins from o-mercapto aromatic aldehydes". Canadian Journal of Chemistry. 77: 113–121. doi:10.1139/v98-230.
WHO, World Health. "Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA) Feedback Print preview Link to this page 2-NAPHTHALENETHIOL". apps.who.int. Retrieved 15 January 2018.

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[1] Melvin S. Newman; Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227/orgsyn.051.0139.

[2] Block, E.; Eswarakrishnan, V.; Gernon, M.; Ofori-Okai, G.; Saha, C.; Tang, K.; Zubieta, J. (1989). "o-Lithiothiophenol Equivalents. Generation, Reactions and Applications in Synthesis of Hindered Thiolate Ligands". J. Am. Chem. Soc. 111: 658–665. doi:10.1021/ja00184a039.

[DT-3] Still, Ian WJ; Natividad-Preyra, Rosanne; Toste, F Dean (1999). "A versatile synthetic route to 1,5-dithiocins from o-mercapto aromatic aldehydes". Canadian Journal of Chemistry. 77: 113–121. doi:10.1139/v98-230.

[4] WHO, World Health. "Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA) Feedback Print preview Link to this page 2-NAPHTHALENETHIOL". apps.who.int. Retrieved 15 January 2018.