Thiepane

Thiepane
Structural formula of thiepane	Ball-and-stick model of the thiepane molecule
Names
	IUPAC name Thiepane
Identifiers
CAS Number	4753-80-4 ;
3D model (JSmol)	Interactive image;
ChemSpider	70858 ;
ECHA InfoCard	100.022.981
EC Number	225-279-8;
PubChem CID	78493;
UNII	0P85C3FTE3 ;
CompTox Dashboard (EPA)	DTXSID80197189 ;
	InChI InChI=1S/C6H12S/c1-2-4-6-7-5-3-1/h1-6H2 Key: JWCVYQRPINPYQJ-UHFFFAOYSA-N ;
	SMILES C1CCCSCC1;
Properties
Chemical formula	C6H12S
Molar mass	116.22 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Thiepane is the organosulfur compound with the formula (CH₂)₆S. Thiepanes are seven-membered ring heterocycles that contains sulfide.[1] The parent thiepane has seldom been studied.

A variety of derivatives are known. Hexathiathiepane (CAS RN 17233-71-5, m.p. 90 °C) is CH₂S₆.[2] A naturally occurring derivative is lenthionine, 1,4-(CH₂)₂S₅.

Reference

Yamamoto, Kagetoshi; Yamazaki, Shoko (1996). "Thiepanes and thiepins". In Newkome, George R (ed.). Comprehensive Heterocyclic Chemistry II. 9. pp. 67–111. doi:10.1016/B978-008096518-5.00211-2.CS1 maint: multiple names: authors list (link)
Fehér, F.; Lex, J. (1976). "Kristall- und Molecülstrukturen von Hexathiepan (S₆CH₂), Pentathiepan (S₅CH₂) und Dibenzylpentathian (S₅C(CH₂C₆H₅)₂)". Z. anorg. allg. Chem. 423: 103–111. doi:10.1002/zaac.19764230203.CS1 maint: uses authors parameter (link)

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[1] Yamamoto, Kagetoshi; Yamazaki, Shoko (1996). "Thiepanes and thiepins". In Newkome, George R (ed.). Comprehensive Heterocyclic Chemistry II. 9. pp. 67–111. doi:10.1016/B978-008096518-5.00211-2.CS1 maint: multiple names: authors list (link)

[2] Fehér, F.; Lex, J. (1976). "Kristall- und Molecülstrukturen von Hexathiepan (S₆CH₂), Pentathiepan (S₅CH₂) und Dibenzylpentathian (S₅C(CH₂C₆H₅)₂)". Z. anorg. allg. Chem. 423: 103–111. doi:10.1002/zaac.19764230203.CS1 maint: uses authors parameter (link)