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Thiepane

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.

Thiepane
Names
Preferred IUPAC name
Thiepane
Identifiers
  • 4753-80-4 Y
3D model (JSmol)
  • Interactive image
ChemSpider
  • 70858 Y
ECHA InfoCard 100.022.981
EC Number
  • 225-279-8
  • 78493
UNII
  • 0P85C3FTE3 Y
  • DTXSID80197189
  • InChI=1S/C6H12S/c1-2-4-6-7-5-3-1/h1-6H2 Y
    Key: JWCVYQRPINPYQJ-UHFFFAOYSA-N Y
  • C1CCCSCC1
Properties
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).
N verify (what is YN ?)

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.

Thiepane itself may be a product of spontaneous coal fires in post-mining waste heaps.[3][n 1]

Notes edit

  1. ^ Thipeane named „hexathiophane“ in the article.

References edit

  1. ^ Yamamoto, Kagetoshi; Yamazaki, Shoko (1996). "Thiepanes and thiepins". In Newkome, George R (ed.). Thiepanes and Thiepines. Comprehensive Heterocyclic Chemistry II. Vol. 9. pp. 67–111. doi:10.1016/B978-008096518-5.00211-2. ISBN 9780080965185.{{cite encyclopedia}}: 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.
  3. ^ Kruszewski, Ł.; Fabiańska, M.J.; Ciesielczuk, J.; Segit, T.; Orłowski, R.; Motyliński, R.; Kusy, D.; Moszumańska, I. (2018). "First multi-tool exploration of a gas-condensate-pyrolysate system from the environment of burning coal mine heaps: An in situ FTIR and laboratory GC an PXRD study based on Upper Silesian materials". STOTEN. 640–641: 1044–1071. Bibcode:2018ScTEn.640.1044K. doi:10.1016/j.scitotenv.2018.05.319. PMID 30021271. S2CID 51703425.

thiepane, confused, with, thiepine, organosulfur, compound, with, formula, seven, membered, ring, heterocycles, that, contains, sulfide, parent, thiepane, seldom, been, studied, names, preferred, iupac, name, identifiers, number, 4753, model, jsmol, interactiv. Not to be confused with Thiepine 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 Thiepane Names Preferred IUPAC name Thiepane Identifiers CAS Number 4753 80 4 Y 3D model JSmol Interactive image ChemSpider 70858 Y ECHA InfoCard 100 022 981 EC Number 225 279 8 PubChem CID 78493 UNII 0P85C3FTE3 Y CompTox Dashboard EPA DTXSID80197189 InChI InChI 1S C6H12S c1 2 4 6 7 5 3 1 h1 6H2 YKey JWCVYQRPINPYQJ UHFFFAOYSA N Y SMILES C1CCCSCC1 Properties Chemical formula C 6H 12S 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 N verify what is Y N Infobox references 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 Thiepane itself may be a product of spontaneous coal fires in post mining waste heaps 3 n 1 Notes edit Thipeane named hexathiophane in the article References edit Yamamoto Kagetoshi Yamazaki Shoko 1996 Thiepanes and thiepins In Newkome George R ed Thiepanes and Thiepines Comprehensive Heterocyclic Chemistry II Vol 9 pp 67 111 doi 10 1016 B978 008096518 5 00211 2 ISBN 9780080965185 a href Template Cite encyclopedia html title Template Cite encyclopedia cite encyclopedia a CS1 maint multiple names authors list link Feher F Lex J 1976 Kristall und Moleculstrukturen von Hexathiepan S6CH2 Pentathiepan S5CH2 und Dibenzylpentathian S5C CH2C6H5 2 Z Anorg Allg Chem 423 103 111 doi 10 1002 zaac 19764230203 Kruszewski L Fabianska M J Ciesielczuk J Segit T Orlowski R Motylinski R Kusy D Moszumanska I 2018 First multi tool exploration of a gas condensate pyrolysate system from the environment of burning coal mine heaps An in situ FTIR and laboratory GC an PXRD study based on Upper Silesian materials STOTEN 640 641 1044 1071 Bibcode 2018ScTEn 640 1044K doi 10 1016 j scitotenv 2018 05 319 PMID 30021271 S2CID 51703425 nbsp This article about a heterocyclic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Thiepane amp oldid 1220206088, wikipedia, wiki, book, books, library,

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