Thiomorpholine

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
Thiomorpholine
Thiomorpholine
Thiomorpholine
File:Thiomorpholine-3D-balls.png
Names
Preferred IUPAC name
Thiomorpholine[1]
Other names
Thiamorpholine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
E number Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
UNII
  • {{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
  • InChI=1S/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2 checkY
    Key: BRNULMACUQOKMR-UHFFFAOYSA-N checkY
  • InChI=1/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2
    Key: BRNULMACUQOKMR-UHFFFAOYAQ
  • S1CCNCC1
Properties
C4H9NS
Molar mass 103.18 g·mol−1
Appearance Colorless liquid
Odor Strong odor resembling piperidine[2]
Density 1.0882 g/cm3
Boiling point 169 °C (336 °F; 442 K)[2]
Miscible[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Thiomorpholine, HN(CH2)4S, is a heterocyclic compound containing nitrogen and sulfur. It can be considered a thio analog of morpholine.

It can be prepared from cysteamine and vinyl chloride:[3]

H2NCH2CH2SH + CH2=CHCl → HN(CH2)4S + HCl

References

[edit | edit source]
  1. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ a b c Merck Index, 12th Edition, monograph 9435, p. 1587
  3. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).