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Cyclodecene

From Wikipedia, the free encyclopedia
Cyclodecene
(Z)-Cyclodecene
(E)-Cyclodecene
Names
IUPAC name
(Z)-Cyclodecene, (E)-Cyclodecene
Other names
cis-Cyclodecene, trans-Cyclodecene
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • cis Z: 213-301-9
  • InChI=1S/C10H18/c1-2-4-6-8-10-9-7-5-3-1/h1-2H,3-10H2/b2-1-
    Key: UCIYGNATMHQYCT-UPHRSURJSA-N
  • trans E: InChI=1S/C10H18/c1-2-4-6-8-10-9-7-5-3-1/h1-2H,3-10H2/b2-1+
    Key: UCIYGNATMHQYCT-OWOJBTEDSA-N
  • cis Z: C\1=C\CCCCCCCC/1
  • trans E: C1CCCC/C=C/CCC1
Properties
C10H18
Molar mass 138.254 g·mol−1
Density g/mL
Boiling point 193 °C (379 °F; 466 K)
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Flash point 59 °C (138 °F; 332 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Cyclodecene is a cycloalkene with a ten-membered ring, with two possible geometric isomers, denoted cis-cyclodecene and trans-cyclodecene, or (Z)-cyclodecene and (E)-cyclodecene.[1][2]

References

[edit]
  1. Traynham, James G.; Stone, DeWitt B.; Couvillion, John L. (1967-02-01). "A convenient synthesis of cis- and trans-cyclodecene". The Journal of Organic Chemistry. 32 (2): 510–510. doi:10.1021/jo01288a074. ISSN 0022-3263.
  2. Pawar, Diwakar M.; Noe, Eric A. (1996-01-01). "Dynamic NMR Study of trans-Cyclodecene". Journal of the American Chemical Society. 118 (50): 12821–12825. doi:10.1021/ja962666s. ISSN 0002-7863.