Cyclodecanol

from Wikipedia, the free encyclopedia
Structural formula
Structural formula of cyclodecanol
General
Surname Cyclodecanol
Molecular formula C 10 H 20 O
External identifiers / databases
CAS number 1502-05-2
PubChem 15166
Wikidata Q20054511
properties
Molar mass 156.27 g mol −1
Physical state

firmly

density

0.96 g cm −3

Melting point

42 ° C

boiling point

125 ° C

solubility

soluble in ethanol

Refractive index

1.4926 (20 ° C)

safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Cyclodecanol is a chemical compound from the group of cycloalkanols .

Extraction and presentation

Cyclodecanol can be obtained by oxidizing cyclodecane .

properties

Cyclodecanol is a colorless solid. It has a monoclinic crystal structure with the space group P 2 1 / n (space group no. 14, position 2) . Template: room group / 14.2

use

Cyclodecanol can be used to make other chemical compounds such as cyclodecene or cycodecanone .

Individual evidence

  1. a b c d e f William M. Haynes: CRC Handbook of Chemistry and Physics, 95th Edition: . CRC Press, 2014, ISBN 978-1-4822-0868-9 , pp. 3–133 ( limited preview in Google Book search).
  2. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  3. ^ R. Daniel Little, Norman L. Weinberg: Electroorganic Synthesis: Festschrift for Manuel M. Baizer . CRC Press, 1991, ISBN 978-0-8247-8584-0 , pp. 172 ( limited preview in Google Book search).
  4. ^ EJ Valente, DM Pawar, EA Noe: Cyclodecanol. In: Acta Crystallographica Section C Crystal Structure Communications. 54, 1998, p. 1302, doi : 10.1107 / S0108270198003308 .
  5. ^ Howard F. Rase: Handbook of Commercial Catalysts: Heterogeneous Catalysts . CRC Press, 2000, ISBN 978-1-4200-3654-1 , pp. 87 ( limited preview in Google Book search).
  6. V. Dragutan, R. yield: Catalytic Polymerization of cyclic olefin: Ionic, Ziegler-Natta and ring-opening metathesis polymerization . Elsevier, 2000, ISBN 978-0-08-052862-5 , pp. 48 ( limited preview in Google Book search).