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cis-Cyclooctene

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CAS:931-88-4
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Products Intro: Product Name:cis-Cyclooctene
CAS:931-88-4
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cis-Cyclooctene manufacturers

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  • CAS:931-88-4
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  • Cyclooctene
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  • 2020-01-07
  • CAS: 931-88-4
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  • cis-Cyclooctene
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  • 2019-12-24
  • CAS:931-88-4
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cis-Cyclooctene Basic information
Product Name:cis-Cyclooctene
Synonyms:CIS-CYCLOOCTENE;Cyclooctene,99%;CYCLOOCTENE 95%;CYCLOOCTENE, STANDARD FOR GC;CYCLOOCTENE;Cyclooctene >;cis-Cyclooctene ISO 9001:2015 REACH;Cyclooctene in Acetonitrile
CAS:931-88-4
MF:C8H14
MW:110.2
EINECS:213-245-5
Product Categories:Alpha Sort;C;CAlphabetic;CO - CZChemical Class;Hydrocarbons;NeatsGasoline, Diesel,&Petroleum;Olefins;Substance classes;Volatiles/ Semivolatiles
Mol File:931-88-4.mol
cis-Cyclooctene Structure
cis-Cyclooctene Chemical Properties
Melting point −16 °C(lit.)
Boiling point 32-34 °C12 mm Hg(lit.)
density 0.848 g/mL at 20 °C(lit.)
refractive index n20/D 1.470
Fp 77 °F
Water Solubility Insoluble in water
color Colorless to Almost colorless
BRN 1901031
LogP3.930
CAS DataBase Reference931-88-4(CAS DataBase Reference)
NIST Chemistry ReferenceCyclooctene(931-88-4)
EPA Substance Registry SystemCyclooctene (931-88-4)
Safety Information
Hazard Codes Xn
Risk Statements 10-65
Safety Statements 29-33-62-16
RIDADR UN 3295 3/PG 3
WGK Germany 3
TSCA TSCA listed
HS Code 2902.19.0050
HazardClass 3.2
PackingGroup III
MSDS Information
ProviderLanguage
cis-Cyclooctene English
ACROS English
SigmaAldrich English
ALFA English
cis-Cyclooctene Usage And Synthesis
Purification MethodsThe cis-isomer is freed from the trans-isomer by fractional distillation through a spinning-band column, followed by preparative gas chromatography on a Dowex 710-Chromosorb W GLC column. It is passed through a short alumina column immediately before use [Collman et al. J Am Chem Soc 108 2588 1986]. It has also been distilled in a dry N2 glove box from powdered fused NaOH through a Vigreux column (p 11), then passed through activated neutral alumina before use [Wong et al. J Am Chem Soc 109 4328 1987]. Alternatively it can be purified via the AgNO3 salt. This salt is obtained from crude cyclooctene (40 mL) by shaking at 70-80o with 50% w/w AgNO3 (2 x 15 mL) to remove cyclooctadienes (aqueous layer). Extraction is repeated at 40o (4 x 20 mL, of 50% AgNO3). Three layers are formed each time. The middle layer contains the AgNO3 adduct of cyclooctene which crystallises on cooling the layer to room temperature. The adduct (complex 2:1) is highly soluble in MeOH (at least 1g/mL) from which it crystallises in large flat needles when cooled at 0o. It is dried under slight vacuum for 1 week in the presence of CaCl2 and paraffin wax soaked in cyclooctene. It has m 51o and loses hydrocarbon on exposure to air. cis-Cyclooctene can be recovered by steam distillation of the salt, collected, dried (CaCl2) and distilled in vacuum. [Braude et al. J Chem Soc 4711 1957, AgNO3: Jones J Chem Soc 1808 1954, Cope & Estes J Am Chem Soc 72 1128 1950, Beilstein 5 I 35, 5 IV 263.] FLAMMABLE LIQUID.
cis-Cyclooctene Preparation Products And Raw materials
Raw materials1,3-CYCLOOCTADIENE
Tag:cis-Cyclooctene(931-88-4) Related Product Information
Ionone (Z)-1-Cyclooctene,cis-Cyclooctene,94%,cis-Cyclooctene, stabilized, 95%,cis-Cyclooctene, 95%, stab.,Cis-Cyclooctene, 95%, stabilized 6H,12H-5,11-Dioxadibenzo[a,e]cyclooctene-6,12-dione CYCLOOCTYL BROMIDE 2,2,6-Trimethyl-4H-1,3-dioxin-4-one Bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate (5S)-6α,7β-Dimethyl-1,2,3,12-tetramethoxy-10,11-methylenedioxy(5,6,7,8-tetrahydrodibenzo[a,c]cyclooctene)-5α,6β-diol 5-benzoate 6,7,8,9,10,11-HEXAHYDRO-5H-CYCLOOCTA[B]INDOLE CYCLOOCTENE OXIDE 1,2-EPOXY-5-CYCLOOCTENE Chlorobis(cyclooctene)rhodium(I) dimer Dibenzo[a,e]cyclooctene 5,6,11,12-Tetrahydrodibenzo[a,e]cyclooctene 1-METHYL-1-CYCLOOCTENE cis-Cyclooctene oxide 1,2-Epoxy-7-cyclooctene 1-Cyclooctene-3-ol,Cyclooctene-3-ol cis-Cyclooctene

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