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CYCLOOCTENE

Product Name
CYCLOOCTENE
CAS No.
931-87-3
Chemical Name
CYCLOOCTENE
Synonyms
(Z)-cyclooctene;CYCLOOCTENE;1-Cyclooctene;(Z)-Cycloocten;(1Z)-Cyclooctene;Cyclooctene ,95%;Cyclooctene, (Z)-;(Z)-1-Cyclooctene;Cyclooctene, (1Z)-;cis-Cyclooctene,94%
CBNumber
CB7340240
Molecular Formula
C8H14
Formula Weight
110.2
MOL File
931-87-3.mol
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CYCLOOCTENE Property

Melting point:
−16 °C(lit.)
Boiling point:
32-34 °C12 mm Hg(lit.)
Density 
0.848 g/mL at 20 °C(lit.)
vapor pressure 
9.9hPa at 20℃
refractive index 
n20/D 1.470
Flash point:
77 °F
storage temp. 
Flammables area
solubility 
H2O: insoluble
form 
Liquid
color 
Clear colorless to light brown
Water Solubility 
Miscible with alcohol and ether. Immiscible with water.
Sensitive 
Air Sensitive
BRN 
1280166
LogP
5 at 25℃
CAS DataBase Reference
931-87-3(CAS DataBase Reference)
EPA Substance Registry System
Cyclooctene, (1Z)- (931-87-3)
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Safety

Hazard Codes 
Xn
Risk Statements 
10-65
Safety Statements 
29-33
RIDADR 
UN 3295 3/PG 3
WGK Germany 
3
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29021990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H226Flammable liquid and vapour

H304May be fatal if swallowed and enters airways

H401Toxic to aquatic life

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
125482
Product name
cis-Cyclooctene
Purity
contains 100-200 ppm Irganox 1076 FD as antioxidant, 95%
Packaging
25ml
Price
$55.9
Updated
2024/03/01
Alfa Aesar
Product number
A13477
Product name
cis-Cyclooctene, 95%, stab.
Packaging
50ml
Price
$35.65
Updated
2024/03/01
Alfa Aesar
Product number
A13477
Product name
cis-Cyclooctene, 95%, stab.
Packaging
100ml
Price
$42.65
Updated
2024/03/01
Alfa Aesar
Product number
A13477
Product name
cis-Cyclooctene, 95%, stab.
Packaging
250ml
Price
$76.65
Updated
2024/03/01
Alfa Aesar
Product number
A13477
Product name
cis-Cyclooctene, 95%, stab.
Packaging
500ml
Price
$156
Updated
2024/03/01
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CYCLOOCTENE Chemical Properties,Usage,Production

Chemical Properties

clear colourless to light brown liquid

Uses

cis-Cyclooctene is used as a displaced ligand in chlorobis(cyclooctene)rhodium dimer and chlorobis(cyclooctene)iridium dimer in organometallic chemistry. It acts as a monomer used in synthetic chemistry. It is used to prepare 1-chloro-4-(trichloromethyl) cyclooctane by reaction with carbon tetrachloride using dichlorotris(triphenylphosphine) ruthenium(II) as a catalyst. Further, it is used to study the alkenes chemisorbed on silicon(100) by scanning tunneling microscopy.

Synthesis Reference(s)

Journal of the American Chemical Society, 102, p. 2693, 1980 DOI: 10.1021/ja00528a029
The Journal of Organic Chemistry, 40, p. 2555, 1975 DOI: 10.1021/jo00905a040
Tetrahedron Letters, 14, p. 2667, 1973

General Description

cis-Cyclooctene undergoes addition reaction with carbon tetrachloride catalyzed by dichlorotris(triphenylphosphine) ruthenium(II) to yield 1-chloro-4-(trichloromethyl) cyclooctane (1,4-adduct). It undergoes epoxidation catalyzed by molybdenum oxide nanoparticles incorporated in a mesoporous silica shell coated on dense silica-coated magnetite nanoparticles.

Purification Methods

The 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.

CYCLOOCTENE Preparation Products And Raw materials

Raw materials

Preparation Products

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CYCLOOCTENE Suppliers

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View Lastest Price from CYCLOOCTENE manufacturers

Henan Fengda Chemical Co., Ltd
Product
CYCLOOCTENE 931-87-3
Price
US $100.00-1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2023-12-25
Shaanxi Dideu Medichem Co. Ltd
Product
cis-Cyclooctene, stabilized 931-87-3
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20T
Release date
2020-01-07

931-87-3, CYCLOOCTENERelated Search:


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