- CYCLOOCTENE
-
- $100.00 / 1KG
-
2023-12-26
- CAS:931-87-3
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
|
| | CYCLOOCTENE Basic information |
| Product Name: | CYCLOOCTENE | | Synonyms: | cis-Cyclooctene contains 100-200 ppM Irganox 1076 FD as antioxidant, 95%;(1Z)-Cyclooctene;1-Cyclooctene;Cyclooctene, (Z)-;CYCLOOCTENE;cis-Cyclooctene, stabilized, 95%;Cyclooctene, (1Z)-;(Z)-Cycloocten | | CAS: | 931-87-3 | | MF: | C8H14 | | MW: | 110.2 | | EINECS: | 213-243-4 | | Product Categories: | Alkenes;Cyclic;Organic Building Blocks | | Mol File: | 931-87-3.mol |  |
| | 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.) | | vapor pressure | 9.9hPa at 20℃ | | refractive index | n20/D 1.470 | | Fp | 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) |
| 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 |
| | CYCLOOCTENE Usage And Synthesis |
| 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 |
|