1,7-Octadiene, 97%
1,7-Octadiene, 97%
1,7-Octadiene, 97%
Thermo Scientific Chemicals

1,7-Octadiene, 97%

CAS: 3710-30-3 | C8H14 | 110.20 g/mol
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500 mL
產品號碼 L07659.AP
亦稱為 L07659-AP
價格 (TWD)
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Quantity:
500 mL
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化學識別
CAS3710-30-3
IUPAC Nameocta-1,7-diene
Molecular FormulaC8H14
InChI KeyXWJBRBSPAODJER-UHFFFAOYSA-N
SMILESC=CCCCCC=C
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規格Specification Sheet規格表
Appearance (Color)Clear,colourless to pale yellow
FormLiquid
Refractive Index1.4200-1.4250 @20?C
Assay (GC)>96.0%
1,7-Octadiene is used in organic synthesis. It is also used to study and assess the structure and reaction rate in olefin ring-closing metathesis of a series of simple dienes. Further, it is used in a study to investigate micropatterned surfaces prepared by plasma polymerization. It acts as a crosslinker as well as a source of ethylene in cross-enyne metathesis (CEYM)-related reactions.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,7-Octadiene is used in organic synthesis. It is also used to study and assess the structure and reaction rate in olefin ring-closing metathesis of a series of simple dienes. Further, it is used in a study to investigate micropatterned surfaces prepared by plasma polymerization. It acts as a crosslinker as well as a source of ethylene in cross-enyne metathesis (CEYM)-related reactions.

Solubility
Miscible with methanol and cyclohexane. Slightly miscible with water.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Bykov, V. I.; Chernova, O. B.; Belyaev, B. A.; Butenko, T. A.; Finkelshtein, E. S. Stereochemical features of 1,7-octadiene metathesis on the MoCl5/SiO2-Me4Sn catalytic system. Pet. Chem. 2015, 55 (7), 549-551.
  2. Apisuk, W.; Nomura, K. Efficient Terpolymerization of Ethylene and Styrene with 1,7-Octadiene by Aryloxo Modified Half-Titanocenes-Cocatalyst Systems: Efficient Introduction of the Reactive Functionality. Macromol. Chem. Phys. 2014, 215 (18), 1785-1791.