1,5-Cyclooctadiene

CAS: 111-78-4

Ref. 3D-FC60816

Product Information

• Name: 1,5-Cyclooctadiene
• Synonyms: COD [stabilized with Octadecyl 3-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)propionate], (1E,5Z)-cycloocta-1,5-diene, (1Z,3Z)-cycloocta-1,3-diene, (1Z,5Z)-cycloocta-1,5-diene, (Z,Z)-1,5-Cyclooctadiene, 1,5-Cod, 1,5-Cyclooctadien, 1-cis-5-cis-Cyclooctadiene, 1Z,5Z-Cyclooctadiene, Ai3-26692, COD, Cicloocta-1,5-Dieno, Cycloocta-1,5-dien, Hsdb 5549, Nsc 60155, cis,cis-1,5-Cyclooctadiene, cis-1,5-Cyclooctadiene
• CAS: 111-78-4

Description

1,5-Cyclooctadiene is a substrate molecule that can be used in the preparation of sodium carbonate. The molecule has a helical structure and exhibits an x-ray absorption spectrum with a single structure. The nucleophilic attack of the chloride ion on the carbonyl group leads to the formation of an intermediate which is then oxidized to produce 1,5-cyclooctadienesulfonic acid. The reaction mechanism for this process involves coordination geometry and molecular orbital theory. 1,5-Cyclooctadiene is also used as a starting point for the synthesis of palladium complexes and naphthalenes. This molecule has been shown to exhibit NMR spectra that are characteristic of p2 groups.

• Brand: Biosynth

Chemical properties

• Molecular weight: 108.18 g/mol
• Formula: C₈H₁₂
• Purity: Min. 95%
• Color/Form: Clear Liquid
• InChI: InChI=1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-2,7-8H,3-6H2/b2-1-,8-7-
• InChI key: InChIKey=VYXHVRARDIDEHS-QGTKBVGQSA-N
• SMILES: C1=C\CC/C=C\CC/1