| Weight | 108.184 g/mol |
|---|---|
| Formula | C8H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,5-CYCLOOCTADIENE (111-78-4)
Score:
#212 in Materials science
,
#1429 in Physics
,
#4207 in Chemistry
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- Reactions of (-1,5-cyclooctadiene) organoplatinum(II) compounds and the synthesis of perfluoroalkylplatinum complexes (Journal of Organometallic Chemistry, 1973)
- Synthesis with zerovalent nickel. Coupling of alkenyl halides with bis(1,5-cyclooctadiene)nickel(0) (Journal of the American Chemical Society, 1971)
- DiChloroBis(41,5Cyclooctadiene)Dirhodium(I) (2007)
- Hydroboration. XXXVI. Direct route to 9-borabicyclo[3.3.1]nonane via the cyclic hydroboration of 1,5-cyclooctadiene. 9-Borabicyclo[3.3.1]nonane as a uniquely selective reagent for the hydroboration of olefins (Journal of the American Chemical Society, 1974)
- Use of the Cationic Iridium Complex 1,5-Cyclooctadiene-bis[methyldiphenylphosphine]-iridium Hexafluorophosphate in Carbohydrate Chemistry: Smooth Isomerization of Allyl Ethers to 1-Propenyl Ethers (Synthesis, 1981)
- Cyclooctene and 1,5Cyclooctadiene Complexes of Iridium(I) (2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC=CCCC=C1
-
InChIKeyVYXHVRARDIDEHS-UHFFFAOYSA-N
- Pubchem - 1,5-CYCLOOCTADIENE
- Wikipedia - 1,5-cyclooctadiene
1,5-Cyclooctadiene is the organic compound with the chemical formula C8H12. Generally abbreviated COD, this diene is a useful precursor to other organic compounds and serves as a ligand in organometallic chemistry. It is a colorless liquid with a strong odor.
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