| Weight | 108.184 g/mol |
|---|---|
| Formula | C8H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,3-CYCLOOCTADIENE (29965-97-7, 1700-10-3)
1,5-COD · 1,3-COD · 1,3-cis-cis-cyclooctadiene
Score:
#225 in Materials science
,
#1498 in Physics
,
#4415 in Chemistry
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- Sigma-Aldrich - 1,3-CYCLOOCTADIENE46.80 - 95.80 USD
- Fisher Scientific - Search for 1,3-CYCLOOCTADIENE
- TCI - 1,3-CYCLOOCTADIENE82.00 - 679.00 USD
- 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)
- Ruthenium Tris(pyrazolyl)borate Complexes. 1. Synthesis and Reactivity of Ru(HB(pz)3)(COD)X (X = Cl, Br) and Ru(HB(pz)3)(L2)Cl (L = Nitrogen and Phosphorus Donor Ligands) (Organometallics, 1996)
- Cyclic hydroboration of 1,5-cyclooctadiene. A simple synthesis of 9-borabicyclo[3.3.1]nonane, an unusually stable dialkylborane (Journal of the American Chemical Society, 1968)
- Partial hydrogenation of 1,3-cyclooctadiene using dendrimer-encapsulated PdRh bimetallic nanoparticles (Journal of Molecular Catalysis A-chemical, 2003)
- C2-Symmetric bicyclo[3.3.1]nona-2,6-diene and bicyclo[3.3.2]deca-2,6-diene: new chiral diene ligands based on the 1,5-cyclooctadiene framework (Tetrahedron-asymmetry, 2005)
- Bis(1-3:5-6--cyclooctadienyl)ruthenium: Preparation, NMR spectroscopy, and isomerization to (6-1,3,5-cyclooctatriene)(1-2:5-6--1,5-cyclooctadiene)ruthenium via the activation of a CH bond (Journal of Organometallic Chemistry, 1984)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,5-COD
- 1,3-COD
- 1,3-cis-cis-cyclooctadiene
- 1,4-COD
-
SMILESC1CCC=CC=CC1
-
InChIKeyRRKODOZNUZCUBN-UHFFFAOYSA-N
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