Weight | 66.103 g/mol |
---|---|
Formula | C5H6 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Cyclopentadiene (542-92-7)
1,3-cyclopentadiene
Score:
#572 in Physics
,
#1665 in Chemistry
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- The Electron Diffraction Investigation of the Structure of Benzene, Pyridine, Pyrazine, Butadiene-1,3, Cyclopentadiene, Furan, Pyrrole, and Thiophene (Journal of the American Chemical Society, 1939)
- Role reversal in the cyclocondensation of cyclopentadiene with heterodienophiles derived from aryl amines and aldehydes: synthesis of novel tetrahydroquinolines (Tetrahedron Letters, 1988)
- Theoretical Study of the Electronic Structure of 2,2-Bisilole in Comparison with 1,1-Bi-1,3-cyclopentadiene: ** Conjugation and a Low-Lying LUMO as the Origin of the Unusual Optical Properties of 3,3,4,4-Tetraphenyl-2,2-bisilole (Bulletin of the Chemical Society of Japan, 1996)
- Theoretical study of the electronic spectra of cyclopentadiene, pyrrole, and furan (Journal of the American Chemical Society, 1993)
- On the Ti-TADDOLate-Catalyzed Diels-Alder Addition of 3-Butenoyl-1,3-oxazolidin-2-one to Cyclopentadiene. General Features of Ti-BINOLate- and Ti-TADDOLate-Mediated Reactions (Journal of Organic Chemistry, 1995)
- Ab initio study of Diels-Alder reactions of cyclopentadiene with ethylene, isoprene, cyclopentadiene, acrylonitrile, and methyl vinyl ketone (Journal of the American Chemical Society, 1993)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H311: Toxic in contact with skin
Danger Acute toxicity, dermal - Category 3 - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - 1,3-cyclopentadiene
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SMILESC1C=CC=C1
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InChIKeyZSWFCLXCOIISFI-UHFFFAOYSA-N
- Pubchem - Cyclopentadiene
- Wikipedia - cyclopentadiene
Cyclopentadiene is an organic compound with the formula C5H6. This colorless liquid has a strong and unpleasant odor. At room temperature, this cyclic diene dimerizes over the course of hours to give dicyclopentadiene via a DielsAlder reaction.
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