Weight | 82.102 g/mol |
---|---|
Formula | C5H6O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
3-Cyclopenten-1-one (14320-37-7)
Score:
#2389 in Physics
,
#7288 in Chemistry
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- Prostaglandin synthesis via two-component coupling. Highly efficient synthesis of chiral prostaglandin intermediates 4-alkoxy-2-alkyl-2-cyclopenten-1-one and 4-alkoxy-3-alkenyl-2-methylenecyclopentan-1-one (Journal of Organic Chemistry, 1988)
- A total synthesis of racemic and optically active terrein (trans-4,5-dihydroxy-3-[(E)-1-propenyl]-2-cyclopenten-1-one). (Tetrahedron-asymmetry, 1990)
- Highly regio- and stereoselective 1,1-cycloaddition of carbon monoxide with 1,4-dilithio-1,3-dienes. Novel synthetic methods for 3-cyclopenten-1-one derivatives. (Journal of the American Chemical Society, 2001)
- Synthesis of 3-cyclopenten-1-one and 3-cyclopenten-1-ol (Journal of Organic Chemistry, 1967)
- Far-infrared spectrum and ring-puckering of 3-cyclopenten-1-one (Journal of Molecular Spectroscopy, 1974)
- Cyclization of Dicobalthexacarbonyl Complexes of Allyl Propargyl Ethers on the Surface of Chromatography Adsorbents. A Convenient Method for the Preparation of Substituted 3-Oxabicyclo[3.3.0]oct-5-en-7-one and 4-Hydroxymethyl-2-cyclopenten-1-one Derivatives from Common Precursors (Synthesis, 1989)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C=CCC1=O
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InChIKeyKQAVUGAZLAPNJY-UHFFFAOYSA-N
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Similar Compounds
2-CYCLOPENTEN-1-ONE
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(5187-71-3)
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(6140-65-4)
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(502-56-7)
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(1295-35-8)
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2,6-Dimethyl-4-heptanone
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