| Weight | 54.092 g/mol |
|---|---|
| Formula | C4H6 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Methylenecyclopropane (6142-73-0)
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#2301 in Physics
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#7100 in Chemistry
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- Effect of 1-methylcyclopropene and methylenecyclopropane on ethylene binding and ethylene action on cut carnations (Plant Growth Regulation, 1996)
- Methylenecyclopropane rearrangement as a probe for free radical substituent effects. .sigma..bul. Values for commonly encountered conjugating and organometallic groups (Journal of Organic Chemistry, 1987)
- Stereochemistry of the methylenecyclopropane rearrangement : Feist's ester (Tetrahedron, 1970)
- Synthesis and direct observation of methylenecyclopropane (Journal of the American Chemical Society, 1984)
- Nickel-catalyzed reactions involving strained .sigma. bonds. IV. Nickel(0)-catalyzed reaction of methylenecyclopropane with olefins. Orientation and stereochemistry (Journal of the American Chemical Society, 1972)
- In Vitro Activity and Mechanism of Action of Methylenecyclopropane Analogs of Nucleosides against Herpesvirus Replication (Antimicrobial Agents and Chemotherapy, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=C1CC1
-
InChIKeyXSGHLZBESSREDT-UHFFFAOYSA-N
- Pubchem - Methylenecyclopropane
- Wikipedia - Methylenecyclopropane
Methylenecyclopropane is an organic compound with the formula (CH2)2CCH2. It is a colourless easily condensed gas that is used as a reagent in organic synthesis.
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