| Weight | 40.065 g/mol |
|---|---|
| Formula | C3H4 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Allene
propadiene
463-49-0, 12075-35-3, 60731-10-4
Score:
#1228 in Physics
,
#3526 in Chemistry
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- A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis (Plant Journal, 2002)
- Modern allene chemistry (2004)
- Stoichiometric and catalytic hydroamination of alkynes and allene by zirconium bisamides Cp2Zr(NHR)2 (Journal of the American Chemical Society, 1992)
- Cooperative, Highly Enantioselective Phosphinothiourea Catalysis of ImineAllene [3 + 2] Cycloadditions (Journal of the American Chemical Society, 2008)
- Molecular cloning of an allene oxide synthase: a cytochrome P450 specialized for the metabolism of fatty acid hydroperoxides (Proceedings of the National Academy of Sciences of the United States of America, 1993)
- Allene oxide synthase: a major control point in Arabidopsis thaliana octadecanoid signalling (Plant Journal, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - propadiene
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SMILESC=C=C
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InChIKeyIYABWNGZIDDRAK-UHFFFAOYSA-N
- Pubchem - Allene
- Wikipedia - propadiene
Propadiene is the organic compound with the formula H2C=C=CH2. It is the simplest allene or compound with two adjacent C=C double bonds, and can also be identified as allene. As a constituent of MAPP gas, it has been used as a fuel for specialized welding.
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Allene
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