Weight | 42.037 g/mol |
---|---|
Formula | C2H2O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Ethenone (463-51-4, 12071-23-7)
ketene
Score:
#1004 in Physics
,
#2861 in Chemistry
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- Zur Kenntniss der Ketene. Diphenylketen (European Journal of Organic Chemistry, 1907)
- -Oxo ketene dithioacetals and related compounds: versatile three-carbon synthons (Tetrahedron, 1986)
- Asymmetric Synthesis of -Lactams by Staudinger Ketene-Imine Cycloaddition Reaction (European Journal of Organic Chemistry, 1999)
- Stereochemical control in the ester enolate Claisen rearrangement. 1. Stereoselectivity in silyl ketene acetal formation (Journal of Organic Chemistry, 1991)
- Ketene alkyltrialkylsilyl acetals: synthesis, pyrolysis and NMR studies (Journal of Organometallic Chemistry, 1972)
- ASYMMETRIC-SYNTHESIS OF (S)-MALIC AND (R)-MALIC ACID FROM KETENE AND CHLORAL (Journal of the American Chemical Society, 1982)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H220: Extremely flammable gas
Danger Flammable gases - Category 1 - ketene
-
SMILESC=C=O
-
InChIKeyCCGKOQOJPYTBIH-UHFFFAOYSA-N
- Pubchem - Ethenone
- Wikipedia - ketene
A ketene is an organic compound of the form RRC=C=O. Ketene also refers to CH2=C=O, occasionally called ethenone. Although they are highly useful, ketene and its various derivatives are rarely isolated.
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