| Weight | 88.106 g/mol |
|---|---|
| Formula | C4H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
3-Hydroxybutanal (107-89-1)
aldol · acetaldol · 3-hydroxybutyraldehyde
Score:
#3809 in Chemistry
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- Proline-Catalyzed Direct Asymmetric Aldol Reactions (Journal of the American Chemical Society, 2000)
- Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (Journal of the American Chemical Society, 1981)
- EnamineBased Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and DielsAlder Reactions (Accounts of Chemical Research, 2004)
- Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-Carbon Bond-Forming Reactions (Journal of the American Chemical Society, 2001)
- De Novo Computational Design of Retro-Aldol Enzymes (Science, 2008)
- Chiral bis(oxazoline) copper(II) complexes: versatile catalysts for enantioselective cycloaddition, Aldol, Michael, and carbonyl ene reactions. (Accounts of Chemical Research, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - aldol
- acetaldol
- 3-hydroxybutyraldehyde
-
SMILESCC(CC=O)O
-
InChIKeyHSJKGGMUJITCBW-UHFFFAOYSA-N
- Pubchem - 3-Hydroxybutanal
- Wikipedia - acetaldol
3-Hydroxybutanal is an aldol formerly used in medicine as a hypnotic and sedative.
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3-Hydroxybutanal
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