| Weight | 72.107 g/mol |
|---|---|
| Formula | C4H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
ISOBUTYRALDEHYDE (78-84-2)
isobutanal · isobutylaldehyde · 2-methylpropanal
Score:
#574 in Physics
,
#1668 in Chemistry
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- Direct photosynthetic recycling of carbon dioxide to isobutyraldehyde (Nature Biotechnology, 2009)
- Peroxidase-catalyzed formation of triplet acetone and chemiluminescence from isobutyraldehyde and molecular oxygen. (Journal of Biological Chemistry, 1985)
- Primary amino acid lithium salt as a catalyst for asymmetric Michael addition of isobutyraldehyde with -nitroalkenes (Chemical Communications, 2008)
- Chiral primary amine thiourea promoted highly enantioselective Michael reactions of isobutylaldehyde with maleimides (Tetrahedron, 2010)
- Enzyme-generated electronically excited carbonyl compounds, Acetone phosphorescence during the peroxidase-catalyzed aerobic oxidation of isobutanal. (Journal of Biological Chemistry, 1978)
- Reactions of Cyclohexylisonitrile and Isobutyraldehyde with Various Nucleophiles and Catalysts (Journal of Organic Chemistry, 1963)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H335: May cause respiratory irritation
Warning Specific target organ toxicity, single exposure; Respiratory tract irritation - Category 3 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 - isobutanal
- isobutylaldehyde
- 2-methylpropanal
-
SMILESCC(C)C=O
-
InChIKeyAMIMRNSIRUDHCM-UHFFFAOYSA-N
- Pubchem - ISOBUTYRALDEHYDE
- Wikipedia - isobutyraldehyde
Isobutyraldehyde is the chemical compound with the formula (CH3)2CHCHO. It is an aldehyde, isomeric with n-butyraldehyde (butanal). Isobutyraldehyde is manufactured, often as a side-product, by the hydroformylation of propene.
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ISOBUTYRALDEHYDE
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