| Weight | 126.111 g/mol |
|---|---|
| Formula | C6H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
4-Hydroxy-6-methyl-2-pyrone (675-10-5)
triacetic acid lactone
Score:
#2421 in Biochemistry
,
#6066 in Chemistry
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- Screening for enhanced triacetic acid lactone production by recombinant Escherichia coli expressing a designed triacetic acid lactone reporter. (Journal of the American Chemical Society, 2013)
- Palladium-catalyzed C-alkylations of the highly acidic and enolic triacetic acid lactone. Mechanism and stereochemistry (Journal of Organic Chemistry, 1988)
- Triacetic acid lactone as a potential biorenewable platform chemical (Green Chemistry, 2012)
- Asymmetric hydrogenation of 4-hydroxy-6-methyl-2-pyrone: Role of acid-base interactions in the mechanism of enantiodifferentiation (Journal of Catalysis, 2001)
- LVI.The lactone of triacetic acid (Journal of The Chemical Society, Transactions, 1891)
- Triacetic Acid Lactone, a Derailment Product of Fatty Acid Biosynthesis (FEBS Journal, 1969)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - triacetic acid lactone
-
SMILESCC1=CC(=CC(=O)O1)O
-
InChIKeyNSYSSMYQPLSPOD-UHFFFAOYSA-N
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