Weight | 100.073 g/mol |
---|---|
Formula | C4H4O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Tetronic acid (4971-56-6)
Score:
#2935 in Biochemistry
,
#7175 in Chemistry
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- 3-Alkanoyl-5-hydroxymethyl tetronic acid homologues and resistomycin : new inhibitors of HIV-1 protease. I: Fermentation, isolation and biological activity (The Journal of Antibiotics, 1994)
- Synthesis of a tetronic acid library focused on inhibitors of tyrosine and dual-specificity protein phosphatases and its evaluation regarding VHR and Cdc25B inhibition (Journal of Medicinal Chemistry, 2001)
- Tetronic Acid Biosynthesis in Molds II. FORMATION OF PENICILLIC ACID IN PENICILLIUM CYCLOPIUM (Journal of Biological Chemistry, 1962)
- Spirodiclofen and spiromesifen: Novel acaricidal and insecticidal tetronic acid derivatives with a new mode of action (Chimia, 2003)
- Toxicity and efficacy of spiromesifen, a tetronic acid insecticide, against sweetpotato whitefly (homoptera: aleyrodidae) on melons and collards (Crop Protection, 2004)
- The total synthesis of agglomerin A and ()-carolinic acid. A general method for the preparation of 3-acyl tetronic acids via direct acylation of O-methyl 3-stannyl tetronates (Tetrahedron, 1991)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(=O)COC1=O
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InChIKeyJCGNDDUYTRNOFT-UHFFFAOYSA-N
- Pubchem - Tetronic acid
- Wikipedia - tetronic acid
Tetronic acid is a chemical compound, classified as a -lactone, with the molecular formula C4H4O3. It interconverts between keto and enol tautomers: Many natural products such as ascorbic acid (vitamin C), penicillic acid, pulvinic acids, and abyssomicins possess the -keto--butyrolactone motif of tetronic acid. In organic synthesis, it is used as a precursor for other substituted and ring-fused furans and butenolides.
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