| Weight | 177.159 g/mol |
|---|---|
| Formula | C9H7NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
N-Methylisatoic anhydride (10328-92-4)
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- The chemistry of 2h-3,1-benzoxazine-2,4(1H)-dione (isatoic anhydride). 17 Synthesis of 2-alkyl-4-quinolone alkaloids via a one-step reaction of N-methylisatoic anhydride with methyl ketone enolates (Journal of Heterocyclic Chemistry, 1985)
- Polysaccharide labeling with N-methylisatoic anhydride: generation of ultraviolet chromophores and blue fluorophores. (Analytical Biochemistry, 2000)
- A convenient preparation of 1,4dihydro1methyl4oxo2quinolinecarboxaldehyde from Nmethylisatoic anhydride (Journal of Heterocyclic Chemistry, 1986)
- The chemistry of 2H3,1benzoxazine2,4(1H)dione (isatoic anhydride). 11. Reaction of Nmethylisatoic anhydride with 1cyanoacetylpiperidine (Journal of Heterocyclic Chemistry, 1983)
- Biotin-conjugated N-methylisatoic anhydride: a chemical tool for nucleic acid separation by selective 2-hydroxyl acylation of RNA (Chemical Communications, 2014)
- Analysis of amino acid mixtures after pre-column derivatisation by N-methylisatoic anhydride using HPLC. (Indian Journal of Biochemistry & Biophysics, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C2=CC=CC=C2C(=O)OC1=O
-
InChIKeyKJMRWDHBVCNLTQ-UHFFFAOYSA-N
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