| Weight | 156.141 g/mol |
|---|---|
| Formula | C6H8N2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,3-Dimethylbarbituric acid (769-42-6)
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- Sequential one-pot bimetallic Ir(III)/Pd(0) catalysed mono-/bis-alkylation and spirocyclisation processes of 1,3-dimethylbarbituric acid and allenes (Chemical Communications, 2006)
- Shaken Not Stirred: A Facile Synthesis of 1,4Bis(furo[2,3d]pyrimidine2,4(1H,3H)dione5yl)benzenes by OnePot Reaction of Isocyanides, N,NDimethylbarbituric Acid, and Terephthaldialdehyde. (Bioorganic & Medicinal Chemistry Letters, 2006)
- Competition between hydrogen bonding and donoracceptor interactions in co-crystals of 1,3-dimethylbarbituric acid with aromatic amines (New Journal of Chemistry, 2001)
- Electrochemical investigations of some antibacterial compounds obtained by the coupling of sulphadrugs with 1,3-dimethylbarbituric acid (Journal of Electroanalytical Chemistry, 1984)
- 5-Arylidene 1, 3-Dimethylbarbituric Acid Derivatives, Mild Organic Oxidants for Allylic and Benzylic Alcohols (Chemical & Pharmaceutical Bulletin, 1988)
- Oxidation of thiol by 5-arylidene 1,3-dimethylbarbituric acid and its application to synthesis of unsymmetrical disulfide (Tetrahedron Letters, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C(=O)CC(=O)N(C1=O)C
-
InChIKeyVVSASNKOFCZVES-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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