Weight | 196.166 g/mol |
---|---|
Formula | C7H8N4O3 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
3,7-Dimethyluric acid (13087-49-5)
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- Oxidation chemistry of 3,7-dimethyluric acid: Electrochemical and peroxidase-catalyzed mechanisms (Journal of Electroanalytical Chemistry, 1984)
- Mechanism of formation of 6-amino-5-(N-methylformylamino)-1-methyluracil and 3,7-dimethyluric acid from theobromine in the rat in vitro: involvement of cytochrome P-450 and a cellular thiol (Xenobiotica, 1990)
- Stereoelectronic effects in oxidative transformations of purines. II. Structure of 4,5-dihydro-4,5-dimethoxy-3,7-dimethyluric acid (Acta Crystallographica Section C-crystal Structure Communications, 1987)
- Stereoelectronic effects in oxidative transformations of purines. III. Structure of 4,5-ethylenedioxy-4,5-dihydro-3,7-dimethyluric acid (Acta Crystallographica Section C-crystal Structure Communications, 1987)
- Isolation and characterization of 5-[3'-(7',9'-dimethyluric acid)]-7,9-dimethyl-3,4-isouric acid: An unstable product of electrochemical oxidation of 7,9-dimethyluric acid (Journal of Electroanalytical Chemistry, 1989)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C2=C(NC1=O)N(C(=O)NC2=O)C
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InChIKeyHMLZLHKHNBLLJD-UHFFFAOYSA-N
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