2,4-Dihydroxy-5-nitropyrimidine structure
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Common Name | 2,4-Dihydroxy-5-nitropyrimidine | ||
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CAS Number | 611-08-5 | Molecular Weight | 157.084 | |
Density | 1.9±0.1 g/cm3 | Boiling Point | 453.3±48.0 °C at 760 mmHg | |
Molecular Formula | C4H3N3O4 | Melting Point | >300 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 227.9±29.6 °C |
Use of 2,4-Dihydroxy-5-nitropyrimidine |
Name | 5-Nitrouracil |
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Synonym | More Synonyms |
Density | 1.9±0.1 g/cm3 |
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Boiling Point | 453.3±48.0 °C at 760 mmHg |
Melting Point | >300 °C(lit.) |
Molecular Formula | C4H3N3O4 |
Molecular Weight | 157.084 |
Flash Point | 227.9±29.6 °C |
Exact Mass | 157.012360 |
PSA | 111.54000 |
LogP | -1.72 |
Vapour Pressure | 0.0±1.1 mmHg at 25°C |
Index of Refraction | 1.701 |
Storage condition | -20°C Freezer |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | C: Corrosive;F: Flammable; |
Risk Phrases | R11 |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 2 |
RTECS | UV9104545 |
HS Code | 2933599090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2933599090 |
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Summary | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Phenobarbital induction and chemical synergism demonstrate the role of UDP-glucuronosyltransferases in detoxification of naphthalophos by Haemonchus contortus larvae.
Antimicrob. Agents Chemother. 58(12) , 7475-83, (2014) We used an enzyme induction approach to study the role of detoxification enzymes in the interaction of the anthelmintic compound naphthalophos with Haemonchus contortus larvae. Larvae were treated wit... |
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Inhibition of UDP-glucuronyltransferase activity in rat liver microsomes by pyrimidine derivatives.
Comp. Biochem. Physiol. C, Pharmacol. Toxicol. Endocrinol. 112(3) , 321-5, (1995) Thirty-one differently substituted pyrimidine bases were tested for their inhibitory effect on the glucuronidation of 4-nitrophenol and phenolphthalein by rat liver microsomes. 5-Nitrouracil (compound... |
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Thymidine phosphorylase inhibitors with a homophthalimide skeleton.
Biol. Pharm. Bull. 24(7) , 860-2, (2001) Several N-phenylhomophthalimide derivatives were prepared and their inhibitory activity on thymidine phosphorylase/ platelet-derived endothelial cell growth factor (TP/PD-ECGF) was assessed. Among the... |
2,4(1H,3H)-Pyrimidinedione, 5-nitro- |
5-nitropyrimidine-2,4(1H,3H)-dione |
5-NITRO-2,4-PYRIMIDINEDIOL |
5-Nitro-2,4(1H,3H)-pyrimidinedione |
5-nitro-1H-pyrimidine-2,4-dione |
5-nitropyrimidine-2,4-diol |
MFCD00006021 |
2,4-Dihydroxy-5-Nitropyrimidine |
5-Nitro-1H-pyrimidin-2,4-dion |
5-Nitropyrimidin-2,4(1H,3H)-dion |
NITROURACIL |
Uracil,5-nitro |
4(1H)-pyrimidinone, 2-hydroxy-5-nitro- |
2-Hydroxy-5-nitropyrimidin-4(1H)-one |
5-nitro-uracil |
EINECS 210-250-4 |
5-NITROURACIL extrapure |