5-nitropyrimidine-4,6-diol structure
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Common Name | 5-nitropyrimidine-4,6-diol | ||
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CAS Number | 2164-83-2 | Molecular Weight | 157.084 | |
Density | 1.9±0.1 g/cm3 | Boiling Point | 303.5±37.0 °C at 760 mmHg | |
Molecular Formula | C4H3N3O4 | Melting Point | >300 °C(lit.) | |
MSDS | USA | Flash Point | 137.4±26.5 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 4-hydroxy-5-nitro-1H-pyrimidin-6-one |
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Synonym | More Synonyms |
Density | 1.9±0.1 g/cm3 |
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Boiling Point | 303.5±37.0 °C at 760 mmHg |
Melting Point | >300 °C(lit.) |
Molecular Formula | C4H3N3O4 |
Molecular Weight | 157.084 |
Flash Point | 137.4±26.5 °C |
Exact Mass | 157.012360 |
PSA | 112.06000 |
LogP | -0.73 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.701 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933599090 |
~72% 5-nitropyrimidi... CAS#:2164-83-2 |
Literature: Latli, Bachir; Jones, Paul-James; Krishnamurthy, Dhileepkumar; Senanayake, Chris H. Journal of Labelled Compounds and Radiopharmaceuticals, 2008 , vol. 51, # 1 p. 54 - 58 |
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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The activity of thymidine phosphorylase obtained from human uterine leiomyomas and studied in the presence of pyrimidine derivatives.
Z. Naturforsch., C, J. Biosci. 52(9-10) , 670-5, (1997) Partially purified samples of thymidine phosphorylase were obtained from four preparations of human uterine leiomyomas and uteri using the method of Yoshimura et al. (1990), Biochim. Biophys. Acta 103... |
4,6-Pyrimidinediol, 5-nitro- |
6-Hydroxy-5-nitro-4(1H)-pyrimidinone |
5-Nitro-4,6-pyrimidinediol |
EINECS 218-504-6 |
5-nitropyrimidine-4,6-diol |
5-nitro-1H-pyrimidine-4,6-dione |
MFCD00006110 |
5-Nitro-4,6-dihydroxypyrimidine |
4,6-Dihydroxy-5-nitropyriMidine |
4,6-Dihydroxy-5-nitropyrimdine |
4,6-Dihydroxy-5-nitroprimidine |