5-Iodouracil structure
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Common Name | 5-Iodouracil | ||
---|---|---|---|---|
CAS Number | 696-07-1 | Molecular Weight | 237.983 | |
Density | 2.4±0.1 g/cm3 | Boiling Point | 401ºC | |
Molecular Formula | C4H3IN2O2 | Melting Point | 274-276 °C (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 5-iodouracil |
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Synonym | More Synonyms |
Density | 2.4±0.1 g/cm3 |
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Boiling Point | 401ºC |
Melting Point | 274-276 °C (dec.)(lit.) |
Molecular Formula | C4H3IN2O2 |
Molecular Weight | 237.983 |
Exact Mass | 237.923904 |
PSA | 66.24000 |
LogP | 0.14 |
Index of Refraction | 1.706 |
Storage condition | 0-6°C |
Water Solubility | SOLUBLE IN COLD WATER |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H302-H312-H315-H319-H332-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T:Toxic; |
Risk Phrases | R46;R20/21/22;R36/37/38 |
Safety Phrases | S53-S22-S26-S36/37/39-S45 |
RIDADR | 2811 |
WGK Germany | 3 |
RTECS | YR0525000 |
HS Code | 2933599090 |
Precursor 10 | |
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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% |
Enzymatic primer-extension with glycerol-nucleoside triphosphates on DNA templates.
PLoS ONE 4(3) , e4949, (2009) Glycerol nucleic acid (GNA) has an acyclic phosphoglycerol backbone repeat-unit, but forms stable duplexes based on Watson-Crick base-pairing. Because of its structural simplicity, GNA is of particula... |
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Highly hydrophilic and nonionic poly(2-vinyloxazoline)-grafted silica: a novel organic phase for high-selectivity hydrophilic interaction chromatography.
Anal. Bioanal. Chem 406(19) , 4585-93, (2014) A new hydrophilic and nonionic poly(2-vinyloxazoline)-grafted silica (Sil-VOX(n)) phase was synthesized and applied for the separation of nucleosides and nucleobases in hydrophilic interaction chromat... |
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Preparation and properties of oligodeoxynucleotides containing 5-iodouracil and 5-bromo- and 5-iodocytosine.
Bioconjug. Chem. 8(5) , 757-61, (1997) The behavior of oligonucleotides containing 5-iodouracil, 5-bromocytidine, and 5-iodocytidine in concentrated ammonia is described. 5-Aminouracil and 5-aminocytidine are obtained as side products when... |
5-iodopyriMidine-2.4-diol |
EINECS 211-788-2 |
5IU |
2,4(1H,3H)-Pyrimidinedione, 5-iodo- |
5-iodopyrimidine-2,4-diol |
5-Iodo-2,4(1H,3H)-pyrimidinedione |
5-IODOURACIL extrapure |
5-iodine uracil |
5-iodopyrimidine-2,4(1H,3H)-dione |
5-iodo-2,4-dioxopyrimidine |
4-iodouracil |
5-Iodpyrimidin-2,4(1H,3H)-dion |
MFCD00006020 |
5-Iodouracil |
2(1H)-pyrimidinone, 4-hydroxy-5-iodo- |
5-iodo-uraci |
5-iodo uracil |