5-Bromuracil Produkt Beschreibung

5-Bromouracil Struktur
51-20-7
  • CAS-Nr.51-20-7
  • Bezeichnung:5-Bromuracil
  • Englisch Name:5-Bromouracil
  • Synonyma:5-Bromuracil
    5-BrUra;BROMOURACIL;5-bromo-uraci;5-BROMOURACIL;BROMOURACIL, 5-;Uracil, 5-bromo-;BUTTPARK 48\06-06;5-BroMouracil, 97+%;TIMTEC-BB SBB003643;5-Bromouracil, 98+%
  • CBNumber:CB6388195
  • Summenformel:C4H3BrN2O2
  • Molgewicht:190.98
  • MOL-Datei:51-20-7.mol
5-Bromuracil physikalisch-chemischer Eigenschaften
Sicherheit

5-Bromouracil Chemische Eigenschaften,Einsatz,Produktion Methoden

  • R-Sätze Betriebsanweisung: R22:Gesundheitsschädlich beim Verschlucken.
    R46:Kann vererbbare Schäden verursachen.
  • S-Sätze Betriebsanweisung: S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
    S53:Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.
    S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
  • Chemische Eigenschaften Prisms from H 2 O.
  • Verwenden A major chemical mutagen. Incorporates into DNA, altering base-pair sequencing by replacing thymine
  • Definition ChEBI: A pyrimidine having keto groups at the 2- and 4-positions and a bromo group at the 5-position.
  • Allgemeine Beschreibung White powder.
  • Air & Water Reaktionen Insoluble in water.
  • Reaktivität anzeigen A halogenated amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
  • Hazard Moderately toxic, alters DNA by replacing thymine.
  • Health Hazard ACUTE/CHRONIC HAZARDS: When heated to decomposition 5-Bromouracil emits very toxic fumes of bromide ion and NOx.
  • Brandgefahr Flash point data for 5-Bromouracil are not available, but 5-Bromouracil is probably combustible.
  • Sicherheitsprofil Moderately toxic by intraperitoneal route. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits very toxic fumes of Brand NOx.
5-Bromouracil Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
5-Bromuracil Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
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51-20-7, 5-Bromouracil Verwandte Suche:
  • 5-BROMO-PYRIMIDIN-2,4-DIOL
  • 5-BROMOURACIL (5-BROMO-2,4-DIHYDROXYPYRIMIDINE)
  • 5-BROMOURACIL extrapure
  • 5-Bromo-2,4-pyrimidinedione
  • 5-Bromo-1,2,3,4-tetrahydropyrimidine-2,4-dione
  • 5-BrUra
  • Uracil, 5-bromo- (VAN 8CI)
  • 5-Bromo-1,3-diazine-2,4-diol, 5-Bromo-2,4-dihydroxypyrimidine
  • 5-BroMouracil, 97+%
  • 3h)-pyrimidinedione,5-bromo-4(1h
  • 4(1H,3H)-Pyrimidinedione,5-bromo-2
  • 5-bromo-uraci
  • Uracil, 5-bromo-
  • 5-bromopyrimidine-2,4(1H,3H)-dione
  • 5-Bromouracil, 98+%
  • 2,4-Dihydroxy-5-bromopyrimidine
  • 5-Brom-2,4-dioxo-tetrahydropyrimidin
  • BROMOURACIL
  • BROMOURACIL, 5-
  • BUTTPARK 48\06-06
  • 5-BROMO-2,4-DIHYDROXYPYRIMIDINE
  • 5-BROMO-2,3-DIHYDROXYPYRIMIDINE
  • 5-BROMO-2,4-(1H,3H)-PYRIMIDINEDIONE
  • 5-BROMO-1H-PYRIMIDINE-2,4-DIONE
  • 5-BROMOPYRIMIDINE-2,4-DIOL
  • 5-BROMOURACIL
  • SPECS AC-907/25014019
  • TIMTEC-BB SBB003643
  • 2,4(1H,3H)-Pyrimidinedione, 5-bromo-
  • 2,4(1H,3H)-Pyrimidinedione,5-bromo-
  • 2,4-Pyrimidinedione, 1,2,3,4-tetrahydro-5-bromo
  • 51-20-7
  • C4H3N2O2Br
  • AMINE
  • Building Blocks
  • Biochemicals and Reagents
  • BioChemical
  • Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Pyrimidines
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides
  • Pyrimidine series
  • Detergents
  • Biochemistry
  • Nucleobases and their analogs
  • Nucleosides, Nucleotides & Related Reagents
  • Nucleic acids
  • Bases & Related Reagents
  • Mutagenesis Research Chemicals
  • Nucleotides
  • -