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5-Methoxyuridin

5-METHOXYURIDINE Struktur
35542-01-9
CAS-Nr.
35542-01-9
Bezeichnung:
5-Methoxyuridin
Englisch Name:
5-METHOXYURIDINE
Synonyma:
1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methoxypyrimidine-2,4(1H,3H)-dione;mo(5)U;5-METHOXYURIDINE;5-MethoxyuridineA;Uridine, 5-methoxy-;5 –Methoxyuridine,RNA anticodon nucleoside for RNA vaccines and geno mics,P2Y6 receptor agonist;1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methoxy-1,2,3,4-tetrahydropyrimidine-2,4-dione
CBNumber:
CB4144845
Summenformel:
C10H14N2O7
Molgewicht:
274.23
MOL-Datei:
35542-01-9.mol

5-Methoxyuridin Eigenschaften

Dichte
1.65±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
pka
8?+-.0.10(Predicted)
Aggregatzustand
Solid
Farbe
White to off-white
maximale Wellenl?nge (λmax)
279 (pH 2);277 (pH 12)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
WGK Germany  3
HS Code  29349990
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

5-Methoxyuridin Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Solid

Verwenden

5-Methoxyuridine is an analog of Uridine (U829910) and is used as a reagent in the synthesis of 5-OMe-UDP, a potent and selective P2Y6-receptor agonist.

Definition

ChEBI: A derivative of uridine, bearing an additional methoxy substituent at position 5 on the uracil ring.

Synthese

5-Hydroxyuridine was synthesized by the method described by T. Ueda. 5-Hydroxyuridine (30 mg) was further methylated by 20 y1 of dimethyl sulfate in 0.6 ml of 0.1 N NaOH. A reaction mixture was chromatographed on Whatman 3MM paper using solvent D. The band containing 5-Hydroxyuridine was extracted with water and the extract was further purified by paper chromatography in sol vent E. These procedures gave a 25% yield of mo5l). In addition to 5-Hydroxyuridine and the raw material, the methylated products contained 5% of 5-hydroxy-3-methyl uridine and 4% of 5-methoxy-3-methyluridine.

5-Methoxyuridin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


5-Methoxyuridin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 81)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Henan Fengda Chemical Co., Ltd
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Shenzhen Nexconn Pharmatechs Ltd
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TargetMol Chemicals Inc.

support@targetmol.com United States 38631 58
PANNACEAN(HENAN)MEDICINE SCIENCE TECHNOLOGIES LTD
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haifeng.zhang@pannacean.com China 645 58

35542-01-9(5-Methoxyuridin)Verwandte Suche:


  • 5-METHOXYURIDINE
  • mo(5)U
  • Uridine, 5-methoxy-
  • 5 –Methoxyuridine,RNA anticodon nucleoside for RNA vaccines and geno mics,P2Y6 receptor agonist
  • 1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methoxypyrimidine-2,4(1H,3H)-dione
  • 5-MethoxyuridineA
  • 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methoxy-1,2,3,4-tetrahydropyrimidine-2,4-dione
  • 35542-01-9
  • C10H14N2O7
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides
  • Biochemicals and Reagents
  • BioChemical
  • Biochemicals and Reagents
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides
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