Methyl 2-(hydroxymethyl)isonicotinate

	Methyl 2-(hydroxymethyl)isonicotinate Struktur
58481-17-7
CAS-Nr.
58481-17-7
Englisch Name:
Methyl 2-(hydroxymethyl)isonicotinate
Synonyma:
Methyl 2-(hydroxyMethyl) isonicotinate;2-Hydroxymethyl-isonicotinic acid methyl ester;Methyl 2-(hydroxymethyl)pyridine-4-carboxylate;2-(hydroxymethyl)-4-Pyridinecarboxylic acid methyl ester;4-Pyridinecarboxylic acid, 2-(hydroxyMethyl)-, Methyl ester;2-(Hydroxymethyl)Isonicotinic Acid 2(HYDROXYMETHYL)4PYRIDINECARBOXYLIC ACID
CBNumber:
CB71558141
Summenformel:
C8H9NO3
Molgewicht:
167.16
MOL-Datei:
58481-17-7.mol

Methyl 2-(hydroxymethyl)isonicotinate Eigenschaften

Siedepunkt:
304.2±32.0 °C(Predicted)
Dichte
1.244±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
13.20±0.10(Predicted)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
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-Toxizität (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 Möglichkeit entfernen. Weiter spülen.

Methyl 2-(hydroxymethyl)isonicotinate Chemische Eigenschaften,Einsatz,Produktion Methoden

Synthese

The reaction was performed in 2 separate 1000 mL round-bottomed flasks. To a solution of methyl isonicotinate (70 g, 510.44 mmol) and sulfuric acid (2.340 mL, 43.90 mmol) in MeOH (700 mL) under reflux added a solution of ammonium peroxydisulfate (210 g, 918.80 mmol) in water (350 mL) over 20 min. The reaction was refluxed for 20 min and was then allowed to cool to room temperature. The solid was filtered off and washed with MeOH. After that, MeOH was removed from the filtrate under reduced pressure and then neutralized by cautious stepwise addition of solid Na2CO3 under ice-cooling. The aqueous solution was extracted with ethyl acetate and the combined organic layers were dried with Na2SO4 and evaporated. The dark-brown residue was treated with cyclohexane (3×300 mL) and the cyclohexane phase was decanted. The remaining dark-brown residue was purified by automated flash chromatography on 2 Biotage KP-SIL 340 g columns. A gradient from 25% to 100% of EtOAc in heptane over 10 CV was used as the mobile phase. Methyl 2-(hydroxymethyl)isonicotinate (27.5 g, 32%) was isolated.
	Methyl 2-(hydroxymethyl)isonicotinate

Methyl 2-(hydroxymethyl)isonicotinate Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Methyl 2-(hydroxymethyl)isonicotinate Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • 2-Hydroxymethyl-isonicotinic acid methyl ester
  • 4-Pyridinecarboxylic acid, 2-(hydroxyMethyl)-, Methyl ester
  • 2-(Hydroxymethyl)Isonicotinic Acid 2(HYDROXYMETHYL)4PYRIDINECARBOXYLIC ACID
  • Methyl 2-(hydroxyMethyl) isonicotinate
  • Methyl 2-(hydroxymethyl)pyridine-4-carboxylate
  • 2-(hydroxymethyl)-4-Pyridinecarboxylic acid methyl ester
  • 58481-17-7
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