1H-Imidazole-1-sulfonyl azide hydrochloride

1H-Imidazole-1-sulfonyl azide hydrochloride Struktur
952234-36-5
CAS-Nr.
952234-36-5
Englisch Name:
1H-Imidazole-1-sulfonyl azide hydrochloride
Synonyma:
1H-Imidazole-1-sulfonyl azide hydrochloride;Imidazole-1-sulfonyl azide HCl;Imidazole-1-sulfonyl azide, HCl salt;Imidazole-1-sulfonyl azide hydrochloride;1H-Imidazole-1-sulphonylazidehydrochloride;N-diazoimidazole-1-sulfonamide hydrochloride;1H-Imidazole-1-sulfonyl Azide Hydrochloride Salt
CBNumber:
CB52547096
Summenformel:
C3H3N5O2S.HCl
Molgewicht:
210
MOL-Datei:
952234-36-5.mol

1H-Imidazole-1-sulfonyl azide hydrochloride Eigenschaften

Schmelzpunkt:
102-104℃
storage temp. 
2-8°C
Löslichkeit
Methanol (Slightly), Water (Slightly)
Aggregatzustand
Solid
Farbe
White to Off-White
Stabilität:
Hygroscopic, forms hydrazoic acid on prolonged storage and on contact with water
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
HS Code  2933299090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H242 Erwärmung kann Brand verursachen. Organische Peroxide Typen C & D Achtung
Warnung
GHS hazard pictogramssrc="/GHS02.jpg" width="20" height="20" /> P210, P220, P234, P280, P370+P378,P403+P235, P411, P420, P501
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P234 Nur im Originalbehälter aufbewahren.
P235 Kühl halten
P240 Behälter und zu befüllende Anlage erden.
P370+P378 Bei Brand: zum Löschen verwenden.
P403 An einem gut belüfteten Ort aufbewahren.

1H-Imidazole-1-sulfonyl azide hydrochloride Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

1H-Imidazole-1-sulfonyl azide hydrochloride is an azide salt, which can be used as an intermediate in organic synthesis and material chemistry, and is commonly used as a diazotropic transfer reagent in the field of chemical synthesis. It is also used in the synthesis of bioactive molecules and organic functional materials.

Synthese

1H-Imidazole-1-sulfonyl azide hydrochloride was synthesised by a series of chemical reactions using 1H-imidazole as raw material, and the specific reflective steps are as follows:
Sulfurylchloride (16.2 mL, 0.2 mol) was added dropwise to an ice-cooled suspension ofNaN3 (13.0 g, 0.2 mol) in anhydrous acetonitrile (200 mL) and themixture was stirred overnight. Imidazole (27.2 g, 0.4 mol) was addedportionwise to the ice-cooled mixture and the slurry was stirred for 5 h. Themixture was diluted by EA (400 mL) and 400 mL of water was added. The organiclayer was washed by water (2x400 mL), followed by saturated NaHCO3solution (2x400 mL) and brine (400 mL). The organic layer was dried over Na2SO4.Asolution of HCl/EtOH, obtained by dropwise addition of AcCl (21.3 mL, 0.3 mol)to ice-cooled dry ethanol (75 mL) was added dropwise to the filtrate withstirring, which was dried to get the white solid (36 g, 96% yield), which waskept desiccator under N2 atmosphere.LC-MS(ESI): [M+1]+ = 173.80, tR = 2.73 min.1H NMR (400 MHz, D2O) δ 9.43 (s, 1H), 8.00 (s, 1H), 7.60 (s, 1H).13C NMR (101 MHz, D2O) δ 137.66, 123.01, 120.20.
1H-Imidazole-1-sulfonyl azide hydrochloride synthesis

1H-Imidazole-1-sulfonyl azide hydrochloride Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


1H-Imidazole-1-sulfonyl azide hydrochloride Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • Imidazole-1-sulfonyl azide hydrochloride
  • 1H-Imidazole-1-sulphonylazidehydrochloride
  • Imidazole-1-sulfonyl azide HCl
  • 1H-Imidazole-1-sulfonyl Azide Hydrochloride Salt
  • Imidazole-1-sulfonyl azide, HCl salt
  • N-diazoimidazole-1-sulfonamide hydrochloride
  • 1H-Imidazole-1-sulfonyl azide hydrochloride
  • 952234-36-5
  • 952234-36-6
  • C3H3N5O2SHCl
  • C3H3N5O2SClH
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