Grundinformationen
- Standard-SMILES
[N-]=[N+]=NCCO- InChIKey
BSULWPSUVMOMAN-UHFFFAOYSA-N- Summenformel
- C2H5N3O
- Durchschnittliche Molmasse
- 87,08 g/mol
- Monoisotopische Masse
- 87,04326178
Namen und Bezeichner
- Bevorzugter Name
- 2-Azidoethanol
- IUPAC
- 2-azidoethanol
- Englischer Name
- 2-Azidoethanol
- Summenformel
- C2H5N3O
- Molmasse
- 87.0806
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
1517-05-1- PubChem CID
- 123118
- DTXSID
DTXSID20164850- UNII
- D96992S9O1
- EC Number
- 808-606-4
- Nikkaji
- J80.218B
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,4
- Polarare Oberfläche (TPSA)
- 34,6 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 6
- Formalladung
- 0
- Komplexität
- 65,2
Physikochemische Eigenschaften
- Siedepunkt
- 77 ℃ · 77℃ (24 Torr)
- Dichte
- 1.146 · 1.1460
- Brechungsindex
- 1.4264 · 1.4264 (estimate)
- storage temp.
- 2 · 2-8°C, sealed storage, away from moisture
- Löslichkeit
- Chloroform (Soluble), DMSO (Sparingly), Methanol (Soluble)
- Aggregatzustand
- Oil
- Farbe
- Colourless
- Stabilität
- Light Sensitive
- InChI
- InChI=1S/C2H5N3O/c3-5-4-1-2-6/h6H,1-2H2
- InChIKey
- BSULWPSUVMOMAN-UHFFFAOYSA-N
- SMILES
- C(CO)N=[N+]=[N-]
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 38 reports by companies from 1 notifications to the ECHA C&L Inventory.
Gefahrenhinweise
Sicherheitsdaten
- ridadr
- UN2924
- hazard_class
- 3, 8
Chemie und Industrie
Anwendungen
Verwenden2-Azidoethanol is used as a reagent in the glycosylation of mono- or polysaccharides. 2-Azidoethanol is also used as a 2’-deoxy-ethynyluridine (EdU) blocker in nuclear DNA, preventing cross reactivity with other antibodies in order to better study its related pathways in the body.
Darstellung
synthetische2-Azidoethanol synthesis: Sodium azide (14.6 g, 224 mmol, 1.5 eq.) was added portion wise to a stirred mixture of 2- chloroethanol (12.0 g, 149 mmol, 1 eq.) in H2O (80 mL) at 0°C. The reaction mixture was slowly warmed up to room temperature and stirred for another 4 h. Additional sodium azide (9.71 g, 149 mmol, 1 eq.) was added and the solution was heated under reflux at 80°C overnight. After completion, the mixture was extracted with Et2O (3×50 mL) and the combined organic phases were washed with Brine (1× 10 mL) and dried over MgSO4. The solvent was removed in vacuo to yield a colorless oil (10.57 g, 121.4 mmol, 81%).1 H NMR (400 MHz, CDCl3, ppm): δ=3.77 (q, 2H, CH2 OH), 3.43 (t, 2H, CH2 N3), 2.16 (s, 1H, OH). 13C NMR (101 MHz, CDCl3, ppm): δ=61.6 (CH2 OH), 53.7 (CH2 N3). 14N NMR (CDCl3, ppm): δ= 134 (Nβ), 171 (Nγ), 319 (Nα). C2H5N3O (87.08 gmol 1 ) calcd. N 48.25, C 27.59, H 5.79%; found IS: >40 J. FS: >360 N.
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