2-Azidoethanol

HCID 123118CAS 1517-05-1

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

2-Azidoethanol1517-05-1CCRIS 4996UNII-D96992S9O1AZIDOETHANOL, 2-D96992S9O1DTXSID20164850RefChem:85532DTXCID20873412-azidoethan-1-olEthanol, 2-azido-Azido-PEG1
Weitere Namen anzeigen
2-Azidoethono2-Azido-1-ethanolAzidoethanolCAS_1517-05-1Azido-PEG1-alcoholEthanol,2-diazenyl-
2-azido-ethanolMFCD019405451517-14-22azidoethanol2-AzidoethanoleEMAC-PEG-EMAC,2KC2H5N3Oorb1984750

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

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

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

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

Hazard Classes and CategoriesSkin Corr. 1B (100%)

Sicherheitsdaten

ridadr
UN2924
hazard_class
3, 8

Chemie und Industrie

Anwendungen · 1 Eintrag

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 · 1 Eintrag

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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