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HCID 4356513Erstellt: 23. Oktober 2026

Ethyl 2-(2-Amino-4-thiazolyl)-2-oxoacetate

EAOA · CEFA-006 · )-2-oxoacetate · 2-(2-Amino-4-thiazoL · Ethyl-2-(2-AMinothiazol-4-yl)- · Ethyl Aminothiazole Glyoxylate · Ethyl 2-amino-4-thiazoleglyoxylate · Ethyl 2-amino-α-oxo-4-thiazoleacetate

https://huagongshe.com/de/chemical/4356513

Molekülstruktur von Ethyl 2-(2-Amino-4-thiazolyl)-2-oxoacetate

Identifikatoren & physikalische Daten

CAS No.64987-08-2
SummenformelC7H8N2O3S
Durchschnittliche Molmasse200,22 g/mol
Monoisotopische Masse200,02556312 g/mol
SMILESCCOC(=O)C(=O)c1csc(N)n1
InChIKeyXNVRKLCQBZTGNA-UHFFFAOYSA-N
PubChem CID4356513
EC No.682-387-1
DTXSIDDTXSID00402308

Chemische & physikalische Eigenschaften

XLogP1
Polarare Oberfläche (TPSA)111
H-Brücken-Donoren1
H-Brücken-Akzeptoren6
Frei drehbare Bindungen4
Schwere Atome13
Formalladung0
Komplexität222
Schmelzpunkt150-152 °C(lit.)
Siedepunkt361.6±15.0 °C(Predicted)
Dichte1.405±0.06 g/cm3(Predicted)
Lagerbedingungenunder inert gas (nitrogen or Argon) at 2–8 °C
LöslichkeitDMSO (Slightly), Methanol (Slightly)
AggregatzustandSolid
pKa (Säurekonstante)1.35±0.10(Predicted)
FarbeLight Yellow to Yellow
InChIInChI=1S/C7H8N2O3S/c1-2-12-6(11)5(10)4-3-13-7(8)9-4/h3H,2H2,1H3,(H2,8,9)
InChIKeyXNVRKLCQBZTGNA-UHFFFAOYSA-N
SMILESC1(N=C(N)SC=1)C(=O)C(=O)OCC
CAS Datenbank64987-08-2(CAS DataBase Reference)

Sicherheit & Vorschriften

GHS-EinstufungWarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
Zollcode2934100090
R-Sätze (R)36/37/38
GefahrensymboleXi
Sicherheitshinweise (S)26-37/39

Anwendungen & Verwendung

Verwenden

Ethyl 2-(2-Aminothiazol-4-yl)glyoxylate is used in the synthesis of antibacterial compounds. Also used in the synthesis of antiallergic and antiinflammatory agents, as glycolic amide derivatives.