Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 69237Erstellt: 26. Oktober 2026

Ethyldibromacetat

ethyl 2,2-dibroMoacetate · Ethyl dibromoacetate · dibromo-aceticaciethylester · Dibromoacetic acid, ethyl ester · Ethyl dibromoacetate, tech., 83% · Ethyl dibromoacetate, pract., 95% · Ethyl dibromoacetate , 83%, tech. · Acetic acid, dibromo-, ethyl ester

https://huagongshe.com/de/chemical/69237

Molekülstruktur von Ethyldibromacetat

Identifikatoren & physikalische Daten

CAS No.617-33-4
SummenformelC4H6Br2O2
Durchschnittliche Molmasse245,9 g/mol
Monoisotopische Masse243,87345363 g/mol
SMILESCCOC(=O)C(Br)Br
InChIKeyNIJGVVHCUXNSLL-UHFFFAOYSA-N
PubChem CID69237
EC No.210-510-7
DTXSIDDTXSID7060673
Lokaler NameEthyldibromacetat

Chemische & physikalische Eigenschaften

XLogP2,2
Polarare Oberfläche (TPSA)26,3
H-Brücken-Donoren0
H-Brücken-Akzeptoren2
Frei drehbare Bindungen3
Schwere Atome8
Formalladung0
Komplexität82,1
SpringerMaterials PropertiesOptical coefficient
Schmelzpunkt76-78°
Siedepunkt77 °C (12 mmHg)
Dichte1.902
Brechungsindex1.492-1.502
Flammpunkt76-78°C/12mm
LagerbedingungenRT, stored under nitrogen
LöslichkeitSoluble in hexane, ether, CH2Cl2, acetone, EtOAc, ethanol.
EPA chemische InformationenAcetic acid, dibromo-, ethyl ester (617-33-4)

Sicherheit & Vorschriften

GHS-EinstufungDangerH301 (20%): Toxic if swallowed [Danger Acute toxicity, oral]P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 5 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesAcute Tox. 3 (20%)
TSCA-Inventar-StatusTSCA listed
UN-Transportnummer3265
R-Sätze (R)36/37/38
GefahrensymboleXi
Sicherheitshinweise (S)37/39-26

Anwendungen & Verwendung

Beschreibung

Ethyl dibromoacetate is used in preparation of α-bromo and α,α-dialkyl substituted esters; undergoes Reformatsky/Darzens reactions with aldehydes and ketones.

Verwenden

Ethyl dibromoacetate can be used to produce diphenoxy-acetic acid ethyl ester. It is used in organic synthesis.