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2192-21-4

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Basic Information
CAS No.: 2192-21-4
Name: 2'-[2-(diethylamino)ethoxy]-3-phenylpropiophenone hydrochloride
Molecular Structure:
Molecular Structure of 2192-21-4 (2'-[2-(diethylamino)ethoxy]-3-phenylpropiophenone hydrochloride)
Formula: C21H27 N O2 . Cl H
Molecular Weight: 361.95
Synonyms: Propiophenone,2'-[2-(diethylamino)ethoxy]-3-phenyl-, hydrochloride (6CI,7CI,8CI); Asmedol;Baxacor; Corodilan; Dialicor; Etafenone hydrochloride; Heptaphenone;Pagano-Cor; Relicor; o-(b-Diethylaminoethoxy)phenylpropiophenone hydrochloride
Density: 1.043g/cm3
Boiling Point: 464.2°Cat760mmHg
Flash Point: 234.5°C
Safety: Poison by ingestion and intravenous routes. When heated to decomposition it emits very toxic fumes of NOx and HCl.
PSA: 29.54000
LogP: 5.02470
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Chemistry

IUPAC Name :1-[2-(2-Diethylaminoethyloxy)phenyl]-3-phenylpropan-1-one hydrochloride
Synonyms: 1-Propanone, 1-(2-(2-(diethylamino)ethoxy)phenyl)-3-phenyl-, hydrochloride (9CI) ; 1-Propanone, 1-[2-[2- (diethylamino)ethoxy]phenyl]-3-phenyl-, hydrochloride ; Etafenone hydrochloride (JAN) ; Propiophenone, 2'-[2- (diethylamino)ethoxy]-3-phenyl-, hydrochloride
CAS NO:2192-21-4
Molecular Formula of 1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride (CAS NO.2192-21-4) : C21H28ClNO2
Molecular Weight of 1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride (CAS NO.2192-21-4) : 361.90552
Molecular Structure of 1-(2-(2-(Diethylamino)ethoxy)phenyl)-3-phenyl-1-propanone hydrochloride (CAS NO.2192-21-4) :
                                                          
EINECS: 218-587-9
Flash Point: 234.5 °C
Enthalpy of Vaporization: 72.56 kJ/mol
Boiling Point: 464.2 °C at 760 mmHg
Vapour Pressure: 8.53E-09 mmHg at 25°C

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD50 oral 50mg/kg (50mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1664, 1969.
mouse LD50 intraperitoneal 90mg/kg (90mg/kg)   Drugs in Japan Vol. -, Pg. 180, 1990.
mouse LD50 intravenous 28mg/kg (28mg/kg)   Pharmaceutical Chemistry Journal Vol. 23, Pg. 966, 1989.
mouse LD50 oral 352mg/kg (352mg/kg)   Drugs in Japan Vol. 6, Pg. 109, 1982.
mouse LD50 subcutaneous 234mg/kg (234mg/kg)   Pharmaceutical Chemistry Journal Vol. 21, Pg. 646, 1987.
rat LD50 intraperitoneal 66mg/kg (66mg/kg)   Drugs in Japan Vol. -, Pg. 180, 1990.
rat LD50 intravenous 20800ug/kg (20.8mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1664, 1969.
rat LD50 oral 716mg/kg (716mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1664, 1969.
rat LD50 subcutaneous 1900mg/kg (1900mg/kg)   Drugs in Japan Vol. -, Pg. 180, 1990.

Safety Profile

Poison by ingestion and intravenous routes. When heated to decomposition it emits very toxic fumes of NOx and HCl.