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ChemicalBook--->CAS DataBase List--->23642-66-2

23642-66-2

23642-66-2 Structure

23642-66-2 Structure
IdentificationBack Directory
[Name]

BENFLUOREX HYDROCHLORIDE
[CAS]

23642-66-2
[Synonyms]

Balans
mediator
LT00134683
Lipophoral
Einecs 245-801-8
LABOTEST-BB LT00134683
BENFLUOREX HYDROCHLORIDE
2-(alpha-Methyl-3-(trifluoromethyl)phenylethylamino)ethyl benzoat
2-((alpha-methyl-m-(trifluoromethyl)phenethyl)amino)-ethanobenzoate(est
2-((1-methyl-2-(3-(trifluoromethyl)phenyl)ethyl)amino)-ethanobenzoate(est
2-({1-[3-(Trifluoromethyl)phenyl]prop-2-yl}amino)ethyl benzoate hydrochloride
2-((1-(3-(trifluoromethyl)phenyl)propan-2-yl)amino)ethyl benzoate hydrochloride
2-[[1-Methyl-2-[3-(trifluoroMethyl)-phenyl]ethyl]aMino]ethanol Benzoate HCl Salt
2-((1-METHYL-2-[3-(TRIFLUOROMETHYL)PHENYL]ETHYL)AMINO)ETHYL BENZOATE HYDROCHLORIDE
2-[[1-METHYL-2-[3-(TRIFLUOROMETHYL)-PHENYL]ETHYL]AMINO]ETHANOL BENZOATE (ESTER) HCL
2-[[1-Methyl-2-[3-(trifluoromethyl)phenyl]ethyl]amino]ethanol benzoate hydrochloride
2-[[1-METHYL-2[3-(TRIFLUOROMETHYL)-PHENYL]ETHYL]AMINO]ETHANOL BENZOATE ESTER HYDROCHLORIDE
[EINECS(EC#)]

245-801-8
[Molecular Formula]

C19H21ClF3NO2
[MDL Number]

MFCD00058493
[MOL File]

23642-66-2.mol
[Molecular Weight]

387.82
Chemical PropertiesBack Directory
[Melting point ]

158-159?C
[storage temp. ]

Refrigerator
[solubility ]

Chlorform (Slightly), Methanol (Slightly), Water (Slightly)
[form ]

neat
[color ]

White
Safety DataBack Directory
[Hazard Codes ]

Xi
[WGK Germany ]

2
[RTECS ]

KL8275000
[Hazard Note ]

Irritant
[HS Code ]

2916399090
[Toxicity]

LD50 intraperitoneal in mouse: 108mg/kg
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Originator]

Mediator,Servier,France,1976
[Uses]

BENFLUOREX HYDROCHLORIDE can be used as an antihyperlipoproteinemic therapeutic and increase of glucose penetration and use by cells.
[Uses]

Hypolipedimic;Increase of glucose penetration and use by cells
[Manufacturing Process]

To a solution of 24.7 parts of 1-(m-trifluoromethylphenyl)-2-(β- hydroxyethyl)amino propane in 140 parts of anhydrous benzene, there were added successively 15 parts of 4.7N hydrochloric ether and a solution of 14 parts of benzoyl chloride in 24 parts of anhydrous benzene. The addition required 10 minutes, the reaction mixture was then refluxed for 8 hours.
The solid product was collected by filtration and after recrystallization from 230 parts of ethyl acetate, there were obtained 15 parts of 1-(mtrifluoromethylphenyl)- 2-(β-benzoyloxyethyl)amino propane hydrochloride melting at 161°C.
10 parts hydrochloride are put in suspension in 100 parts of water, 80 parts ether are added, then 10 parts of a concentrated solution of ammonium hydroxide. The mixture is stirred a few minutes until the salt is dissolved, then the ethered solution is poured off and dried. After the ether is eliminated, 9 parts of 1-(m-trifluoromethylphenyl)-2-(β- benzoyloxyethyl)amino propane are obtained; the base is a colorless oil.
[Therapeutic Function]

Antihyperlipidemic, Cardiovascular
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