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17365-01-4

17365-01-4 Structure

17365-01-4 Structure
IdentificationBack Directory
[Name]

ETIROXATE
[CAS]

17365-01-4
[Synonyms]

CG-63
CG-635
ETIROXATE
DL-a-Methyl-thyroxine Ethyl Ester
DL-α-Methyl-thyroxine Ethyl Ester
O-(4-Hydroxy-3,5-diiodo-phenyl)-3,5-diiodo-α-methyl-DL-tyrosine Ethyl Ester
O-(4-Hydroxy-3,5-diiodo-phenyl)-3,5-diiodo-a-methyl-DL-tyrosine Ethyl Ester
(±)-2-Amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]-2-methylpropionic acid ethyl ester
[Molecular Formula]

C18H17I4NO4
[MDL Number]

MFCD00865750
[MOL File]

17365-01-4.mol
[Molecular Weight]

818.935
Chemical PropertiesBack Directory
[Appearance]

Tan Solid
[Melting point ]

149-1510C
[storage temp. ]

-20°C Freezer
[solubility ]

DMSO, Methanol
[form ]

Solid
[color ]

Tan
Hazard InformationBack Directory
[Chemical Properties]

Tan Solid
[Uses]

Derivative of thyroxine. Antilipemic
[Originator]

Skleronorm,Gruenenthal,W. Germany,1977
[Definition]

ChEBI: Etiroxate is an aromatic ether.
[Manufacturing Process]

7.91 g of α-methyl thyroxine are suspended in 150 cc of ethanol. While heating, the solution is saturated with dry hydrogen chloride. Thereafter, the solvent is distilled off at reduced pressure. The residue is dissolved in a mixture of ethanol and water (1:1). Adding a 5% solution of sodium hydrogen carbonate in water, the ethyl ester of α-methyl thyroxine precipitates; melting point: 156°C to 157°C after recrystallization from ethanol. The yield is 6.05 g, i.e., 74% of the theoretical yield.
[Therapeutic Function]

Antihyperlipoproteinemic
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