| Identification | Back Directory | [Name]
piprozolin | [CAS]
17243-64-0 | [Synonyms]
Go 919
Go-919
W 3699
W-3699
piprozolin
piprozoline
W3699|||W-3699|||W 3699
Ethyl 2-(3-ethyl-4-oxo-5-(piperidin-1-yl)thiazolidin-2-ylidene)acetate
3-Ethyl-4-oxo-5-piperidinothiazolidin-2-ylideneacetic acid ethyl ester
Ethyl (3-ethyl-4-oxo-5-piperidin-1-yl-1,3-thiazolidin-2-ylidene)acetate
Thiazolidine,3-ethyl,4-one,5-(1-piperidyl),2-(ylidene,carbethoxymethine)
Acetic acid, [3-ethyl-4-oxo-5-(1-piperidinyl)-2-thiazolidinylidene]-, ethyl ester
Acetic acid, 2-[3-ethyl-4-oxo-5-(1-piperidinyl)-2-thiazolidinylidene]-, ethyl ester
Inchi=1/C14H22N2o3S/C1-3-16-11(10-12(17)19-4-2)20-14(13(16)18)15-8-6-5-7-9-15/H10,14H,3-9H2,1-2h | [EINECS(EC#)]
241-280-6 | [Molecular Formula]
C14H22N2O3S | [MDL Number]
MFCD01681333 | [MOL File]
17243-64-0.mol | [Molecular Weight]
298.4 |
| Hazard Information | Back Directory | [Originator]
Probilin ,Goedecke ,W. Germany ,1977 | [Uses]
Choleretic. | [Manufacturing Process]
Ethyl thioglycolate and ethyl cyanoacetate are first reacted in the presence of sodium ethylate to give 4-oxo-thiazolidin-2-ylideneacetic acid ethyl ester. That is reacted with diethyl sulfate and then with piperidine to give piprozolin. | [Brand name]
Probkin (Parke-Davis). | [Therapeutic Function]
Choleretic |
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