- fenspiride
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2025-11-11
- CAS:5053-06-5
- Min. Order:
- Purity: 0.99
- Supply Ability:
- Fenspiride
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- $2500.00 / 100mg
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2025-10-27
- CAS:5053-06-5
- Min. Order:
- Purity:
- Supply Ability: 10g
- Fenspiride
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- $50.00 / 1kg
-
2023-06-28
- CAS:5053-06-5
- Min. Order: 1kg
- Purity: 99.9%
- Supply Ability: 10000MT
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| | fenspiride Basic information |
| | fenspiride Chemical Properties |
| Boiling point | 126-127 °C(Press: 2 Torr) | | density | 1.19±0.1 g/cm3(Predicted) | | pka | 12.44±0.20(Predicted) | | form | Solid:particulate/powder | | color | White to off-white | | LogP | 1.798-1.802 at 20℃ and pH6 |
| | fenspiride Usage And Synthesis |
| Originator | Viarespan,Servier,France,1969 | | Uses | Bronchodilator;anti-adrenergic (β-receptor). | | Definition | ChEBI: 8-(2-phenylethyl)-1-oxa-3,8-diazaspiro[4.5]decan-2-one is an azaspiro compound. | | Manufacturing Process | A solution of 192 g of 1-phenethyl-4-hydroxy-4-aminomethyl piperidine in 800
cc of diethylcarbonate is heated for 2? hours to reflux at about 80°C in the
presence of sodium methylate (prepared for immediate use from 2 g of
sodium). After this time, the ethyl alcohol formed during the reaction is slowly
distilled while the maximum temperature is reached. The excess ethyl
carbonate is distilled under reduced pressure. A crystallized residue is then
obtained, which is stirred with 400 cc of water and 400 cc of ether. The
solution is filtered and 125 g (77.6%) of practically pure product melting at
232°C to 233°C, are obtained.
The starting material was prepared in a yield of 58% by reduction of the
corresponding cyanohydrin. It in turn was prepared from 1-(2-phenylethyl)-4-
piperidone and potassium cyanide to give the cyanohydrin which was reduced
by lithium aluminum hydride. | | Therapeutic Function | Bronchodilator | | Pharmaceutical Applications | Fenspiride is an antagonist of 5-hydroxytryptamine, whose effect on bronchial smooth muscle expansion is between isoproterenol and theophylline. It also has the effect of unobtrusion-free respiratory tract and air resistance elimination in the lungs. It has the effect of antitussive, antipyretic, analgesic and anti-inflammatory, and the antipyretic and analgesic effect is better than aminopyrine and the anti-inflammatory effect is stronger than bute. |
| | fenspiride Preparation Products And Raw materials |
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