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| | α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride Basic information |
| Product Name: | α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride | | Synonyms: | PHENYL-2-(N-CINNAMYL-N-METHYLAMINO)PROPANOL HYDROCHLORIDE;CINNAMEDRINE HYDROCHLORIDE;CINNAMYLEPHEDRIN HYDROCHLORIDE;(±)-cinnamyl(2-hydroxy-1-methyl-2-phenylethyl)methylammonium chloride;(±)-α-[1-(Cinnamylamino)ethyl]benzyl alcohol hydrochloride;DL-Cinnamedrine hydrochloride;()-cinnamyl(2-hydroxy-1-methyl-2-phenylethyl)methylammonium chloride;α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride | | CAS: | 25441-16-1 | | MF: | C19H24ClNO | | MW: | 317.85 | | EINECS: | 246-981-0 | | Product Categories: | | | Mol File: | 25441-16-1.mol | ![α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride Structure](CAS/GIF/25441-16-1.gif) |
| | α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride Chemical Properties |
| | α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride Usage And Synthesis |
| Originator | Midol Tab,Sterling Winthrop | | Manufacturing Process | 8.0 g of 1-phenyl-2-methylaminopropanol-1 are dissolved in 30 ml of warm
benzene and the solution is mixed with 5.0 g of cinnamylbromide. It isallowed to stand for 2 h at room temperature; the whole is then filtered with
suction to eliminate the phenylmethylaminopropanol hydrobromide formed
and the filtrate is shaken out with dilute hydrochloric acid, while adding such a
quantity of water that the thick oil drops which separate are dissolved. The
aqueous extract is filtered until it is clear, rendered alkaline by means of
ammonia, shaken with ether, the ether is distilled off, the residue is
recrystalized, so 1-phenyl-2-methyl-cinnamylaminopropanol-1 was obtained.
In practice it is usually used as hydrochloride. | | Therapeutic Function | Smooth muscle relaxant |
| | α-[1-(Cinnamylmethylamino)ethyl]benzyl alcohol hydrochloride Preparation Products And Raw materials |
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