| Weight | 281.399 g/mol |
|---|---|
| Formula | C19H23NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
Cinnamedrine (90-86-8)
cinnamedrine hydrochloride, (S-(R*,S*))-isomer · cinnamedrine hydrochloride, ((R*,S*)-(+-))-isomer · alpha-(1-(cinnamylmethylamino)ethyl)benzyl alcohol
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cinnamedrine hydrochloride, (S-(R*,S*))-isomer
- cinnamedrine hydrochloride, ((R*,S*)-(+-))-isomer
- alpha-(1-(cinnamylmethylamino)ethyl)benzyl alcohol
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SMILESCC(C(C1=CC=CC=C1)O)N(C)CC=CC2=CC=CC=C2
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InChIKeyYMJMZFPZRVMNCH-UHFFFAOYSA-N
- Pubchem - Cinnamedrine
- Wikipedia - cinnamedrine
Cinnamedrine (INN, USAN), also known as N-cinnamylephedrine, is a sympathomimetic drug with similar effects relative to those of ephedrine. It also has some local anesthetic activity. Cinnamedrine was previously used, in combination with analgesics, as an antispasmodic to treat dysmenorrhea in the over-the-counter drug Midol in the 1980s.
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Synthesis
Reactant
+
BENZYL CHLORIDE
(Wittig)
Reactant
+
CHLOROBENZENE
(Stille)
Reactant
+
CHLOROBENZENE
(Grignard alcohol)
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