| Identification | Back Directory | [Name]
oxprenolol | [CAS]
6452-71-7 | [Synonyms]
Coretal
Aids001596
Aids-001596
Oxprenolol-d7
dl-Oxprenolol
Coretal (hydrochloride)
6452-73-9 (Hydrochloride)
1-(2-allyloxyphenoxy)-3-isopropylaminopropan-2-ol
1-(2-Allyloxyphenoxy)-3-(isopropylamino)-2-propanol
1-[o-(Allyloxy)phenoxy]-3-(isopropylamino)-2-propanol
1-[2-(Allyloxy)phenoxy]-3-(isopropylamino)-2-propanol
1-(Isopropylamino)-3-[2-(2-propenyloxy)phenoxy]-2-propanol
1-(Isopropylamino)-2-hydroxy-3-[o-(allyloxy)phenoxy]propane
2-Propanol, 1-(1-methylethyl)amino-3-2-(2-propenyloxy)phenoxy-
2-Propanol, 1-[o-(allyloxy)phenoxy]-3-(isopropylamino)- (7CI, 8CI)
2-Propanol, 1-[(1-methylethyl)amino]-3-[2-(2-propenyloxy)phenoxy]- (9CI) | [EINECS(EC#)]
229-257-9 | [Molecular Formula]
C15H23NO3 | [MDL Number]
MFCD00243001 | [MOL File]
6452-71-7.mol | [Molecular Weight]
265.348 |
| Chemical Properties | Back Directory | [Melting point ]
78-80° | [Boiling point ]
408.57°C (rough estimate) | [density ]
1.0479 (rough estimate) | [refractive index ]
1.5000 (estimate) | [Contact allergens]
The beta-blocker oxprenolol induced contact dermatitis
in a worker at a pharmaceutical plant, in a division
for drug synthesis. Epichlorhydrin was also used for
the production of drugs propranolol and oxprenolol. |
| Hazard Information | Back Directory | [Description]
Oxprenolol induced contact dermatitis in a worker at a
pharmaceutical plant, in the division for drug synthesis.
Epichlorhydrin was also used for the production of
both propranolol and oxprenolol. | [Originator]
Trasicor,Ciba Geigy ,Italy,1970 | [Uses]
Oxprenolol is a free base of Oxprenolol Hydrochloride(O870500) which is a β-Adrenergic blocker. Antihypertensive, antianginal, antiarrhythmic. | [Uses]
Vasodilator(coronary). | [Definition]
ChEBI: 1-(propan-2-ylamino)-3-(2-prop-2-enoxyphenoxy)-2-propanol is an aromatic ether. | [Manufacturing Process]
75 grams of pyrocatechol monoallyl ether, 75 grams of epichlorohydrin, 75 grams of potassium carbonate and 400 ml of acetone are stirred and heated at the boil for 12 hours. The potassium carbonate is then filtered off. The solvent is distilled off in a water-jet vacuum. The residual oil is dissolved in ether and agitated with 2 N sodium hydroxide solution. The ether is separated, dried and distilled off. The residue is distilled in a water-jet vacuum. 3-(ortho-allyloxy-phenoxy)-1,2-epoxypropane passes over at 145° to 157°C under 11 mm Hg pressure. A solution of 15 grams of 3-(ortho-allyloxyphenoxy)-1,2-epoxypropane and 15 grams of isopropylamine in 20 ml of ethanol is refluxed for 4 hours. The excess amine and the alcohol are then distilled off under vacuum, to leave 1-isopropylamino-2-hydroxy-3-(orthoallyloxy-phenoxy)-propane which melts at 75° to 80°C after recrystallization from hexane.
| [Brand name]
Trasicor (Novartis). | [Therapeutic Function]
Antiarrhythmic |
|
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