CARBOCROMEN
- CAS NO.:804-10-4
- Empirical Formula: C20H27NO5
- Molecular Weight: 361.43
- MDL number: MFCD00868244
- EINECS: 212-356-6
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-05-04 17:34:42
What is CARBOCROMEN?
Originator
Intensain,Hoechst,Switz,1963
The Uses of CARBOCROMEN
Vasodilator (coronary).
Background
Carbocromen was marketed for use in Germany as a vasodilator, however, it has been discontinued due to the risk of arrhythmia development .
Definition
ChEBI: Carbocromen is a member of coumarins.
Manufacturing Process
18.7 g of 3β-diethylaminoethyl-4-methyl-7-hydroxy-coumarin chlorhydrate are
dissolved in 200 cc methyl ethyl ketone and 18 g anhydrous potassium
carbonate are added. The mixture is stirred for 1 hour at 70°C and then 12 g
bromoacetic acid ethyl ester are allowed to drop in. The reaction mixture is
stirred under reflux for 9 hours and then it is filtered off with suction in the
heat. The filtrate is concentrated in the vacuum to dryness and the resultant
residue is dissolved in ether. The etheric solution is washed with diluted
caustic soda solution for several times and, subsequently, dried with Glauber's
salt. By introduction of hydrochloric acid gas into the etheric solution the
reaction product is precipitated in the form of chlorhydrate. Yield: 15 g of 3β-
diethylaminoethyl-4-methylcoumarin-7-ethyl oxyacetate chlorhydrate having a
melting point of 154° to 156°C (= 63% of the theory).
The starting material is produced by reacting resorcinol with 2-(2-
diethylaminoethyl)acetic acid ethyl ester.
Therapeutic Function
Coronary vasodilator
Metabolism
Not Available
Properties of CARBOCROMEN
Melting point: | 220-222 °C |
Boiling point: | 488.6±45.0 °C(Predicted) |
Density | 1.126±0.06 g/cm3(Predicted) |
storage temp. | Refrigerator, under inert atmosphere |
solubility | Chloroform (Slightly), Methanol (Slightly), Water (Slightly) |
form | Solid |
pka | pKa 8.3 (Uncertain) |
color | Off-White |
Safety information for CARBOCROMEN
Computed Descriptors for CARBOCROMEN
New Products
6-Bromo 2-Iodo Indole Pyridine 2,4,6-Tricarboxaldehyde Fosfomycin EP impurity D Ivermectin EP Impurity B Rimegepant Impurity 3 Tubulysin I Tubulysin C (2S,4R)-4-amino-2-methyl-5-phenylpentanoic acid hydrochloride Tubulysin E 2,2-diethoxyethanethioamide 2-[[(3aR,4S,6R,6aS)-6-Aminotetrahydro-2,2-dimethyl-4H-cyclopenta-1,3-dioxol-4-yl]oxy]ethanol ethanedioate Imeglimin Hydrochloride IH (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine 2-(1-(Mercaptomethyl) cyclopropyl) acetonitrile 2-[2-[3(S)-3[2-(7-chloro-2-quinolinyl) ethenyl] phenyl-3- hydroxyl propyl] phenyl]-2-propanol Calcium Sodium Phosphosilicate IH 4-Bromo-N,N-bis(4-iodophenyl)aniline 2-Ethoxy-4-nitrobenzoic acid 4-(Azidomethyl)-3-chloropyridine 3-Morpholino-1-[4-(2-oxo-1-piperidyl)phenyl]-5,6-dihydropyridin-2(1H)-one (1-Isopropyl-1H-pyrazol-5-yl)boronic acid 3,6-Bis(4-iodophenyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione 1,3,5-Trimethyl-1,4-cyclohexadiene 4-bromo-7H-pyrrolo[2,3-d]pyrimidineRelated products of tetrahydrofuran
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