CARBOCROMENE HYDROCHLORIDE

CARBOCROMENE HYDROCHLORIDE Suppliers list
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Products Intro: Product Name:CARBOCROMENE HYDROCHLORIDE
CAS:655-35-6
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:Chromonar hydrochloride;Antiangor;chromonar HCl;Karbokromen
CAS:655-35-6
Package:10 mg;100 mg;25 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
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Products Intro: Product Name:ChroMonar Hydrochloride
CAS:655-35-6
Package:250Mg,25Mg
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Products Intro: Product Name:ChroMonar Hydrochloride;2-[[3-[2-(DiethylaMino)ethyl]-4-Methyl-2-oxo-2H-1-benzopyran-7-yl]oxy]acetic Acid Ethyl Ester Hydrochloride; 3-(2-DiethylaMinoethyl)-4-Methyl-7-carbethoxyMethoxy -2-oxo-1,2-chroMene Hydrochloride; CarbochroMen Hydrochloride; Carboc
CAS:655-35-6
Purity:98+% Package:1Mg;5Mg;10Mg;50Mg;100Mg;500Mg
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Products Intro: Product Name:ChroMonar Hydrochloride
CAS:655-35-6

CARBOCROMENE HYDROCHLORIDE manufacturers

CARBOCROMENE HYDROCHLORIDE Basic information
Product Name:CARBOCROMENE HYDROCHLORIDE
Synonyms:CARBOCROMENE HYDROCHLORIDE;ethyl [[3-[2-(diethylamino)ethyl]-4-methyl-2-oxo-2H-1-benzopyran-7-yl]oxy]acetate hydrochloride;3-(beta-diethylaminoethyl)-4-methyl-7-(carbethoxymethoxy)-coumarin hydrochlor;antiangor;carbochromene hydrochloride;carbocromene;intensain hydrochloride;intercordin
CAS:655-35-6
MF:C20H28ClNO5
MW:397.89302
EINECS:211-511-5
Product Categories:Amines;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:655-35-6.mol
CARBOCROMENE HYDROCHLORIDE Structure
CARBOCROMENE HYDROCHLORIDE Chemical Properties
Melting point 159-160°
solubility Chloroform (Slightly), Methanol (Slightly), Water (Slightly)
form Solid
color White to Off-White
Safety Information
ToxicityLD50 in mice (g/kg): 6.3 orally; 0.528 i.p.; 0.0355 i.v. (Nitz, Potzch)
MSDS Information
CARBOCROMENE HYDROCHLORIDE Usage And Synthesis
OriginatorIntensain,Hoechst,Switz,1963
UsesVasodilator (coronary).
DefinitionChEBI: Carbocromen hydrochloride is a member of coumarins.
Manufacturing Process18.7 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 FunctionCoronary vasodilator
CARBOCROMENE HYDROCHLORIDE Preparation Products And Raw materials
Raw materialsEthyl bromoacetate
Tag:CARBOCROMENE HYDROCHLORIDE(655-35-6) Related Product Information
CHEMBRDG-BB 6149363 Cloricromenehydrochloride CARBOCROMEN (3-METHOXYPHENOXY) ACETIC ACID ETHYL ESTER 7-(CARBOXYMETHOXY)-4-METHYLCOUMARIN Cloricromene 3-[2-(DIETHYLAMINO)ETHYL]-7-HYDROXY-4-METHYLCOUMARIN HYDROCHLORIDE (4-METHYLPHENOXY) ACETIC ACID ETHYL ESTER CARBOCROMENE HYDROCHLORIDE