탄소크롬

탄소크롬
탄소크롬 구조식 이미지
카스 번호:
804-10-4
한글명:
탄소크롬
동의어(한글):
탄소크롬
상품명:
CARBOCROMEN
동의어(영문):
D07619;Chromonar;CARBOCROMEN;carbochromen;carbochromene;Carbocromen (inn);Chromonar USP/EP/BP;CHROMONARHYDROCHLORIDE;Capolomon hydrochloride;KLOIYEQEVSIOOO-UHFFFAOYSA-N
CBNumber:
CB5771475
분자식:
C20H27NO5
포뮬러 무게:
361.43
MOL 파일:
804-10-4.mol
MSDS 파일:
SDS

탄소크롬 속성

녹는점
220-222 °C
끓는 점
488.6±45.0 °C(Predicted)
밀도
1.126±0.06 g/cm3(Predicted)
저장 조건
Refrigerator, under inert atmosphere
용해도
클로로포름(약간 용해됨), 메탄올(약간 용해됨), 물(약간 용해됨)
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
pKa 8.3 (Uncertain)
색상
회백색

안전

탄소크롬 C화학적 특성, 용도, 생산

Originator

Intensain,Hoechst,Switz,1963

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

탄소크롬 준비 용품 및 원자재

원자재

준비 용품


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