AMBENONIUM

AMBENONIUM 구조식 이미지
카스 번호:
7648-98-8
상품명:
AMBENONIUM
동의어(영문):
Win-8077;AMBENONIUM;[Oxalylbis(iminoethylene)]bis[(2-chlorobenzyl)diethylaminium];N,N'-[(1,2-Dioxo-1,2-ethanediyl)bis(imino-2,1-ethanediyl)]bis[2-chloro-N,N-diethylbenzenemethanaminium];(2-chlorophenyl)methyl-[2-[[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylcarbamoylformyl]amino]ethyl]-diethyl-azanium;(2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethylazaniumyl]ethylamino]-2-oxoacetyl]amino]ethyl]-diethylazanium
CBNumber:
CB41229499
분자식:
C28H42Cl2N4O2+2
포뮬러 무게:
537.57
MOL 파일:
7648-98-8.mol

AMBENONIUM 속성

안전

AMBENONIUM C화학적 특성, 용도, 생산

정의

ChEBI: A symmetrical oxalamide-based bis-quaternary ammonium ion having ethyl and 2-chlorobenzyl groups attached to the nitrogens.

상표명

Mytelase (Sanofi Aventis).

Pharmacology

The pharmacological properties of ambenonium are similar to neostigmine and pyridostigmine, and it works by reversible inactivation of cholinesterase.

Synthesis

Ambenonium, [oxalyl-bis-(iminoethylen)]-bis-[ortho-(chlorobenzyl) diethylammonium] chloride (13.2.15), is made by reacting diethyloxalate with two moles of N,N-diethylethylendiamine, forming oxalyl-bis-(iminoethylen)-bis-N,N-diethylamine (13.2.14), which is alkylated by two moles of 2-chlorobenzylchloride, giving ambenonium (13.2.15) [46¨C48].

Synthesis_7648-98-8

AMBENONIUM 준비 용품 및 원자재

원자재

준비 용품


AMBENONIUM 공급 업체

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