amicarbalide

amicarbalide 구조식 이미지
카스 번호:
3459-96-9
상품명:
amicarbalide
동의어(영문):
M&B 5062 A;amicarbalide;3,3'-Diamidinocarbanilide;3,3'-Ureylenebisbenzamidine;1,3-bis(3-amidinophenyl)urea;1,3-bis(3-carbamimidoylphenyl)urea;3,3'-carbonylbis(azanediyl)dibenzimidamide;3,3'-Carbonyldiiminobis(benzenecarboxamidine);3,3'-(Carbonyldiimino)bis(benzenecarbimidamide);Benzenecarboximidamide, 3,3'-(carbonyldiimino)bis-
CBNumber:
CB9934450
분자식:
C15H16N6O
포뮬러 무게:
296.332
MOL 파일:
3459-96-9.mol

amicarbalide 속성

밀도
1.40
산도 계수 (pKa)
13.69±0.70(Predicted)

안전

amicarbalide C화학적 특성, 용도, 생산

Originator

Diampron,May and Baker

Manufacturing Process

m-Aminobenzonitrile (50 g) in anhydrous pyridine (200 ml) was treated with a solution of phosgene (15 ml) in anhydrous toluene (100 ml) over 10 min with mechanical stirring. The red solution was heated for 0.5 hour on the steam bath, cooled, and added to water (2 litres). The pale grey precipitate was filtered off, washed with ether, and crystallised from methanol (250 ml). N,N1- Di(m-cyanophenyl)urea separated as grey prisms, melting point 205-206°C.
A suspension of N,N1-di(m-cyanophenyl)urea (42 g) in anhydrous chloroform (420 ml), containing anhydrous ethanol (70 ml), was saturated with anhydrous hydrogen chloride at 0-5°C. After setting aside for 2 hours, a clear solution was obtained, which began to crystallise. After a week, the crystals were filtered off, washed well with anhydrous ether, and dried over calcium chloride. The iminoether hydrochloride so obtained (72 g) was added to saturated anhydrous ethanolic ammonia (720 ml), and the suspension heated at 55-60°C for 6 hours. After cooling to 20°C the crystals were filtered off, and recrystallized from 2 N hydrochloric add (300 ml). 3,31- Diamidinodiphenylurea dihydrochloride monohydrate separated as white prisms, melting point 286°C (decomp.).
In practice it is usually used as isethonate salt.

Therapeutic Function

Antiprotozoal

amicarbalide 준비 용품 및 원자재

원자재

준비 용품


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