니푸르자이드

니푸르자이드
니푸르자이드 구조식 이미지
카스 번호:
39978-42-2
한글명:
니푸르자이드
동의어(한글):
니푸르자이드
상품명:
nifurzide
동의어(영문):
nifurzide;Ricridene;N'-[3-(5-Nitro-2-furyl)-2-propenylidene]-5-nitro-2-thiophenecarbohydrazide;5-Nitro-2-thiophenecarboxylic acid N'-[3-(5-nitro-2-furyl)-2-propenylidene] hydrazide;2-Thiophenecarboxylic acid, 5-nitro-, 2-[3-(5-nitro-2-furanyl)-2-propen-1-ylidene]hydrazide
CBNumber:
CB2901022
분자식:
C12H8N4O6S
포뮬러 무게:
336.28
MOL 파일:
39978-42-2.mol

니푸르자이드 속성

녹는점
235-236°
밀도
1.62±0.1 g/cm3(Predicted)
산도 계수 (pKa)
10.31±0.46(Predicted)

안전

독성 LD50 orally in mice: 3200 mg/kg (Szarvasi, Fontaine, 1972)

니푸르자이드 C화학적 특성, 용도, 생산

Originator

Ricridene,Anphar,Switz.,1981

Manufacturing Process

(a) Ethyl-5-nitro-2-thiophene carboxylate:
17.4 g (mol/10 = 17.31 g) of 5-nitrothiophene carboxylic acid are dissolved in 85 ml of absolute ethanol. A stream of gaseous hydrochloric acid is caused to enter the boiling solution to the point of saturation, and for 5 hours. Evaporation to dryness takes place and then the solid residue is washed with a sodium bicarbonate solution. It is suction-filtered and washed with water. After drying, there are obtained 17.7 g of a yellow product with a melting point of 63°C to 65°C and the yield is 88% (theoretical yield = 88%).
The N'-(5'-nitro-2'-thenoyl)hydrazide is prepared by reacting hydrazine with ethyl 5-nitro-2-thiophene carboxylate.
(b) 6.3 g (mol/30 = 6.5 g) of N1-[5'-nitro-2'-thenoyl]hydrazide are dissolved in 100 ml of dry tetrahydrofuran. 5.6 g (mol/30 = 5.55 g) of 5-nitro-2-furyl acrolein in 56 ml of tetrahydrofuran are added. Heating under reflux takes place for 1 hour and, 25 minutes after starting the heating, the crystallization commences; the crystals are suction-filtered, washed with ether and dried. There are obtained 7.9 g (yield 70%-theoretical yield = 11.2 g) of a yellow solid of melting point 235°C to 236°C.
Recrystallization (tepid dimethylformamide + ether) leaves the melting point unchanged.

Therapeutic Function

Antibacterial, Antidiarrheal

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