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1)  aryloxyacetyl urea
芳氧乙酰基脲
1.
Nine new N-(1H-3-carboxyl-1,2,4-triazol-5-yl)-N′-aryloxyacetyl ureas have been synthesized by the reaction of aryloxyacetyl isocyanates with 5-amino-1H-1,2,4-triazole-3-carboxylic acid.
通过 5 氨基 1,2 ,4 三唑 3 羧酸与芳氧乙酰基异氰酸酯反应 ,合成了 9个新的N ( 1H 3 羧基 1,2 ,4 三唑 5 基 ) N′ 芳氧乙酰基脲 ,用核磁共振氢谱、红外光谱和元素分析证明了目标化合物的结构 。
2.
Eleven new aryloxyacetyl ureas were synthesized by the reaction of 2-amino-1,3,4-thiodiazole with aryloxyacetyl isocynates in yields of 50.
通过2-氨基噻二唑与芳氧乙酰基异氰酸酯反应合成了11种新的N-(1,3,4-噻二唑-2-基)-N′-芳氧乙酰基脲化合物,产率为50。
2)  aryloxyacetyl thiourea
芳氧乙酰基硫脲
1.
Synthesis and biological activity of N-(5-trifluoromethyl-1,3,4-thiodiazol-2-yl]-N'-aryloxyacetyl thioureas;
N-(5-三氟甲基-1,3,4-噻二唑-2-基)-N'-芳氧乙酰基硫脲的合成及其生物活性
2.
Synthesis and biological activity of N-(5-trifluoromethyl-1,3,4-thiodiazol-2-yl]-N -aryloxyacetyl thioureas;
N-(5-三氟甲基-1,3,4-噻二唑-2-基)-N -芳氧乙酰基硫脲的合成及其生物活性
3.
Ten new aryloxyacetyl thioureas were synthesized by the reaction of 2-amino-5-(p-trifluoromethylphenyl)-1,3,4-thiodiazole with aryloxyacetyl isothiocyanates and the structures were confirmed by ~1H NMR,IR and elemental analysis.
2-氨基-5-(对三氟甲基苯基)-1,3,4-噻二唑与芳氧乙酰基异硫氰酸酯反应,合成了10种新的芳氧乙酰基硫脲。
3)  aryloxy thioacylsemicarbazide
芳氧乙酰氨基硫脲
4)  1-aryloxyacetyl-4-(2-methylaryloxyacetyl)thiosemicarbazides
1-芳氮基乙酰基-4-(2-甲基苯氧乙酰基)氨基硫脲
5)  1,4-di(aryloxyacetyl)-semicarbazides
1,4-二(芳氧基乙酰基)氨基脲
6)  aroyl urea
芳酰基脲
1.
Thirteen new aroyl ureas were synthesized by the reaction of 2-amino-5-(1o-chlorophenoxyethyl)-1,3,4-thiodiazole with aroyl isocyanates,and their structures were confirmend by IR,~(1)H NMR and elemental(analysis).
通过2-氨基-5-(1邻-氯苯氧乙基)-1,3,4噻-二唑与芳酰基异氰酸酯反应,合成了13种新的芳酰基脲。
2.
Thirteen N-(1,3,4-thiodiazol-2-y1)-N′-aroyl ureas were synthesize d by the reaction of aroyl iso-cyanates with 2-amino-1,3,4-thiodiazole i n yields of 54.
 2 氨基噻二唑与芳酰基异氰酸酯反应合成了 13种N -(1, 3, 4 噻二唑- 2基 ) N′ 的芳酰基脲,产率为54。
补充资料:1-氯甲酰基-3-乙酰基环亚乙基脲
分子式:C6H7ClN2O3
分子量:190.58
CAS号:41730-71-6

性质:密度1.528。熔点102-104°C。沸点278°C。闪点122°C。

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