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1)  6-fluoro-2-pyrimindinyloxy-N-substituted phenyl benzylamine
6-氟-2-嘧啶氧基苄胺
2)  2-pyrimidinyloxy-N-arylbenzylamine
2-嘧啶氧基-N-芳基苄胺
1.
Studies of gas phase reactions of 2-pyrimidinyloxy-N-arylbenzylamine derivatives by tandem mass spectrometry;
串联质谱法研究2-嘧啶氧基-N-芳基苄胺类衍生物的气相化学反应
2.
A novel compound,a derivative of 2-pyrimidinyloxy-N-arylbenzylamine was designed and synthesized by using 2,5-dichloroaniline,6-chloro-salicylic aldehyde and 4,6-dimethoxy-2-methyl sulfonyl pyrimidine.
以2,5-二氯苯胺、6-氯水杨醛和4,6-二甲氧基-2-甲砜基嘧啶为原料,设计并合成了2-嘧啶氧基-N-芳基苄胺类化合物N-(2,5-二氯苯基)-6-氯-2-(4,6-二甲氧基-2-嘧啶氧基)苄胺,其化学结构经核磁共振氢谱和质谱分析确证。
3)  5-Fluoro-2-methoxy-4-pyrimidinamine
5-氟-2-甲氧基-4-嘧啶胺
4)  2-oxy-6-aminopyrimidine
2-氧-6-氨基嘧啶
5)  pyrimidinyloxybenzylamine
嘧啶氧苄胺
1.
The paper introduced 3 methods to synthesis 3 types of pyrimidinyloxybenzylamine compounds,and the key intermediate of 4,6-dimethyloxy-2-(methylsulfonyl)-1,3-pyrimidine were also reviewed.
嘧啶氧苄胺类化合物作为新型ALS抑制剂类除草剂,具有广谱、高效、低毒、低残留、高选择性和与环境良好的兼容性等特点。
6)  2-(4,6-dimethoxy-pyrimidin-2-yloxy)-N-het/aryl-benzylamine derivatives
2-嘧啶氧基-N-芳基苄胺类化合物
1.
According to the result of biological experiments,2-(4,6-dimethoxy-pyrimidin-2-yloxy)-N-het/aryl-benzylamine derivatives were found to have the inhibiting activity of acetolactate synthase(ALS),and the relationship between these compounds and their activity was studied by 3D-QSAR:CoMFA and CoM-SIA.
生物活性测试结果表明,2-嘧啶氧基-N-芳基苄胺类化合物对ALS具有一定的抑制活性。
补充资料:甲氧苄氨嘧啶
分子式:C14H18N4O3
分子量:290.32
CAS号:738-70-5

性质:白色或类白色结晶性粉。熔点199-203℃,25℃的溶解度(g/100ml):DMA13.86,苄醇7.29,氯仿1.82,甲醇1.21,水0.04,醚0.003,苯0.002。无臭,味苦。

制备方法:三甲氧基苯甲醛经缩合、环合而得。

用途:新型口服广谱抗菌药物。抗菌谱与磺胺药物相似而效力较强,对多种革兰氏阳性和阴性细菌有效。由于细菌对本品将易产生耐药性,故不宜单独作为抗菌药使用。甲氧苄啶与磺胺药合用可使抗菌作用增强数倍至数十倍。该品主要作磺安类药的增效药。一般按1:5的比例使用。也可作为兽药,治疗禽率大肠肝菌引起的败血症,鸡白痢,禽伤寒,霍乱,呼吸系统继发性细菌感染等。还可用于球虫病的治疗。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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