1) Cyclohexyl bromide
六氢溴代苯
2) Bromocyclohexane
六氢溴代苯
3) Cyclohexane, bromo-
六氢溴代苯
4) hexahydroquinoline
六氢喹啉
1.
Synthesis of 4-Aryl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate in Ionic Liquid;
在离子液体中4-芳基-5-氧代-1,4,5,6,7,8-六氢喹啉-3-羧酸酯的合成
2.
Synthesis of Methyl 2,7,7-trimethyl-5-oxo-4-aryl-1,4,5,6,7,8-hexahydroquinoline-3-carboxylateUnder Microwave Irradiation and Elucidation of Its Structure;
2,7,7-三甲基-5-氧代-4-芳基-1,4,5,6,7,8-六氢喹啉-3-羧酸甲酯的微波合成及其结构确证
3.
Synthesis of Ethyl 2,7,7-Trimethyl-5-oxo-4-aryl-1,4,5,6,7,8- hexahydroquinoline-3-carboxylate in Water;
水介质中2,7,7-三甲基-5-氧代-4-芳基-1,4,5,6,7,8-六氢喹啉-3-羧酸乙酯的合成
5) Hexahydropyridine
六氢吡啶
1.
Preparation of Supramolecular Compound α-Zirconium Phosphate-Hexahydropyridine and its Adsorption Property Against Phenols in Wastewater;
α-磷酸氢锆-六氢吡啶的超分子插层组装及其对废水中酚的吸收研究
2.
A study of the intercalation reaction of hexahydropyridine with α-zirconium hydrogen phosphate;
六氢吡啶对α-磷酸氢锆的插层研究(英文)
3.
A strong and stable room temperature phosphorescence(RTP) emission was observed from the ternary inclusion complex of α-bromonaphthalene(α-BrN)/β-cyclodextrin(β-CD)/hexahydropyridine(HHP) without deoxygenation from solution in the presence of micro amount of HHP.
微量六氢吡啶(HHP)存在下,由于三元包络物α-溴代萘(-αB rN)/β-环糊精(-βCD)/HHP的形成,不经除氧就可观察到强而稳定的室温磷光(RTP)发射。
6) hexahydropyridazine
六氢哒嗪
1.
Improving synthesis of hexahydropyridazine;
六氢哒嗪合成方法的改进
2.
This article summarized the method for the producing hexahydropyridazine.
介绍了六氢哒嗪的合成方法,并对合成路线进行了讨论。
3.
This research focused on the chemical modification of natural compound validoxylamine A and small-molecular compound hexahydropyridazine.
本论文分别对天然化合物井冈羟胺A和小分子化合物六氢哒嗪进行结构修饰,合成了一系列新化合物,并对其中部分进行了生物活性测试。
参考词条
补充资料:六氢溴代苯
分子式:C6H11Br
分子量:163.06
CAS号:108-85-0
性质:无色液体。熔点-56.5℃,沸点166.2℃,45.5℃(1.33kPa),相对密度1.3359(20/4℃),折光率1.4957。闪点62℃。与乙醇、乙醚、丙酮、苯和四氯化碳混溶,不溶于水。有刺激性气味。
制备方法:由环乙醇与溴氢酸反应而得:将环乙醇与48%氢溴酸加热回流6h。在反应混合物中加入少量水,分出下层的有机相,用无水氯化钙干燥。蒸馏,收集163-165℃馏分即为成品。产率74%。
用途:有机合成中间体。
分子量:163.06
CAS号:108-85-0
性质:无色液体。熔点-56.5℃,沸点166.2℃,45.5℃(1.33kPa),相对密度1.3359(20/4℃),折光率1.4957。闪点62℃。与乙醇、乙醚、丙酮、苯和四氯化碳混溶,不溶于水。有刺激性气味。
制备方法:由环乙醇与溴氢酸反应而得:将环乙醇与48%氢溴酸加热回流6h。在反应混合物中加入少量水,分出下层的有机相,用无水氯化钙干燥。蒸馏,收集163-165℃馏分即为成品。产率74%。
用途:有机合成中间体。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。