Piperazine
英音[ pɪˈperəziːn; paɪ- ] 美音[ paɪˈperəˌzin; pɪˈperəˌzin ]

哌嗪

常用释义

词性释义

n.

[有化] 哌嗪;胡椒嗪
例句
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  • 哌嗪
通过冷冻、共沸蒸馏,从多乙烯多胺混合物中分离出哌嗪。
本文讨论了以羟胺为原料环合得到哌嗪及其衍生物。
Another way was to combine directly anhydrous piperazine with 2, 3-dichloro- bromobenzene through Ullmann reaction.
二是直接用无水哌嗪与2,3-二氯溴苯通过乌尔曼反应合成。
Piperazine citrate is the drug of choice in the treatment of Ascaris infestations .
枸橼酸哌嗪治疗蛔虫感染是最好的药物。
所述的反应溶剂为水或N-甲基哌嗪的水溶液。
Q为哌啶或哌嗪环,其可具有桥基或稠合环。
1-(2, 3-dichlorophenyl)piperazine is a kind of pharmaceutical intermediate.
1-(2,3-二氯苯基)哌嗪是一种重要的医药中间体。
Objective To study improved synthetic method of 1-[(4-chlorophenyl)phenylmethyl]-piperazine, the intermediate of cetirizine hydrochloride.
目的探讨西替利嗪的中间体1-犤(4-氯苯基)苯甲基犦-哌嗪的合成方法的改进。
二苯甲基哌嗪类化合物结构与活性的量子化学研究
哌嗪取代卟啉的合成、表征及其抗癌活性
主链含哌嗪的改性聚酰亚胺的制备和表征
吗啉环和哌嗪环类衍生物的抗血栓作用及其分子机制
Protective effect and the mechanism of action of piperazine ferulate on diabetic glomerulopathy in rats with streptozotocin-induced diabetes
阿魏酸哌嗪对糖尿病大鼠肾脏的保护作用
高效液相色谱法测人血浆中阿魏酸哌嗪浓度及其药动学研究
盐酸环丙沙星制备中哌嗪缩合的绿色合成
阿魏酸哌嗪对单侧输尿管梗阻大鼠肾间质纤维化的保护作用
芳烷醇哌嗪类化合物的合成及抗抑郁活性
乙二胺常压法合成哌嗪
紫外分光光度法快速测定哌嗪
哌嗪基改性硅乳液的合成
1·Some method about synthesis of piperazine with aliphatic amine were introduced.
介绍了由脂肪胺合成哌嗪的几种方法。
2·Objective: To establish an HPLC method to determine the plasma concentrations of buspirone hydro-chloride (BuHCl) and its active metabolite 1 - pyrimidinyl - piperazine(1 - PP).
目的:建立高效液相色谱法测定血浆中盐酸丁螺环酮及其活性代谢物1-嘧啶哌嗪浓度的方法。
3·This paper introduces the marketing situation, price trend and major production processes of piperazine at home and abroad.
介绍了哌嗪的国内外市场状况、价格走势及主要生产方法。
4·Using different concentration piperazine and IPC or TMC, through changing immersion time, heat treatment time and temperature, composite nanofiltration membrane with good performance was prepared.
用不同浓度的哌嗪水相、酰氯有机相,通过改变两相处理的时间和热处理的时间与温度寻找合适的条件制备性能较佳的平板复合纳滤膜。
5·The compounds have the connecting ring structures of piperazine or piperidine, have notable antitumor activity, and provide a new choice for preparing antitumor drugs in clinical practice.
该类化合于具有哌嗪或哌啶的连接环结构,且具有显著的抗肿瘤活性,为临床上制备抗肿瘤药物提供了新的选择。