硝氨基

基本解释 (translations)

nitramino

与硝氨基相关的网络例句 [注：此内容来源于网络，仅供参考]

Our chief products include as follows: 5-Nitro-8-hydroxy Quinoline, 8-Aminoquinaldine, 8-Hydroxyquinoline Sulfate, 5,7-Dichloro-8-hydroxyquinaldine, 5-Nitro-0-cresol, 6-Nitro-m-cresol, 2'-Chloroacetophenone, 4-Methyl-5-thiazole ethanol, 4-Aminophenethyl alsohol.

主要产品有：硝羟喹啉，8-氨基喹啉，8-羟基喹啉硫酸盐，8-羟基喹哪啶，5，7-二氯-8-羟基喹哪啶，5-硝基邻甲酚，6-硝基间甲酚，邻氯笨乙酮，4-氨基笨乙醇，4-甲基-5-噻唑乙醇，3-羟基吡啶等。

Methods Starting from 2-chloro-4-nitrophenol and 2- pyridine hydrochlorid, 3-chloro-4-(pyridin-2-ylmethoxy) aniline was obtained via etherization and reduction. The obtained aniline coupled with N-(4-chloro-3-cyano-7-ethoxyquinolin-6-yl) acetamide to give 4-[3-chloro-4-(2-pyridylmethoxy) phenylamino]-3-cyano-7-ethoxy-6-N-acetylaminoquinoline. And then it was deacetylated, followed by reacting with4- but-2-enoyl chloride to yield the target compound neratinib.

以2-氯－4-硝基苯酚和2-氯甲基吡啶为起始原料，经醚化、硝基还原得到3-氯－4-（吡啶－2-甲氧基）苯胺，3-氯－4-（吡啶－2-甲氧基）苯胺与3-氰基－6-乙酰氨基－7-乙氧基－4-氯喹啉反应得到3-氰基－6-乙酰氨基－4-［3-氯－4-（吡啶－2-甲氧基）苯氨基］－7-乙氧基喹啉，3-氰基－6-乙酰氨基－4-［3-氯－4-（吡啶－2-甲氧基）苯氨基］－7-乙氧基喹啉去乙酰保护基后，与-4-二甲氨基－2-丁烯酰氯经酰化反应得到ner-atinib。

Odoquinazolin-4(3H)-one,7-methyl-4(3H)-quinazolinone,7-bromoquinazolin-4(3H)-one were synthesized by using anthranilic acid、2-amino-5-nitrobenzoic acid、2-amino-4-nitrobenzoic acid,6-nitro--4(3H)-quinazoline-one、o-amino-terephthalic acid, 2-amino-4-hydroxy benzoic acid、2-amino-5-bromo-benzoic acid、2-amino-5-iodine acid,1、4-butynediol、L-glutamine、isatin anhydride、formamide as starting materials and utilizing microwave-assisted synthetic approach.

本文利用微波辅助合成的方法，以邻氨基苯甲酸、2-氨基-5-硝基苯甲酸、2-氨基-4-硝基苯甲酸、邻氨基对苯二甲酸、2-氨基-4-羟基苯甲酸、2-氨基-5-溴苯甲酸、2-氨基-5-碘苯甲酸、5-甲基-2-氨基苯甲酸等为原料与甲酰胺反应，以及以1，4-丁炔二醇、L-谷氨酰胺与靛红酸酐反应，共合成了13个喹唑啉酮衍生。。。

Diamino-3,5-dinitropyridine and 2,6-diamino-3,5-dinitropyridine-1-oxide was reacted with aqueous ammonia and KMnO4 under different conditions. Substitutions in the 4 position to the nitro group were obtained with high yields: 2,4,6-triamino-3,5-dinitropyridine (81.5%) and 2,4,6-triamino-3,5-dinitropyridine-1-oxide (85.4%).

以氨水为胺化剂，KMnO4为氧化剂，在不同反应条件下实现2，6-二氨基-3，5-二硝基吡啶和2，6-二氨基-3，5-二硝基吡啶-1-氧化物4位的氧化胺化反应，目标化合物2，4，6-三氨基-3，5-二硝基吡啶和2，4，6-三氨基-3，5-二硝基吡啶-1-氧化物的收率分别达到81.5%和85.4%。

Synthesis of target compounds namely: to vanillic acid as the starting material with methanol under reflux conditions for 4 - hydroxy -3 - p-methyl, then ether, and nitration, reduction, cyclization reaction 6 - methoxy -7 - benzyloxy-quinazoline -4 - one, and then by the chloride in place of aniline, benzyloxy-off, such as etherification reaction of the target compounds; target compounds with the second and third occurrence of substitution reactions of amines by the TM1, that is, 4 - amino-benzene -6 - methoxy -7 - [2 - hydroxy -3 -(N, N-diethyl amino) oxy c] quinazoline; with ether occurred Ornidazole reaction of TM2, namely, 4 - amino-benzene -6 - methoxy -7 - [2 - hydroxy -3 -(2 - methyl -5 - nitroimidazole) C oxy] quinazoline.

本论文以嘌呤类似物喹唑啉为母核，分别在其4位和7位引入结构多样的取代苯氨基和柔性侧链，设计了一系列4-取代苯胺基-6-甲氧基-7-(2-羟基取代丙氧基)喹唑啉类化合物。目标化合物的合成即：以香草酸为起始原料，与甲醇回流条件下得到4-羟基-3-甲氧基苯甲酸甲酯，然后经过醚化、硝化、还原、环合反应得到6-甲氧基-7-苄氧基喹唑啉-4-酮，然后再经氯化、取代苯胺、脱苄氧基、醚化等反应得到目标化合物；目标化合物与二乙胺发生胺取代反应得到了TM1，即4-苯氨基-6-甲氧基-7-[2-羟基-3-丙氧基]喹唑啉；通过与奥硝唑发生醚化反应得到TM2，即4-苯氨基-6-甲氧基-7-[2-羟基-3-(2-甲基-5-硝基咪唑)丙氧基]喹唑啉。

Amino-6-methoxy Benzothiazole 99%、2-Amino Benzothiazole 99%、Veratraldehyde 99%、Veratric Acid 99%、1,2- Dimethoxy Benzene 99%、6-Nitroveratric Acid 97%、2,5-Dichlorobenzoic Acid 99%、4-Chloro-3-Nitrobenzoic Acid 99%、 3-Nitrobenzole Acid 98%、p-Methoxybenzoie Acid 99%、Anisole 99.5%、p-Methoxyacetophenonc 99%、(2'-Chloroethyl) Benzene 99%、(2'-Bromoethyl) Benzene 99%、N,N-Diethyi-m-Toiuamide 99%、Aminoacetonitrile Hydrochloride 98%、 Alkyl Diphenyl Phosphate Estrel 98%、5-Chloro-2-benzothiazolone 99%、6-bromo-2-naphthol 98%、6-Nitro-Veretric Acid Estrel 97%、4-chloro phenoxyaeetic 99

2-氨基-6-甲氧基苯骈噻唑、2-氨基苯骈噻唑、藜芦醛、藜芦酸、藜芦醚、6-硝基藜芦酸、2，5-二氯苯甲酸、3-硝基-4-氯苯甲酸、3-硝基苯甲酸、对甲氧基苯甲酸、苯甲醚、对甲氧基苯乙酮、β-氯代苯乙烷、β-溴代苯乙烷、N，N-二乙基间甲苯甲酰胺、氨基乙腈盐酸盐、磷酸二苯月桂酯、5-氯-2-苯骈噻唑酮、6-溴-2-萘酚、6-硝基藜芦酸甲酯、4-氯苯氧乙酸

For the test of such mechanism,we have measured the solubilities of n-valeric acid at 25℃in the aqueous solutions of following five cobalt ammines:(1) luteo,(2) purpuro,(3) xantho,(4) croceo and (5) flavo.

根据这样的机构，我们在25°下测了在下面五种钴络盐水溶液中正戊酸的溶度：(1)氯化六氨基钴；(2)氯化一氯五氨基钴；(3)氯化一硝基五氨基钴；(4)氯化反二硝基四氨基钴；(5)氯化顺二硝基四氨基钴。

And the conditions in cell suspension culture of Mikania micrantha were studied. The results showed that sucrose was the compatible carbon sucrose, and 30g/L sucrose concentration can satisfy the growth of Mikania micrantha cell; ammonium was absorbed under different sucrose concentration that haven't demonstrated significant specificity, and was completely absorbed on the lag phase and the early logarithmic phase; while nitrate was mainly absorbed on logarithmic phase. The density-dependent of Mikania micrantha cell starting to grow and density-inhibited of cell growth were proposed, the fittest inoculating quantity of Mikania micrantha in cell suspension culture was 40g/L.

并对微甘菊细胞悬浮培养条件进行研究，结果表明，微甘菊细胞生长适宜的碳源是蔗糖，并且较合适的蔗糖浓度为30g／L；在不同蔗糖浓度下氨基氮的吸收差别不大，氨基氮在迟滞期和对数期前期已基本消耗完毕，对数期生长主要利用硝基氮，因而提出，在微甘菊细胞液体悬浮培养中，氮源可以采用初始低氨基氮浓度，对数期中间维持高硝基氮，而且对数期中逐步流加少量的氨基氮；微甘菊细胞迟滞期分裂启动存在密度依赖现象，对数期生长存在密度抑制现象，最适接种量为40g／L。

The results of batch experiments showed that the anaerobic biodegradation kinetics of 2-CNB and 4-CNB by granular sludge were follwed by first-order reaction. The nitro groups of 2-CNB and 4-CNB were more easily attacked by electron than chlorines and they were reductively biotransformed to amino groups under anaerobic conditions. The acclimated anaerobic granular sludge, which could dechlorinate 4-chloroanline to aniline, showed that it had the ability of para-dechlorinating. The anaerobic biodegradating on pathway of 2-CNB and 4-CNB were suggested as follows:AbstractIn ZVI(zero-valent iron, Fe0)-reduction system, the nitro groups of 2-CNB and 4-CNB were reductively transformed to amino groups.

2分批试验结果证明，颗粒污泥降解2-CNB和4-CNB遵循一级动力学，在厌氧条件下，CNB发生序列的硝基还原与脱氯作用，苯环上的硝基比氯原子更容易受到亲电子攻击，发生还原反应生成氨基；所获得的颗粒污泥具有对位脱氯活性，可使4-CA进一步脱氯形成苯胺。2-CNB和4-CNB厌氧降解的建议性途径为： ZVI(Zero-valentiron)对2-CNB和4-CNB的作用主要是将苯环上的硝基还原为氨基；在ZVI与污泥共还原转化体系中，ZVI对氯代硝基苯的硝基转化具有一定的促进作用，但因ZVI对中间产物的吸附特性，终产物形成速率趋慢。

The main research work of this dissertation is as follows: Based on the chemical reaction engineering theory and the nitrobenzene electroreduction mechanism, the plate and frame electrolyzer was designed and applied to the process of electroreduction nitrobenzene to p-aminophenol. This dissertation measured the residence time distribution data of the electrolyzer by means of the pulse response method and studied the rule of flow pattern along with the current capacity change. Under different conditions ,this dissertation studied the cyclic voltammetry properties of nitrobenzene on different electrodes by means of the dynamic cyclic voltammetry method and the electrode materials applied to the NB electroreduction have been selected primarily.Baseed on the results of cyclic voltammetry tests, this dissertation used p-electrode systems to measure the steady-state- polarization curves of nitrobenzene on different electrodes in H-type diaphragm cell, and obtained each primary factor s influence rule and the exchange current density value of each electrode.And then on the basis of the conclusions of fundamental researchs upword, the effects of influence factors on the the yield of p-aminophenol and the current efficiency,such as electrode material, current density, quantity of electricity circulated, nitrobenzene concentration . sulpuric acid concentration and so on, have been studied in detail in the systems of hign temperature , strong acidity and oxygen-poorthrough a series of electrolysis experiments in this paper.After all using Pb as anode Monel metal as cathode Dupont Nafion 417 cation-exchange membrane as membrane, this dissertation obtained the optimum technological condition: reaction temperature about 85C, current density 500A m-2, sulphuric acid concentration 20%wt.

论文的主要研究工作为：运用化学反应工程理论，结合硝基苯的电还原机理，设计出用于硝基苯直接电还原合成对氨基苯酚实验的板框式电解槽，并利用脉冲响应法测定了该板框式电解槽的停留时间分布数据，研究了流型随流量变化的规律；通过动态循环伏安法研究了硝基苯在不同电极上、不同条件下的循环伏安特性，初步评选出了用于硝基苯电还原的电极材料；结合循环伏安的测定结果，在H型隔膜电解槽中采用三电极体系测定了硝基苯在不同电极上、不同条件下的稳态极化曲线，得到了各主要因素的影响规律及硝基苯在各个电极上电还原的交换电流密度数值；在基础研究结论指导下，采用板框式电解槽，在高温、强酸、贫氧系统中，进行了一系列的电解实验，分别考察了电极材料、电流密度、通电量、硝基苯浓度、硫酸浓度等因素对收率及电流效率的影响，最终选择以蒙乃尔合金电极作为阴极、铅合金为阳极、Dupont Nofion 417阳离子交换膜为隔膜，得到由硝基苯直接电还原制对氨基苯酚的最佳电解工艺条件：反应温度85℃，电流密度500A·m~(-2)，硫酸浓度20％wt。

与硝氨基相关的网络解释 [注：此内容来源于网络，仅供参考]

ACB 2：氨基-4-氯苯胺

AC 偶氮(二)碳酰胺 | ACB 2-氨基-4-氯苯胺 | ACNU 嘧啶亚硝脲

cyclic N-nitroso compound：环状N-亚硝基化台钧

cyclamate 环己氨基磺酸盐 | cyclic N-nitroso compound 环状N-亚硝基化台钧 | cyclochlorotine 环氯素

dinitrophenol：二硝基酚

其中包括氨基比林(aminopyrine)、阿斯凡纳明(arsphenamine)、二硝基酚(dinitrophenol)和磺胺剂衍生物. 乃卡巴精化合物之一(NDC)在理论上可能产生的代谢产物是对-硝基苯胺(p-nitroaniline),已知这种化合物的毒性相当高. 实验室研究,Cuckler,

dinitrophenol：二硝基酚钠

dinitrophenamicacid 二硝基氨基苯酚 | dinitrophenol 二硝基酚钠 | dinitrophenolDNP 二硝基苯酚

buyl PABA：对氨基苯甲酸丁酯

对苯二胺 p-phenylene diamine | 对氨基苯甲酸丁酯 buyl PABA | 对氨基苯酚-2-硝基苯酚 4-amino-2-nitrophenol

PAP：对氨基苯酚

论文概要:对-硝基苯酚(PNP)液相催化加氢合成对-氨基苯酚(PAP)是一条具有收率高、产品质量好、环境友好等优点的工艺路线,研制和开发高活性、高选择性的PNP加氢反应用负载型Ni基催化剂具有重要的意义.

2-amino-5-methyl thiazole：2-氨基5-甲基 唑

2-氨基-6-氯嘌呤 2-Amino-6-Chloropurine | 2-氨基5-甲基 唑 2-amino-5-methyl thiazole | 2-氨基,4-硝基苯酚 2 Amino 4 nitro phenol

Trinitrotoluene, TNT poisoning：三硝基甲苯中毒

41. 苯的氨基及硝基化合物中毒(不包括三硝基甲苯)Amino- and nitro- benzene compounds poisoning (excluding trinitrotolu... | 42. 三硝基甲苯中毒Trinitrotoluene, TNT poisoning | 43. 甲醇中毒 Methanol poisoni...

5-Amino Isophthalic acid：5-氨基间苯二甲酸

5-硝基间苯二甲酸乙酯 Monomethyl-5-Nitro Isophthalate | 5-氨基间苯二甲酸 5-Amino Isophthalic acid | 5-硝基间苯二甲酸 5-Nitroisophthalic acid

Aminophenazone Cyclamate：氨基比林环拉酸盐

aminonitrothiazole 氨硝噻唑 | aminophenazone cyclamate 氨基比林环拉酸盐 | aminophenazone 氨基比林