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酸亚胺

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A compound derived from ammonia and containing the bivalent NH group combined with a bivalent nonacid group.

亚胺源自氨的一种化合物,含有与一个二价非酸基结合的氨基

The kinetic parameters of vanadium catalytic oxidation of azomethine H by bromate have been determined by using spectrophotometric method .

以酸性介质中痕量钒催化溴酸钾氧化甲亚胺 H显色反应为对象,利用光度法研究了反应的动力学参数。

A novel bismaleimide-modified cyanate ester was prepared to improve heat resistant,mechanical property and molding process of this type of resin.

制备了一种新型的双马来酰亚胺改性氰酸酯树脂以提高这类树脂的耐热性,力学性能及成型工艺性。

The result indicated that deoxidizing emeraldine destroyed of quinone diamide conjugate structure, both of the conductivity and solubility were reduced. The charge was delocalized along the molecular chains after protonic acid doped, which was beneficial to the electric conductivity.

结果表明,还原本征态聚苯胺破坏了聚苯胺链中的醌二亚胺的共轭结构,电导率和溶解性能均下降;质子酸掺杂本征态聚苯胺后分子链上的电荷离域程度增加,有利于电子流动,从而提高其电导率。

Methods Activate GAMP with cyanogens bromide and prepare GAMP-protein conjugates using ADH as a linker and EDAC as a coupling agent.

方法采用溴化氰活化多糖,以无水己二酸二肼为连接剂,1-乙基-1-3-(3-二甲基氨基-丙基)-碳化二亚胺为偶联剂,制备结合物并免疫小鼠,检测小鼠血清中抗GAMP与抗载体蛋白抗体及抗GAMP抗体的杀菌活性。

Methods Activate GAMP with cyanogens bromide and prepare GAMP-protein conjugates using ADH as a linker and EDAC as a coupling agent. Immunize mice with the conjugates and determine the antibodies against GAMP and carrier proteins in their sera as well as the bactericidal activity of antibody against GAMP.

采用溴化氰活化多糖,以无水己二酸二肼为连接剂,1-乙基-1-3-(3-二甲基氨基-丙基)-碳化二亚胺为偶联剂,制备结合物并免疫小鼠,检测小鼠血清中抗GAMP与抗载体蛋白抗体及抗GAMP抗体的杀菌活性。

Starting with two reactive methylene compounds, ethyl cyanoacetate and malononitrile, two 5-amino-1H-pyrazoles were prepared through the intermediates ketene dithioacetal.

从两个活泼亚甲基化合物开始,经过乙烯酮二硫代缩醛中间体,合成了两个5-氨基-1H-吡唑,以这个两个化合物为中间体,与芳香族和脂肪族α-溴代酮反应,而后经酸催化亚胺化互变异构后得到含咪唑并[1,2-b]吡唑甲硫醚类化合物6a-6g。

Tetrachloroterephthalic acid was prepared by chlorinating terephthalic acid, oleumsolvent and iodine catalyst. Tetrachloroterephthalic acid was acylated by sulphurous oxychloride in the presence of DMF to form tetrachloroterephthaloyl chloride. The acyl chloride product was fluorinated by potassium fluoride and esterified by methanol to synthesize dimethyl tetrafluoroterephthalate. The ester was reduced with potassium borohydride and lithium chloride to give tetrafluoroterephthalyl alcohol. The above product was bromated in the hydrobromic acid to obtain 4-bromomethyl-2,3,5,6-tetrafluoro-benzene methanol. 4-Methyl-2,3,5,-6-tetrafluorobenzene ethanol was obtained by reducing the bromide with magnesium. In the exist of DCC and DMAP, tefluthrin was got by the condensation reaction between 4-methyl-2,3,5,6-tetrafluoro-benzene methanol and-(1RS,3RS)- 3-(2- chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cycolpropanecar-boxylate acid.

对苯二甲酸与氯气在碘存在下以发烟硫酸为溶剂进行氯化制备四氯对苯二甲酸;再以DMF为催化剂与二氯亚砜反应生成四氯对苯二甲酰氯;以氟化钾为氟化剂,环丁砜为溶剂置换氟化,再与甲醇酯化得到四氟对苯二甲酸甲酯;以KBH4-LiCl为还原剂二甲醚为溶剂反应制得四氟对苯二甲基苄醇;以氯苯为溶剂在溴化氢溶液中溴化得到溴化产物;在乙醇溶液中经镁粉还原得到4-甲基-2,3,5,6-四氟苄醇;甲基苄醇与功夫酸在催化剂二环己基碳二亚胺和4-二甲氨基吡啶作用下缩合得到七氟菊酯,总收率达43.6%。

The novel synthesis of the 2-hydroxyl α-arylglycines was realized through the Lewis acids promoted Friedel-Crafts reaction of phenols and N-tosyl imino ester in mild reaction conditions.

其中在路易酸TiCl〓促进下,酚类化合物和亚胺酯发生的傅克反应,可较高产率、较高区域选择性的得到2-羟基α-芳香甘氨酸衍生物。

In most cases, the medical profession do not advocate drug use of tea, in particular, ferrous sulfate, ferrous carbonate, iron citrate iron drink containing amine such as aluminum hydroxide of aluminum-containing agents, such as the western face of tea tea and more phenolic material and metal ion binding and precipitation, will be reduced or loss of efficacy.

在多数情况下,医学界不主张用茶水服药,尤其是硫酸亚铁、碳酸亚铁、枸橼酸铁胺等含铁剂喝氢氧化铝等含铝剂的西药,遇到茶汤中的茶多酚类物质与金属离子结合而沉淀,会降低或失去药效。

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