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乙酰

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Two ferrocenyl and trimethylsilyl substituted cyanohydrin ethers have been prepared by the addition of trimethysilyl cyanide to two acetyl-substituted ferrocenes: 1-(1-cyano-1-trimethylsilyloxyethyl)-ferrocene (1) and 1, 1'-bis(l-cyano-1-trimethylsilyloxyethyl)ferrocene (2). The structures of these two compounds were characterized by elemental analysis, IR, 1H NMR and X-ray crystallography.

通过两种取代的乙酰基二茂铁与三甲基氰硅烷的加成反应,得到两种取代二茂铁基三甲基硅烷基氰醇醚的晶体:1-(1-氰基-1-三甲基硅烷氧基乙烷基)二茂铁(1),1,1-二(1-氰基-1-三甲基硅烷氧基乙烷基)二茂铁(2),用X射线单晶衍射、元素分析、红外光谱和核磁共振氢谱对分子结构进行了表征。

Project Background and Conditions: The company started research new chemical products in 1998. After two years of efforts, a series of pharmaceutical intermediate sulfathiazole leave instructions, including : 3- methyl sulfathiazole leave instructions, 2- sulfathiazole leave instructions ethanoic acid, 2- acetyl sulfathiazole leave instructions, 2-thiofuran amino ethane ,2-thiofuran acetic, 3,4,5- tighter nitrobenzene have been successfully developed. 2-thiofuran amino ethane are the precursors raw materials of series antibiotic analgesic.

二、项目建设背景及条件:1998年公司开始研究开发高新精细化工产品,经过两年的努力,已成功研制出噻吩系列医药中间体,包括:3-甲基噻吩、2-噻吩乙酸、2-乙酰噻吩、2-噻吩乙胺、2-噻吩乙醇、3,4,5-三氯硝基苯等。2-噻吩乙胺系列噻吩产品使用于血小板及血栓有关的心脏血管病及消炎镇痛等如氯吡格雷、兴孢噻吩钠、兴孢西丁、噻吩洛酸等十几种新药的前体原料,是国家政策鼓励发展和有自主知识产权的项目。

Their specific surface area and acid strength were measured, and their catalyt and SBA-15 were ic performance was evaluated in the synthesis of fructone by acetalization of ethyl acetoacetate with ethylene glycol.

用浸渍法制备了一系列负载型磷钨酸及其铯盐催化剂,载体包括超稳Y沸石、脱铝超稳Y沸石、SiO2和SBA-15,测定了催化剂的比表面积和酸强度,并在乙酰乙酸乙酯与乙二醇液相缩合制取苹果酯反应中考察了催化剂的性能。

The synthesis of fructone from ethyl acetoacetate and ethylene glycol using sulfonated activated carbon as solid acid catalyst was investigated.

以活性炭磺化制得新型固体磺酸磺化炭为催化剂,对乙酰乙酸乙酯和乙二醇合成苹果酯的催化工艺进行了系统研究。

The strongly acidic cation exchange resin catalyzed synthesis of fructone-B by the reaction of ethyl acetoacetate and 1,2-propanediol was studied.

以硫酸高铈铵为催化剂,通过乙酰乙酸乙酯分别与乙二醇和1,2-丙二醇反应合成了苹果酯-A和苹果酯-B,研究了催化剂等有关因素对产品收率的影响。

The acyl derivatives all exhibited higher inhibitory effect than prinsepiol, among which isobutyryl and diacetate derivatives exhibited highest activity with EC50 of 3.85 mg/L and 5.60 mg/L respectively.

在Prinsepiol 4,4'位引入不同酰基后化合物的抑菌活性均有不同程度提高,其中4,4'-二异丁酰基衍生物和4,4'-二乙酰基衍生物的抑菌活性均较好,有效中浓度(EC50)分别为3.85和5.60 mg/L,是Prinsepiol的6~8倍。

This thesis consists of four chapters:Chapter 1: Michael addition of chalcones with active methylene compounds such as diethyl malonate, ethyl acetoacetate and nitromethane catalyzed by potassium hydroxide in anhydrous ethanol results Michael adducts in 72-98% yield under ultrasound irradiation in 25-150min.

第一章:研究了超声辐射下,氢氧化钾催化的查耳酮与活泼亚甲基化合物如丙二酸二乙酯、乙酰乙酸乙酯和硝基甲烷的迈克尔反应。

A series of polys based on pyromellitic dianhydride, biphenylyl tetracarboxylic dianhydride, thiodiphthalic dianhydride bis benzene dianhydride and oxydiphthalic dianhydride were prepared in different solvents.

以所合成的AB_2单体为原料,合成了一系粘度较低、溶解性良好,带端酚羟基、苯甲酰基、乙酰基、氰代苯基和苯酰苯亚胺基的芳香族超支化聚酰亚胺,通过核磁波谱、红外光谱分析和元素分析对其结构进行确证。

A series of lanthanide complexes (Ln = Er, Nd, Yb) with infrared emission properties were designed and synthesized by using different anionic ligands [1 -phenyl-3-methyl-4-(4-tertbutylbenzoyl)-5-pyrazolone and l-phenyl-3-methyl-4--5-pyrazolone and 2-naphtoyl trifluoroacetone] and netural ligands (2,2-dipyridine, phenanthroline, triphenylphosphine oxide and water). Three crystal structures of these complexes were obtained and structure studied, and the properties of photoluminescence and fluorescent lifetime were studied in detail.

我们通过选用不同的第一配体[1-苯基-3-甲基-4-(4-异丁酰基)-5-吡唑酮,1-苯基-3-甲基-4-(4-叔丁基苯甲酰基)-5-吡唑酮和2-萘基三氟乙酰丙酮]和第二配体(2,2-联吡啶,邻菲啰啉,三苯基氧膦)合成了16个稀土红外配合物(Ln=Er,Nd,Yb),获得了其中三个配合物的单晶结构,研究了这些稀土红外配合物的光致发光和荧光寿命等性质。

On the basis of the complex structures of AHAS and sulfonylureas inhibitors, systematic molecule docking study of five sulfonylureas inhibitors to AHAS were performed with autodock 3.0 package.

基于酵母乙酰羟酸合成酶与磺酰脲类抑制剂复合物的晶体结构,用分子对接方法对AHAS与5个磺酰脲类抑制剂相互作用的方式进行了系统的分子对接研究。

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