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To be different from the already chloromethylation catalyst, it has a certain amount of moisture wet, which will not produce huge amounts of doughtic cancerogenic chloromethyl methyl ether during and after the reaction.4,4\'-bisbiphenyl, 1,4-bisbenzene, 1,4-bis(chloro- methyl)-2,5-dimethylbenzene, 1,5-bis-2,4-dimethylbenzene, 4-(chlor- omethyl)-1,2-dimethylbenzene, 1,2-bis-4,5-dimethylbenzene, 5,8-bis-1,2,3,4-tetrahydronaphthalene, 3,3\',5-tris-4,4\'-bisbiphenyl and 3,3\', 5,5\'-tetrakis-4,4\'-bisbiphenyl were synth- esized by using this new catalyst. Results indicated that when the reaction temperature was 55~60℃, the reaction time was 12h, the catalyst which consists of the concentration of 80%H_2SO_4, HAc and Lewis acid, the amount of Lewis acid 0.15 mol(nLewis:nbiphenyl=1.5:1), yield of biphenyl chloromethylation product 4,4\'-bis(chrolomethylbiphenyl can reach a maximum 85%.

采用这种催化体系完成了4,4′-二氯甲基联苯、对二氯甲基苯、1,4-二氯甲基-2,5-二甲基苯、1,5-二氯甲基-2,4-二甲基苯、4-氯甲基-1,2-二甲基苯、1,2-二氯甲基-4,5-二甲基苯、5,8-二氯甲基-四氢萘、3,3',5-三氯甲基-4,4'-二甲基苯和3,3',5,5'-四氯甲基-4,4'-二甲基苯的合成,结果表明:在反应条件为:反应温度55~60℃,反应时间12h,选择80%H_2SO_4、冰醋酸和Lewis酸为催化剂,反应最佳反应Lewis酸用量是0.15mol(和原料比为1.5:1),反应效果最好,联苯氯甲基化产物(4,4′-二氯甲基联苯)收率为85%;在反应条件为:反应温度70℃,反应时间8h,80%H_2SO_4、冰醋酸和Lewis酸为催化剂,反应最佳反应Lewis酸用量是0.1mol(和原料比为1:1)时,反应效果最好,苯的氯甲基化产物收(来源:ABd0C论文eded网www.abclunwen.com)率为75%;在反应条件为:在反应条件为:反应温度40℃,反应时间10h,60%H_2SO_4和Lewis酸为催化剂,反应最佳反应Lewis酸用量是0.1mol(和原料比为1:1)时,反应效果最好,对二甲苯氯甲基化产物(1,4-二氯甲基-2,5-二甲基苯)收率为78.5%;在反应条件为:反应温度35℃,反应时间10h,60%H_2SO_4、冰醋酸和Lewis酸为催化剂,反应最佳反应Lewis酸用量是0.1mol(和原料比为1:1)时,反应效果最好,间二甲苯氯甲基化产物(1,5-二氯甲基-2,4-二甲基苯)收率为81.5%。

This dissertation is mainly focused on the reactivity of methylenecyclopropanes and comprises six parts. 1 The reactions of methylenecyclopropanes with phenylsulfenyl chloride, phenylselenyl chloride and diphenyl diselenide; 2 The coupling reactions of the ring-opening products derivated from methylenecyclopropanes; 3 The palladium-catalyzed ring-enlargement of mono-aryl group substituted methylenecyclopropanes to cyclobutenes. 4 The gold-catalyzed domino ring-opening and ring-closing hydroamination of methylenecyclopropanes with sulfonamides; 5 The Lewis acid-catalyzed reactions of mono-aryl group substituted methylenecyclopropanes with diethyl ketomalonate in the presence of water; 6 The iodobenzene diacetate mediated novel 1,3-dipolar cycloaddition of methylenecyclopropanes, vinylidenecyclopropanes, and methylenecyclobutane with phthalhydrazine.

本论文主要研究了亚甲基环丙烷类化合物的一些化学反应性能,共由以下六部分组成:1、亚甲基环丙烷类化合物与苯硫氯、苯硒氯及二苯基二硒的反应;2、亚甲基环丙烷类化合物开环产物的偶联反应;3、单芳基取代的亚甲基环丙烷类化合物在钯催化剂作用下的扩环反应;4、金化合物催化磺酰胺对亚甲基环丙烷类化合物的串联开环关环氨氢化反应;5、路易斯酸催化亚甲基环丙烷类化合物与丙酮二羧酸二乙酯在有水存在下的反应;6、醋酸碘苯促进的亚甲基环丙烷类化合物、亚乙烯基环丙烷类化合物及亚甲基环丁烷类化合物与邻苯二甲酰肼的新型1,3-偶极环加成反应。

Professional sales companies operating bromide products: sodium bromide, sodium bromide, potassium bromide, potassium bromate, Tetrabromobisphenol A, Deca-BDE, ten PBDEs, DBDPE, hexabromodiphenyl Central dodecane, dibromo neopentyl glycol, neopentyl bromide three alcohols, three bromine phenol, octabromodiphenyl ether, brominated polystyrene, bromide, calcium bromide, dibromo succinic acid, dibromo-D ene glycol, bromide surfactants series: Dodecyl trimethyl ammonium bromide, tetradecyl trimethyl ammonium bromide, cetyltrimethyl ammonium bromide, octadecyl trimethyl ammonium bromide dodecyl trimethyl ammonium chloride, tetradecyl trimethyl ammonium chloride, cetyl trimethyl ammonium chloride, octadecyl trimethyl ammonium chloride, tetrabutyl ammonium bromide wholesale sales: dimethylolpropionic acid, DL-malic acid, isophthalic acid PIA, glycolic acid, adipic acid.

公司专业经营销售溴化物系列产品:溴化钠、溴酸钠、溴化钾、溴酸钾、四溴双酚A、十溴二苯醚、十溴联苯醚、十溴二苯乙烷、六溴环十二烷、二溴新戊二醇、三溴新戊醇、三溴苯酚、八溴醚、溴化聚苯乙烯、溴化铵、溴化钙、二溴丁二酸、二溴丁烯二醇、溴化表面活性剂系列:十二烷基三甲基溴化铵、十四烷基三甲基溴化铵、十六烷基三甲基溴化铵、十八烷基三甲基溴化铵、十二烷基三甲基氯化铵、十四烷基三甲基氯化铵、十六烷基三甲基氯化铵、十八烷基三甲基氯化铵、四丁基溴化铵批发销售:二羟甲基丙酸、DL-苹果酸、间苯二甲酸 PIA、羟基乙酸、己二酸。

Studies on Synthesis and Crystal Structure of N, N'-Bis(4-Hydroxy-3-Methoxybenzyl) Oxalamide

篇名 N,N'-双(4-羟基-3-甲氧基苯甲基)草酰胺的合成及晶体结构研究

The new oxalamide bridging ligands N, N'-bis (4-hydroxy-3-methoxy-benzyl) oxalamide (H4LB) was designed and synthesized.

设计合成一种新型对称的草酰胺桥联配体:N,N'-二(4-羟基-3-甲氧基苯甲基)草酰胺配体(H4LB)。

In the first part, five new 4-acyl pyrazolone 4-ethyl-thiosemicarbazones compounds: 1-Phenyl-3-methyl-4-(4-bromo)benzal-pyrazol-5-one N(4)-ethyl-thiosemicarbazone (PM4Br BP-ETSC), 1-Phenyl-3-methyl-4-(4-methyl)benzal-pyrazol-5-one N(4)-ethyl-thiosemicarbaz -one (PM4MBP-ETSC), 1-Phenyl-3-methyl-4-benzal-pyrazol-5-one N(4)-ethyl-thiosemicarba -zone, 1,3-diphenyl-4-benzal-pyrazol-5-one N(4)-ethyl-thiosemicarbazone and 1-Phenyl-3-methyl-4-phenylacetyl-pyrazol-5-one N(4)-ethyl-thiosemi -carbazone have been synthesized and characterized by elemental analyses, IR, 1H NMR spectra and single-crystal XRD.

第一部分合成了五个4-酰基吡唑啉酮缩4-乙基-氨基硫脲化合物:1-苯基-3-甲基-4-(4-溴)苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲(PM4BrBP-ETSC),1-苯基-3-甲基-4-(4-甲基)苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲(PM4MBP-ETSC),1-苯基-3-甲基-4-苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲,1,3-二苯基-4-苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲和1-苯基-3-甲基-4-苯乙酰基-5-吡唑啉酮缩4-乙基-氨基硫脲,其中前四个具有光致变色性质。

Not long ago , it was found that levocetirizine displayed a better pharmacological profile than the racemic mixture .

但其它的二苯甲基类哌嗪化合物情况如何并不知道。

A biradical TN3 was synthesized, which is composed of a fully substituted triphenylmethyl radical and a nitroxide.

新开发的双自由基(TN3)由全取代三苯甲基自由基和氮氧自由基两部分组成。

Effects of reaction temperature, reaction time, the amount of alkali, benzyl chloride and quaternary ammonium on grating rate of benzylated natural bamboo fiber have been discussed.

以接枝率为考察目标用正交试验探索了反应温度,碱用量,反应时间,氯化苄及助剂季铵盐的用量5个因素对天然竹纤维苯甲基化改性的影响,确定了最佳反应条件。

Meldrum is a carboxyl-phthalocyanine weak resistance agent, with the activity of this enzyme metal ion (Mg2 + Mg2 +) formed fairly stable chelate, and its derivatives benzene methyl malonic acid is a strong resistance agent.

丙二酸是一个羧基酞酶的弱阻化剂,它与这种酶的活性金属离子(镁离子Mg2+)形成相当稳定的螯合物,而它的衍生物苯甲基丙二酸则是一个强阻化剂。

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Now, however, all children continue in "comprehensive" schools, and the eleven-plus determines which courses of study the child will follow.

然而现在,所有的孩子都要在综合学校继续学习,所以这次考试只是决定他们将要学习哪些课程。

Cultivatable land , and led to a general recognition that development must not be carried at the cost of agriculture .

城区的迅速扩大在很多情况下侵占了宝贵的可耕地,使人们普遍认识到发展不能以牺牲农业为代价。

Detailed Intrinsic Reaction Coordination calculations were carried out to guarantee the optimized transition-state structures being connected to the related tautomers.

同时,做了详尽的内禀反应坐标计算,以保证所得到的过渡态连接相应的始末异构体。