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The optimum synthetic conditions of ethyl chloroacetate are: molar ratio of chloroacetic acid to ethanol is 1:8, the quantity of catalyst[Fe2(SO4)3 xH2O] is 10% of the mass of chloroacetic acid, reaction time is 1 hour, 5A zeolite was used as dehydrating agent. In these conditions, the yield of ethyl chloroacetate was up to 73%.

用Fe_2(SO_4)_3·xH_2O作为催化剂合成氯乙酸乙酯的较佳反应条件是:酸醇物质的量之比为1:8,催化剂用量为氯乙酸质量的10%,以5A分子筛作为脱水剂,回流时间1h,收率达73%以上。

Trans-3-phenylglycidate ethyl ester was prepared from benzaldehyde and ethyl chloroacetate through Darzens condensation reaction.

以苯甲醛和氯乙酸乙酯为原料,经Darzens 缩合反应合成了反式-3-苯基缩水甘油酸乙酯,然后在25℃以氨水开环得赤型-3-苯基异丝氨酰胺。

In this paper, the applications of the environmental friendly solid acid catalysts for esterification were studied and the activities of these catalysts were discussed, by which the solid acid ferric sulfate x-hydrate was used first as catalyst in the synthesis of dimethyl fumarate and ethyl chloroacetate and solid super acid SO42-/Fe2O3 was used first as catalyst in the synthesis of ethyl p-nitrobenzoate.

本文研究了对环境友好的固体酸催化剂在酯化反应中的应用,首次以固体酸Fe_2(SO_4)_3·xH_2O为催化剂合成了新型防霉剂富马酸二甲酯和化工原料氯乙酸乙酯,以固体超强酸5O_4~(2-)/Fe_2O_3为催化剂合成了医药中间体对硝基苯甲酸乙酯,并探讨了这些催化剂的催化活性。

Chondrus ocellatus was extracted by methanol, ethanol, ethyl ether, ethyl acetate, petroleum ether and acetone, respectively.

采用甲醇、乙醇、乙醚、乙酸乙酯、石油醚、丙酮6种溶剂分别对角叉菜进行冷浸提取。

In order to isolate the active compounds in ethyl acetate fraction of Psoralea corylifolia L., activity-guided isolation was performed along with chromatographic techniques. Four active compounds were isolated from ethyl acetate fraction and identified by their NMR spectral data and physical-chemical properties. They are corylin and bavachin, which showed stimulating effect on osteoblastic proliferation and differentiation, isopsoralen and psoralen exhibited activity of promoting cell differentiation in some degree.

为了追踪分离补骨脂乙酸乙酯萃取物中的活性成分,本实验采用多种色谱分离技术,以活性测试为导向,结合波谱技术及理化数据,从补骨脂乙酸乙酯萃取物中分离并鉴定了4个活性化合物的化学结构,它们是具有促进细胞增殖和分化作用的补骨脂异黄酮和补骨脂二氢黄酮,对细胞分化有一定促进作用的异补骨脂素和补骨脂素。

In this catalyst system, the Knoevenagel condensations of a series of aromatic aldehydes with malononitrile or ethyl cyanoacetate were programmed and a mechanism was postulated as well. When aromatic aldehydes reacted with ethyl cyanoacetate, the corresponding alkenes proved to be E-isomers by 1H NMR.

在该反应体系中考察了一系列芳香醛和丙二氰、氰基乙酸乙酯的缩合反应,并推测了Knoevenagel缩合反应的机理,芳香醛与氰基乙酸乙酯缩合产物经1H NMR检测为E式烯烃。

The main compositions of LP are shorter chain carboxylic acid and their ethyl esters, furan derivatives, cyclopentanone, phenol derivatives, benzene derivatives, aromatic ketone, aromatic acid derivatives, longer chain carboxylic ethyl esters and sterides. After upgrading, the main indexes reach the standard of fuel oil.

结果表明,LP的主要成分包括短链或环状脂肪酸及其酯、呋喃衍生物、环戊烯衍生物、苯酚衍生物、苯衍生物、芳酮、芳酸及其乙酯、长链脂肪酸乙酯和甾族化合物,经提质其主要指标达到了燃料油的标准。

A novel type of amphiphilic tri-block copolymers with both pH and temperature sensitiveness: poly-poly (dimethylamino ethyl methacrylate)-poly (ε-caprolactone)(PEG-PDMAEMA-PCL) was synthesized via sequential oxyanionic polymerization of macro-molecular: PEG, with a hydroxyl at one end, and dimethylamino ethyl methacrylate andε-caprolactone, with the potassium naphthalene as the initiator.

在本文中,报道了一类新型的兼具pH和温度敏感的双亲性嵌段共聚物:聚乙二醇-聚甲基丙烯酸N,N-二甲氨基乙酯-聚己内酯(PEG-PDMAEMA-PCL)及聚甲基丙烯酸N,N-二甲氨基乙酯-聚己内酯(PDMAEMA-PCL)的制备;并利用动态光散射和氢核磁共振光谱(~1H NMR)对该嵌段共聚物的水溶液性质进行研究;在此研究结果的基础上,初步探讨了其在仿生物矿化中的应用。

In order to investigate the mechanism for this reac-tion, methyl α-bromoacetate or ethyl α-bromoacetate as starting material was added to the solution of phenyl selenoamide in ethanol in 1∶1 or 2∶1 molar ratio under the neutral condition at room temperature. The results indicated that the same product bis or bis diselenide was formed. Byproduct ethyl benzoate was also separated.

为了研究该反应机理,选择α-溴代乙酸甲酯或α-溴代乙酸乙酯在无催化剂、中性条件下,乙醇溶液中与苯基硒代酰胺室温下反应,投料比为1∶1和2∶1,结果也都生成了同一类产物二甲氧羰基甲基二硒醚或二乙氧羰基甲基二硒醚,同时还分离得到了相应的副产物苯甲酸乙酯。

In order to investigate the mechanism for this reaction, methyl α-bromoacetate or ethyl α-bromoacetate as starting material was added to the solution of phenyl selenoamide in ethanol in 1:1 or 2:1 molar ratio under the neutral condition at room temperature. The results indicated that the same product bis or bis diselenide was formed. Byproduct ethyl benzoate was also separated.

为了研究该反应机理,选择α-溴代乙酸甲酯或α-溴代乙酸乙酯在无催化剂、中性条件下,乙醇溶液中与苯基硒代酰胺室温下反应,投料比为1:1和2:1,结果也都生成了同一类产物二甲氧羰基甲基二硒醚或二乙氧羰基甲基二硒醚,同时还分离得到了相应的副产物苯甲酸乙酯。

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