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氯甲烷

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The structures were identified by IR, UV,〓 NMR and element analyses. 2. Free radical 4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxyl as catalyst, the phase transfer catalyzed method of oxidation eighteen semicarbazides to N-Aryl-2-Phenyl diazenecarboxamide with a solution of potassium ferricyanide in 2N aqueous sodium hydroxide and dichloromethane is described for the first time.

利用2,2,6,6-四甲基-4-羟基-1-哌啶氮氧自由基为相转移催化剂,在饱和铁氰化钾的2N氢氧化钠溶液与二氯甲烷的两相反应液中,催化氧化十八个取代氨基脲得到十八个相应的新型偶氮化合物N,2-二芳基二氮亚烯甲酰胺,均获得了较高的产率。

Results The tail formation rate of model group was significantly higher than the rate of control group (P<0.05) with a large number of Ⅲ and Ⅳ DNA damage cells. The tail formation rate of dichloromethane extraction groups were both significantly lower than the rate of model group (P<0.05). p53 mRNA expression of model group was higher than the rest except the crude Cornus Officinalis group.

结果 D-半乳糖致衰模型组小鼠骨髓细胞DNA拖尾率高于正常对照组(P<0.05),且Ⅲ、Ⅳ级损伤细胞数较多;山茱萸生品及制品二氯甲烷萃取部位组小鼠骨髓细胞DNA的拖尾率均低于D-半乳糖致衰模型组(P<0.05)。D-半乳糖致衰模型组小鼠骨髓细胞p53基因的表达高于正常对照组、阳性药组及制品组。

Optimization technology was acetidin: N-hexane (3:7) as low-pole solvent system, methanol: dichloromethane (1:9) as polar solvent system, 20% glycerol filter paper as moisturizer, 14 h age Bacillus subtilis as indicating strain seed on thin layer plate cultivated for 14~18 h, 1% TTC staining time 1~2 h, bacterial mix method suitable to 0.2%~0.6% agar semisolid bouillon culture-medium, bacterial spread method suitable to 1% agar semisolid bouillon culture-medium.

结果:该方法展开系统筛选简单,抑菌斑位置准确、斑点清晰,其优化条件为:以乙酸乙酯:正己烷(3:7)为弱极性展开系统,甲醇:二氯甲烷(1:9)为强极性展开系统,用20%甘油滤纸对湿室保湿,以14h菌龄的枯草芽孢杆菌为指示菌种子液,自显影薄层板36℃培养14~18h,1%TTC显色时间为1~2h,含0.2%~0.6%琼脂的半固体肉汤培养基应使用混菌法生物自显影,含1%琼脂半固体肉汤培养基应使用涂布法生物自显影。

My company's main products are R11, R12, R13, R22, R227, R502, R141b, R142b, R152a, R113, R134a, R402A (HP80), R402B (HP81), R404A (HP62), R123, R407C, R410A, R507 , Tsinghua series refrigerants, as well as some related products such as dichloromethane, chloroform, halons, refrigeration oil and blowing agent (R11, R245) and so on.

我公司的主要产品有 R11 、 R12 、 R13 、 R22 、 R227 、 R502 、 R141b 、 R142b 、 R152a 、 R113 、 R134a 、 R402A ( HP80 )、 R402B ( HP81 )、 R404A ( HP62 )、 R123 、 R407C 、 R410A 、 R507 、清华系列制冷剂,以及一些相关产品如二氯甲烷、三氯甲烷、聚四氟乙烯、冷冻油及发泡剂( R11 、 R245 )等。

The structure of the target compound was confirmed by elementary analysis and nuclear magnetic resonance spectroscopy .

通过元素分析、核磁共振氢谱对其结构进行了确认,并测得其在二氯甲烷溶液中的紫外吸收光谱和荧光光谱。

The results indicated that the highest yield of BOC-indigo was 97% in CH2Cl2, and the lowest one was in PGMEA. It showed that the yield of BOC-indigo increased with high polarity and low molecular volume of solvent.

从实验结果得知,以极性较强且分子体积较小的二氯甲烷作为反应溶剂,其合成隐性颜料产率可达到97.2%,较四氢呋喃产率多4.4%,且较丙二醇甲醚乙酸酯产率多7.4%。

With TEMPO(5 mol%) as the catalyst,N-methyl-N-phenyl-hydrazine(1.2 equiv.) as the amine source,the direct ortho-amination of 2-naphthols could be easily achieved.The reaction was carried out at room temperature under air atmosphere.

以5 mol%TEMPO为催化剂,1.2当量N-甲基-N-苯基肼作氨源,二氯甲烷为溶剂,空气中,室温下,实现了对2-萘酚邻位氨基化,可以高效的合成1-氨基-2-萘酚类化合物。

With TEMPO(5 mol%) as the catalyst,N-methyl-N-phenyl-hydrazine(1.2 equiv.) as the amine source,the direct ortho-amination of 2-naphthols could be easily achieved.

以5 mol%TEMPO为催化剂,1.2当量N-甲基-N-苯基肼作氨源,二氯甲烷为溶剂,空气中,室温下,实现了对2-萘酚邻位氨基化,可以高效的合成1-氨基-2-萘酚类化合物。

This article describes the low pressure fluorination process for production of dichlorodifluoromethane , discusses the problems of prevailing in the process and proposes an improved process-high pressure fluorination reactor with external circulation.

介绍了二氟二氯甲烷低压氟化反应的生产过程,指出和剖析了生产技术中存在的问题,提出了采用外循环加压氟化反应器的改进措施。改进后的反应器具有生产能力大,反应气质量好,催化剂损耗低等特

Dissolve the entire dry acetylation product in a minimum of methylene chloride in an Erlenmeyer flask.

用少量的二氯甲烷,把全部干的乙醯化产物溶解在锥形瓶中。

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这一模式非常关注商人的网络信用基础。

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