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chloro-acetophenone相关的网络例句

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Afterwards, N-(6-chloro-3-pyridinemethyl) phthalimide is prepared by using potassium phthalimide, as nucleophilic reagent, condensation reacting with 2-chloro-5-methylpyridine at a temperature of 70℃.

然后在70℃条件下,以邻苯二甲酸亚胺钾作为亲核试剂,与2-氯-5-氯甲基吡啶发生缩合反应,制备了N-(6-氯-3-吡啶甲基)邻苯二甲酰亚胺。

Then, N-(5-nitro-6-chloro-3-pyridinemethyl) phthalimide is obtained after the nitrating reaction of N-(6-chloro-3-pyridine methyl) phthalimide. The yield of the obtained product is 90.5%, and its melting point is 143.1~143.8℃.

缩合产物再经过硝化,合成N-(5-硝基-6-氯-3-吡啶甲基)邻苯二甲酰亚胺,其熔点为143.1~143.8℃,收率为90.5%。

Their structures were characterized by IR, 1H NMR, of which 4-chloro- 2-methyl-7-(2-bromoethoxy) isoflavone, 2, 4\'-dimethyl-7-(2-bromo-ethoxy)isoflavone and 2-methyl-7-(2-bromoethoxy) isoflavone are rarely reported so far.4\'-chloro-2-methyl-7-(3-bromopropoxy)isoflavone, 2, 4\'-dimethyl-7-(3-bromo- propoxy) isoflavone, 2-methyl-7-(3-bromopropoxy) isoflavone, 4\'-methoxy-2-methyl-7-(3-bromopropoxy) isoflavone and 4\'-hydroxy-2-methyl-7-(3-bromopropoxy) isoflavone were gained by reacting 7-hydroxy-2-methyl isoflavone derivatives with 1, 3-dibromo- propane, respectively.

第三章(来源:73ABC论文网www.abclunwen.com)在丙酮溶液中以K_2CO_3为碱,使溴乙氧基异黄酮和溴丙氧基异黄酮与咪唑偶合,以较高的产率合成出10种目标化合物:2-甲基-4′-氯-7-2-(1-咪唑基乙氧基异黄酮、2,4′-二甲基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-4′-甲氧基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-4′-羟基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-4′-氯-7-3-(1-咪唑基丙氧基异黄酮、2,4′-二甲基-7-3-(1-咪唑基丙氧基异黄酮、2-甲基-7-3-(1-咪唑基丙氧基异黄酮、2-甲基-4′-甲氧基-7-3-(1-咪唑基丙氧基异黄酮、2-甲基-4′-羟基-7-3-(1-咪唑基丙氧基异黄酮,经IR、~1H NMR、~(13)C NMR、元素分析等对其结构进行了表征,10种目标产物均未见文(来源:ABC论文cccccc网www.abclunwen.com)献报道。

A series of pyridazino[3,2-c]1,2,4-triazoles were synthesized from hydrazides and 3-aryl-6- chloro pyridazine s (3a~3d), which were obtained from substituted benzene and succinic anhydride by Friedel-Crafts reaction, cyclization with hydrazine hydrate, dehydrogenation and chloro-substitution.

以取代苯和丁二酸酐为起始原料,经Friedel-Crafts反应,肼合环,Br2/HOAc氧化脱氢后得到一系列1,6-二氢-3-芳基-6-哒嗪酮(2a~2d)。然后将2a~2d与PCl5在POCl3中回流,得到相应的氯代产物3a~3d,将其与酰肼作用,合环后得到一系列未见报道的哒嗪并[3,2-c]1,2,4-三唑类化合物。所有化合物结构均经元素分析,IR,1HNMR和MS谱得以证实,并对其波谱性质进行了讨论

In shallow well water disinfections effective 4~5% chlorineout of mother liquor of chloro-trisodium phosphate is used,30 minutes later chlorine reach 0.6 to 0.8 mg per liter (0.6~0.8 ppm),this water reach the national sanitary standed of drinking water mother liquor of chloro-trisodium phosphate can be best described as nonpoisonous,no remainer,quick and kill bacterium with wide-range,no corrosion and fine stability,safe,reliable new bactericide.

在浅井水消毒中,用有效氯为4.0—5.0%的氯化磷酸三钠母液投放,有效氯达到0.6—0.8mg/升(0.6ppm—O.8ppm)作用30钟后,该水可完全达到国家饮用水卫生标准。氯化磷酸三钠母液是一种无毒、无残留、速效广谱杀菌,无腐蚀性、稳定性好、安全可靠的新型杀菌剂。

A small cell-permeable compound, BH3I-2 3-iodo-5-chloro-N-[2-chloro-5-((4-chlorophenyl)sulphonyl phenyl]-2-hydroxybenzamide, has been recently reported to have a function similar to Bak BH3 peptide.

最近报道,可通透细胞的小分子化合物,BH3I-2':3-碘-5-氯-N-{2-氯-5-[(4-氯苯基)磺酰]苯基}-2-水杨酰胺具有与Bak BH3肽相似的作用。

A high performance liquid chromatographic method was studied for the simultaneous determination of pesticide imidacloprid and its two intermediates (2-chloro-5-methyl pyridine and 2-chloro-5-chloromethyl pyridin).

研究了用高效液相色谱法同时分离测定农药吡虫啉原粉和中间体2-氯-5-甲基吡啶及2-氯-5-氯甲基吡啶含量的方法。

Bezaldehyde was used as protective agent in first method.S-Epichloeohydrin was aminated and acidulated to give(2S)-1-Amino-3-chloro-propanol Salts.The acetylation of (2S)-1-Amino-3-chloro-propanol by acetic anhydride produced the intermediate-N-[2--3-chloropropyl]acetamide.And then at 20℃,in the presence of lithium tert-butoxide,benzyl 3-fluoro-4-morpholinophenyl carbamate react with-N-[2--3-chloropropyl]acetamide to give linezolid in total yield of 43.6%.

路线一采用苯甲醛作保护剂,使S-环氧氯丙烷氨解、酸化生成S-1-氨基-3-氯-2-丙醇盐酸盐,然后经乙酰化反应后,生成中间体-N-[2-乙酰氧基-3-氯丙基]乙酰胺,再用N-(3-氟-4-吗啉苯基)氨基甲酸苄酯和中间体在催化剂叔丁醇锂存在下25℃反应生成利奈唑酮,总产率达到43.6%。

For the asymmetric reduction ofα-hydroxyacetophenone and ethyl 4-chloro acetoacetate,-1-phenyl-1,2-ethanediol and-ethyl 4-chloro-3-hydroxybutanoate were produced by the purified enzyme, with the 99% and 94.3% e.e. value respectively.

在纯酶水平验证了近平滑假丝酵母(Candida parapsilosis CCTCCM203011)对外消旋苯基乙二醇的拆分机理,整个去消旋过程是由-苯基乙二醇次级醇脱氢酶和羰基还原酶共同催化完成的。

Using PbO2/Ti as anode,pure lead as cathode,H2SO4 as medium,MnSO4 was electrolyzed into Mnin a undivided cell,then,using Mnas oxidant, p-chloro-toluene was oxidized into p-chloro-phenylaldehyde.

采用无隔膜电解槽,以PbO2/Ti为阳极,纯Pb为阴极,MnSO4在H2SO4介质中电解为Mn,于电解槽外氧化对氯甲苯生成对氯苯甲醛。

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