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Ethyl 4-[(1-hydroxy-1-methyl)ethyl]-2-propyl-1H-imidazole-5-carboxylate,the key intermediate of Olmesartan ,was synthesized from butanoic acid and o-phenylenediamine via condensation under microwave-irradiation,oxidation,esterification and the Gringard reaction.

用正丁酸与邻苯二胺为原料,在微波照射下缩合成2-丙基苯并咪唑,再氧化开环制得2-丙基咪唑二羧酸,再经酯化、Gringard反应制得抗高血压药物奥美沙坦的关键中间体2-丙基-4-[(1-羟基-1-甲基)乙基]-1H-咪唑-5-羧酸乙酯,总收率32.2%。

The results showed that hexadecanoic acid diethanolamide and Daqing crude oil has favorable compatibleness, the binary system containing hexadecanoic acid diethanolamide(with the mass concentration of 0.2%) and HPAM(with the concentration of 1000mg/L)can produce ultralow interficial tensions 8.94×10~(-3mN/m against Daqing crude oil; the three compound combination system containing hexadecanoic acid diethanolamide(with the mass concentration of 0.2%) and HPAM(with the concentration of 1000mg/L)and Na_2CO_3(0.1%)can produce ultralow interficial tensions 6.34×10~(-4mN/m against Daqing crude oil.

其中,十六酸二乙醇酰胺与大庆四厂原油具有良好的配伍性,十六酸二乙醇酰胺0.2%、HPAM1000mg/L组成的二元驱油体系与大庆四厂原油可形成超低界面张力,最低可达到8.94×10~(-3)mN/m;十六酸二乙醇酰胺0.2%、HPAM1000mg/L、Na_2CO_31%组成的三元驱油体系与大庆四厂原油间的界面张力最低可达6.34×10~(-4)mN/m。

Silicon phthalocyanine dihydroxide was prepared from silicon phthalocyanine dichloride through two methods. The first was alkali treating that meaned silicon phthalocyanine dihydroxide was treated in the ethanol solution containing sodium methylate .The second was acid treating meaned precipitating its solution in concentrated sulfuric acid into ice water. The product yield of the second method was 77.0%, which was higher than the method of alkali treating.

此外将合成的二氯酞菁硅采用两种方法转化为二羟基酞菁硅,第一种方法是碱处理法即将二氯酞菁硅在甲醇钠的乙醇溶液中回流得到,最高收率为53%第二种方法是酸处理法即采用二氯酞菁硅的硫酸溶液在冰水析出的方法转化为二羟基酞菁硅,其中酸溶析出法收率为77.0%。

The ammonia was evaporated under decreasing pressure, and the precipitate was filtered off and the liquid was poured into hot saturated picric acid solution to get picrate with a yield of 85.0%. The optimum process starting from imidazole-4,5-dicarboxylic acid was: imidazole-4,5-dicarboxylic acid in acetic anhydride was refluxed to get imidazole-4-carboxylic acid, and the product was esterification in ethanol with a catalyzer of concentrated sulfuric acid to get ethyl imidazole-4-carboxylate, at last the compound above was reduced by LiAlH4 in ether at room temperature to get the target compound, the total yield of this route was 49.6%.

以4,5-二羧酸咪唑为原料的较佳工艺:1 脱羧反应:4,5-二羧酸咪唑40g,醋酐1200ml,回流10h,过滤并将滤液浓缩至干,所得固体加至50%的乙醇溶液回流,过滤并将滤液自然冷却过夜,过滤得固体;2 酯化反应:4(5)-羧酸咪唑50g,乙醇1000ml和浓硫酸60ml,加热回流2h,5%浓度NaOH溶液调节至pH=8,减压浓缩至干,加入少量水回流,自然冷却过夜并过滤得固体;3 还原反应:LiAlH410g,乙醚300ml和4(5)-羧酸咪唑乙酯28g,常温反应1.5h,小心滴加25ml水后过滤,滤渣溶于300ml甲醇中并过滤,收集所得乙醚和甲醇滤液浓缩至干,将所得固体溶于300ml乙醇中加热回流,后将溶液浓缩至约30ml,冷却并过滤得固体,该路线总收率为49.6%。

We introduce two pyridinedicarboxylate (2,5-H2pdc and 2,6-H2pdc) ligands, under hydrothermal or solvothermal condition, to yield 7 complexes with InCl3. Complex 17 presents a rare example of chiral binodal (4,8)-connected lattice with self-interpenetration.

选择了两种吡啶二羧酸配体: 2,5-吡啶二羧酸(2,5-H2pdc); 2,6-吡啶二羧酸(2,6-H2pdc)和InCl3反应合成了七个配位化合物其中17表现了一例少有的手性的(4,8)连接的双节点自穿插拓扑结构。

These compounds were identified as follows:chrysophanol (FP-1),physcion(FP-2),eriosematin(FP-3),scoparone(FP-4),lupeol(FP-5),betulinic acid(FP-6),3\',4\'-Dihydroxy-trans-cinamic acid octacosyl ester(FP-7),β-sitosterol (FP-8),flemiphilippinone A(FP-9),monopalmitin(FP-10),emodin(FP-11),islandicin (FP-12),salicylic acid(FP-13),p-methoxyphenylpropionic acid(FP-14),trideca-1, 3-diene(FP-15),lupinifolin(FP-16),flemichin D(FP-17),flemiphilippinin A(FP-18), auriculasin(FP-19),erythrinin B(FP-20),6-C-prenylluteolin(FP-21), 8-(1,1-dimethylallyl) genistein(FP-22),flemiphilippinin E(FP-23),flemiphilippinin F (FP-24),5,7,3\',4\'-tetrahydroxy-6,8-diprenylisoflavone(FP-25),flemiphilippinin D (FP-26),dorsmaninsⅠ(FP-27),osajin(FP-28),6,8-diprenyleriodictyol(FP-29), lupinalbin A(FP-30),genistein(FP-31),3\'-O-methylorobol(FP-32),orobol(FP-33), 5,7,2\',3\',4\'-pentahrdroxyflavone(FP-34),the mixture of biochanin A and prunetin (FP-35 and 36),genistin(FP-37),sophororicoside(FP-38),3\'-O-methylorobol-7-glucoside(FP-39),the mixture of sissotrin and prunetin 4\'-O-β-D-glucoside(FP-40 and 41),adenosine(FP-42) and luteoloside(FP-43,mixture).

这些化合物分别为大黄酚(FP-1)、大黄素甲醚(FP-2)、eriosematin(FP-3)、滨蒿内酯(FP-4)、羽扇豆醇(FP-5)、白桦酸(FP-6)、咖啡酸二十八烷酯(FP-7)、β-谷甾醇(FP-8)、蔓性千斤拔酮A(FP-9)、单棕榈酸甘油酯(FP-10)、大黄素(FP-11)、islandicin(FP-12)、水杨酸(FP-13)、对甲氧基苯丙酸(FP-14)、十三烷-1,4-二烯烃(FP-15)、lupinifolin(FP-16)、千斤拔素D(FP-17)、蔓性千斤拔素A(FP-18)、auriculasin(FP-19)、erythrinin B(FP-20)、6-C-异戊烯基木犀草素(FP-21)、8-(1,1-二甲烯丙基)-染料木黄酮(FP-22)、蔓性千斤拔素E(FP-23)、蔓性千斤拔素F(FP-24)、5,7,3′,4′-四羟基-6,8-双异戊烯基异黄酮(FP-25)、蔓性千斤拔素D(FP-26)、dorsmaninsⅠ(FP-27)、osajin(FP-28)、6,8-双异戊烯基圣草素(FP-29)、lupinalbin A(FP-30)、染料木黄酮(FP-31)、3\'-O-甲基香豌豆苷元(FP-32)、奥洛醇(FP-33)、5,7,2′,3′,4′-五羟基黄酮(FP-34)、鹰嘴豆素甲和樱黄素的混合物(FP-35和FP-36)、染料木苷(FP-37)、槐属苷(FP-38)、7-葡萄糖基-3\'-O-甲基香豌豆苷(FP-39)、印度黄檀苷和樱黄素4′-O-β-D-葡萄糖苷的混合物(FP-40和FP-41)、腺嘌呤核苷(FP-42)和木犀草苷(FP-43,混合物)。

Raman spectrum of saturated aqueous solution of ammonium dimolybdate crystal was recorded, and compared with those of ammonium dimolybdate crystal , ammonium heptamolybdate crystal, saturated aqueous solution of ammonium heptamolybdate crystal and monomolybdate anion in aqueous solution respectively.

记录了常温下二钼酸铵晶体饱和水溶液的Raman光谱,并分别与二钼酸铵晶体、仲钼酸铵晶体、仲钼酸铵晶体饱和水溶液、水溶液状态下单钼酸根离子的Raman光谱进行了比较研究。

In earlier studies, major classes of triacylglycerols were separated on the basis of unsaturation (i, e., trisaturated, disaturated, diunsaturated, and triunsaturated ) via fractional crystallization and oxidation-isolation methods.

早期的研究,在研究不饱和现象的基础上,通过分级结晶和氧化-分离方法,将三酰基甘油分为几类(如三饱和酸、二饱和酸、二不饱和酸和三不饱和酸)。

The environmental black direct dyestuff without carcinogensis was prepared by 4,4'- diamino - dibenzidine - 2 - sulfonicacid, 1 - hydroxy - 7 - aminonaphthalene - 3,6 - dusuifonicacid, m - benzoic - diamine and aniline.

以4,4'-二氨基-二苯胺-2-磺酸代替苯胺,与1-羟基-7-氨基-3,6-二萘磺酸、间苯二胺、苯胺等合成无致癌作用的环保型黑色直接染料。

The invention relates to a preparation and separation method of docosapentaenoic acid methyl ester and docosahexaenoic acid methyl ester.

本发明涉及二十二碳五烯酸甲酯和二十二碳六烯酸甲酯的制备和分离方法。

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