The hexyl acetate was synthesized from n-hexanol and acetic acid by direct esterification.

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Six derivatives of 4-phenyl-3-phenoloxymethyl-5-mercapto-1,2,4-triazlyole were synthesized from phenoloxyacetyl hydrazide by two-steps reaction under microwave irradiation, then reacted with 2-chloroacetic acid to give six novel derivatives of 2-(3-phenoxymethyl-4-phenyl-[1,2,4]triazole-5-thio)-acetic acid.

在微波輻射條件下，芳氧乙酰肼經(jīng)兩步反應(yīng)制得4-苯基－3-芳氧甲基－1丰满熟妇精品乱又伦免费看，2，4-三唑－5-硫酮衍生物人人超碰喷潮人人，再與氯乙酸反應(yīng)得到6種尚未見文獻(xiàn)報(bào)道的2-（3-芳氧甲基－4-苯基－1国产自慰网站，2，4-三唑－5-硫基）乙酸衍生物免费欧美性交。

Hydroxy benzene acetic acid and acetic acid have biological activity, such as anti-bacterial and other aspects, a wide range of applications.

苯羥基乙酸和苯氧乙酸都具有生物活性天天碰人人摸人人操，在諸如抗菌等方面具有廣泛的應(yīng)用。

Whole cell currents evoked by NMDA, AMPA or kainite were slightly influenced by sparfloxacin, felbinac, or sparfloxacin plus felbinac.

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The conversion of acetic acid and the selectivity of propylene reached 85.43% and 98.52%, respectively.

本文還對(duì)乙酸與丙烯直接酯化合成乙酸異丙酯的動(dòng)力學(xué)進(jìn)行了研究久久天堂网av。

The results indicated that they all had certain effect, but potassium sorbate and sodium diacetate were better than others.

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Esterification of terpineol with oxalic acid, chloroacetic acid and trichloroacetic acid by solid superacid MoO3/TiO2 was studied.

研究了MoO3/TiO2固體超強(qiáng)酸催化劑催化松節(jié)油與草酸亚洲一级一片黄a久久，氯乙酸，三氯乙酸反應(yīng)的規(guī)律女人爽到呻吟的在线观看视频。

A series of p-toluene sulfonylamido acetacylhydrazone derivatives were synthesized from p-toluenesulfonyl chloride which reacted with glycine to get the intermediate p-toluene sulfonylamido glycine, then through the esterification, hydrazinolysis to afford another intermediate p-toluene sulfonylamido acethydrazide, which condensed with different aldehydes to obtain the target compounds that were characterized by IR, 1H NMR, 13C NMR spectra and elemental analysis.

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D., 5m. The mobile phase consisted of a ternary gradient: methanol, 0.8% acetic acid and 0.01mol/L ammonic acid.

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Replacement of one benzimidazole fragment with benzothiazole or benzoxazole and optimization of the structure to create the new frame of the compounds were also carried out with the exception to find more potent compounds. The purpose of design and synthesis of these compounds is to investigate the QSAR of this class of compounds with the inhibition of HCV NS3/NS4A protease and eventually to develop more potent inhibitors.

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