本论文合成了一系列苯氧基（苯胺基）多元羧酸化合物。
In this paper, we synthesized a series of phenoxy-(phenylamino) polycarboxylic compounds.
提供了用于递送活性剂的氰基苯氧基羧酸化合物及其组合物。
Cyanophenoxy carboxylic acid compounds and compositions for the delivery of active agents are provided.
易感期饮水投放羟氨苄青霉素或苯氧基甲基青霉素，连续4-5天。
Medicate the water amoxycillin or phenoxymethylpenicillin for 4 - 5 days over the period of risk.
间苯氧基苯乙酮可由酚钾与间溴苯乙酮在醋酸铜催化下以高产率合成。
Phenoxyacetophenone could be prepared from potassium phenolate and m bromoacetophenone via Ullmann reaction catalyzed by copper acetate in high yields.
研究了化妆品中的甲基异噻唑啉酮、免洗消毒剂以及苯氧基乙醇推进剂的抗菌活性。
What's more, it studied the antibacterial activity of methyl lisothiazolinone, rinse-free disinfectants and phenoxyethanol.
柔性覆铜板用1,4 -双(2,4 -二氨基苯氧基)苯型聚酰亚胺薄膜的制备方法。
Method for preparing 1, 4-di (2, 4-diamino phenoxy) benzenoid form polyimide film for flexible copper clad plate.
以苯酚、环氧氯丙烷为原料，KOH为催化剂，肼解后合成了1—氨基—3—苯氧基—2—丙醇。
The 1-amino-3-phenoxyl-2-propanol is prepared with phenol and epoxy chloropropane by means of KOH as catalyst and hydrazinolysis.
以二苯醚与苯甲酰氯为原料，合成了一种新型的激光光敏刺——4 -苯氧基二苯甲酮(PBZP)。
A new photoinitiator, 4-phenoxy benzophenone (PBZP), was synthesized and characterized using diphenyl ether and benzoyl chloride as raw material.
在选定的色谱操作条件下，2-（4-羟基苯氧基）丙酸与杂质对苯二酚等之间具有良好的分高效果。
Under the selected conditions of the chromatographic operation, there was the better separation efficiency between 2-(4- hydroxyphenoxy) propionic acid and impurities(such as hydroquinone, etc).
研究出用价廉、易得，能够方便自产的间—苯氧基苄基三乙基氯化铵作为相转移催化剂，获得了较好的结果。
Authors have obtained by using m-phenoxybenzyltriethylammonium chloride as the phase transfer catalyst which is cheap, available and self—productive. We hare achieved better results.
其中，化合物1是一个以线性四核铜配合物为基本单元的一维链聚合物，此时水杨醛缩苯氧基乙酰腙配体L1是五啮配体。
The adjacent complex molecules 1 are linked by N-N bridge of the pentadentate ligand L1, resulting in an one-dimensional polymer.
用苯酚和钠得到苯酚钠，苯酚钠和2-氯乙醇得到2-苯氧基乙醇，与氯化锌反应得2，3-二氢苯并呋喃，产率50%。
A mixture of phenol, sodium and 2-chloroethanol forms 2-phenoxyethanol, add zinc chloride, the product is 2,3-dihydrobenzofuran, yield 50%.
以邻甲氧基苯酚与对氯*为原料，经四步反应合成6-（2-甲氧苯氧基）-1，4-二氢-4-氧代-3-喹啉羧酸乙酯。经抗鸡球虫实验证明具有抗球虫效果。
The compound 6-(2-methoxy phenoxy)-1, 4-dihydrogen-4-oxo-3-ethyl quinoline carboxylate is prepared with o-methoxyphenol and p-chloronitrobenzene as materials and through four-step reaction.
通过4-甲氧基苯甲醛的羰基加成反应合成4-甲氧基-苯基羟基乙酸。
The 4-methoxy-phenylhydroxy-acetic acid was synthesized by the carbonyl addition reaction of 4-methoxybenzaldehyde.
在最佳条件下产品邻甲氧基二苯醚的收率可达到84.6%。
The yield of the product under optimum conditions was up to 84.6%.
结论3，5 二硝基苯甲酰氧基作为良好的糖端基离去基用于寡糖的合成，具有反应条件温和、收率较高、立体选择性好的特点。
Conclusion The 3, 5-dinitrobenzoyl group was found to be a good leaving group at the anomeric position and O-glucopyranosides and oligosaccharides were stereoselectively synthesized in good yield.
报道了用GC／MS方法及衍生化技术研究6甲氧基正丁苯酞（MBP）在大鼠肝微粒体中的代谢转化结果。
The in vitro biotransformation of 6 methoxy butyl phthalide (MBP) by phenobarbital induced rat liver microsomes was investigated by GC/MS and GC/MS with TMS derivatization.
研究结果表明化学结构适易的烷氧基苯甲醛氧化产率大于90 %。
The experimental results indi- cate that oxidation yields of some alkyloxybenzaldehydes are above 90 % .
以乙醇为溶剂，碘化钠为催化剂，由金属钠、对苯二酚和溴丁烷合成了1 ，4 -二丁氧基苯。
With ethyl alcohol as solvent and sodium iodide as catalyst, 1,4-dibutoxybenzene was synthesized from metal sodium, hydroquinone and n-butyl bromide.
目的研究微波合成苄氧基苯甲醛的最佳反应条件。
Objective To study Optimization of the react conditions of benzyloxy-benzaldehyde synthesized under microwave irradiation.
目的：探索4（2氯乙氧基）二苯酮的合成条件，包括原料配比、反应时间等。
Objective:In order to find the best condition for the synthesis of 4 (2 chloroethoxy)benzophenone, including the proportion of material, the time of reaction.
本课题以二茂铁为原料，与邻甲氧基苯甲酰氯反应生成邻甲氧基苯甲酰基二茂铁，再与一系列胺反应合成亚胺，最终还原为二茂铁氨基化合物。
The title compounds were obtained by the reduction of the corresponding ferrocenyl imines, which were prepared from ferrocene and o-anisic acid chloride, followed by amination with aromatic amines.
以对甲酚为原料经溴化、水解、甲氧基化和甲基化4步反应合成药物中间体3，4，5-三甲氧基苯甲醛，总收率达53。
The 3,4,5 trimethoxybenzaldehyde is synthesized from p cresol in four steps of bromination, hydrolyzation, methoxylation, and methylation, with an overall yield of 53.
报道了白藜芦醇关键中间体3,5二甲氧基苯甲醛的合成方法。
An improved synthetic method of 3, 5-dimethoxy benzaldehyde which is the key intermediate for synthesizing resveratrol were studied.
起着模板以及还原剂双重功效的聚邻苯二胺载体也可以更换为聚邻甲苯胺以及聚邻甲氧基苯胺空心球、聚苯胺纳米管等。
Other reactive templates can also be used for the preparation of glod nanoparticles supported on polymer, such as poly(o-toluidine) and poly(o-methoxyaniline) hollow microspheres, and PANI nanotubes.
以愈创木酚为起始原料，采用各种不同的催化剂与溴苯缩合制备得到邻甲氧基二苯醚，并研究了碱、催化剂、反应温度、反应时间和加料方式各种因素对该反应的影响。
Methoxydiphenyl ether was synthesized from guaiacol by using various catalysts and bases. The influences of base, catalyst, temperature, time and the way of feeding on the reaction were studied.
采用酶学动力学方法研究2-羟基-4-甲氧基苯甲醛（HMB）对酪氨酸酶的单酚酶和二酚酶活力的抑制效应。
The inhibition effect of 2-hydroxy-4-methoxy-benzaldehyde(HMB)on the activity of monophenolase and diphenolase contained in tyrosinase was studied using enzymological kinetic method.
由对乙酰氧基苯甲酸、对苯二酚二乙酯、2，6-萘二甲酸及间苯二甲酸四种单体通过熔融缩聚反应，合成了全芳香族四组分共聚酯。
The wholly aromatic four-component copolyesters were prepared from p-acetoxy-benzoic acid, hydroquinone diacetate, 2,6-naphthalene dicarboxylic acid and isophthalic acid by melting polycondensation.
前言：目的：改进奥美拉唑中间体2 -硝基- 4 -甲氧基-氨基苯的合成方法。
Objective: To improve the synthesis method of the intermediate of Omeprazole, 2-nitro-4-methoxyl-aminobenzene.
前言：目的：改进奥美拉唑中间体2 -硝基- 4 -甲氧基-氨基苯的合成方法。
Objective: To improve the synthesis method of the intermediate of Omeprazole, 2-nitro-4-methoxyl-aminobenzene.
应用推荐