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二苯酰

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Pomalidomide is a new IMiD with high in vitro potency.

3-氨基-N-(2,6-二氧代-3-哌啶基)邻苯二甲酰亚胺是一种体外高效力的新型IMiD。

As CAAX-mimetics, 1, 3-dihydro-5-phenyl-2-H-1, 4-benzodiazepin-2-one was modified by linking carboxyl groups with various carbon through N-1 and C-3, 3-(imidazol-4-yl) propion amido group with different substituents was connected at C-7; In the synthesis of bisubstrate analogues, thiocarbamido compounds was alkylated by alkyl iodide and then hydrolyzed to give alkylthiol benzoate compounds.

1,4-苯并二氮杂草-2-酮类化合物的合成过程中分别对其1、3、4和7位进行了基团变化,在1和3位连接不同长度含羧基或酯基的侧链,在7位连接不同取代的咪唑丙酰氨基。在苯甲酸硫醇酯化合物合成过程中,建立了一种硫原子连有不同长度碳链的苯甲酸硫醇酯的合成方法。

Objective To establish a HPLC method for the determination of aceclofenac in human plasma.Methods Acidified samples of plasma (500μL) were extracted with 4 mL of ethyl acetate. The organic phase was evaporated to dryness by nitrogen at 40℃ water bath. The residue was redissolved in mobile phase and then was determined.

醋氯芬酸是一种具有镇痛作用的非甾体类抗炎药物[1],化学名为[邻-(2,6-二氯苯基)氨基]苯乙酰乙酸,l992年首先于西班牙上市,具有明显广泛的抗炎作用和强力的解热镇痛作用,其生物半衰期较双氯芬酸长,胃肠耐受性较双氯芬酸好,抗炎活性优于萘普生和保泰松[2]。

Under catalysis of AlCl3, trans-1-chloro-3-phenyl-1-propen-3-one was first prepared using benzoyl chloride and acetylene in CH2Cl2 at 20~25℃, which the yield is 7% higher than that in CCl4 at 40~45℃.

通过对其反应条件的研究,首次用苯甲酰氯和乙炔在三氯化铝作用下合成出反-3-苯基-1-氯-1-丙烯-3-酮;并发现用二氯甲烷作介质在20~25℃下的反应产率,比用四氯化碳作介质在40~45℃下的反应产率约高7%。

A novel type of photoalignment material based on the esterification reaction of 3,5-dihydroxyl benzyl alcohol and cinnamoyl chloride was firstly reported in this paper. The distinct property of this material is the nonlinear branch conformation and its polarity end with hydroxyl group.

通过在3,5-二羟基苯甲醇分子中的双酚基基团上引入双肉桂酰酯光敏基团的酯化反应,合成了一类新型的分子顶部为羟基极性基团,整个分子构型类似于树枝状的光敏小分子化合物。

Using phenol and benzyl chloride as raw materials and N,N-dimethyl formamide as solvent, benzyl phenyl ether was synthesized under microwave radiation.

采用微波辐射技术,以苯酚、氢氧化钾和氯化苄为原料,N,N-二甲基甲酰胺为溶剂合成了苄苯醚。

A new monomer,4-hexanoxyl-4′-undecylene-[10]-acyloxyazobenzene was synthesized using the main materials:phenol,underlenic acid,1-bromo- n -hexane, p -nitrophenol,thionyl chloride,by the substitution,reduction,couping and diazotization methods.A new polymer was prepared by hydrosilation reaction of poly (methylhy-drosiloxane) with the monomer.

以苯酚、十一烯酸、正溴己烷、对硝基苯酚和二氯亚砜为主要原料,通过取代、还原、重氮化和偶合等反应,合成了一种新的液晶单体 4-己氧基-4′-十一烯-[10]-酰氧基偶氮苯,并与聚通过硅氢加成生成一种新的高分子液晶。

In the first part of this thesis, a formal [4+2] cycloaddition of ketenes with N-benzoyldiazenes catalyzed by chiral NHCs was studied, which gave 1,3,4-oxadiazin-6-ones in very high yields and enantioselectivites.

论文的第一部分内容是在手性氮杂环卡宾的催化下,烯酮与N-苯甲酰偶氮化合物的环加成反应,合成各种手性的噁二嗪酮,它们还可以经过简单的两步一锅法制备手性氨基酯。

To synthesize aryl pyrimidines by taking benzene, methyl benzene ,acetic ether,1,2-dichloroethane as solvent,the yield and purity of the product are high by taking methyl benzene as solvent.

分别选用苯、甲苯、乙酸乙酯、二氯乙烷作为溶剂合成桂皮酰哌啶,结果表明甲苯作为溶剂时产品纯度高,收率高,可用于大规模生产。

A process for synthesis of-2-{[4-(3-methoxypropoxy)-3-methyl-pyridin-2-yl]methyl- sulfinyl}-1H-benzimidazole from 2,3-lutidine was studied.

以2,3-二甲基吡啶为起始原料,经过11步反应,不对称合成了质子泵抑制剂的关键中间体:-2-{[4-(3-甲氧基丙氧基)-3-甲基吡啶-2-基]甲基亚硫酰基}-1H-苯并咪唑。

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Since this year, in a lot of villages of Beijing, TV of elevator liquid crystal was removed.

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