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酰氧基

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Calicheamicin can be conjugated to the non-specific antibody using a 4-(4'-acetylphenoxy) butanoic acid or (3-Acetylphenyl) acetic acid linker.

可使用4-(4′-乙酰基苯氧基)丁酸或(3-乙酰基苯基)乙酸连接子使卡奇霉素与所述非特异性抗体共轭结合。

On the base of molecular structure design, the mechanism and technique of the synthesis of 2-(acryloyloxy ethyl trimethyl-ammonium chloride/2-acrylamido-2methylpropane sulfonic acid/acrylamide (AETMAC/AMPS/AM) amphoteric terpolymers by radical co-polymerization in aqueous solution was studied systematically.

依据分子结构设计理论,将2—丙烯酰氧乙基—三甲基氯化铵/2—丙烯酰胺基—2—甲基丙烷磺酸/丙烯酰胺(AETMAC/AMPS/AM)三种单体进行水溶液自由基共聚,合成了AP系列两性离子聚合物。

From 3-chloropropene bycondensation with sodium ethylate in ethanol to form 3-ethoxypropene followed by anti-Markovnikov addition with HBr inthe presence of benzoyl peroxide.

3-氯丙烯与乙醇钠在乙醇中回流制得3-乙氧基丙烯,继而在过氧苯甲酰存在下,与溴化氢经反马氏加成制得1-溴-3-乙氧基丙烷,总收率89。

From Cacalia deltophylla (collected from Luqu County, Gansu Province), 22 compounds were isolated, of which 15 compounds have been identified. Among them, two compounds are new. They are named as 3-methyl-4-hydro-8-acetyl-furanonaphth-9-one and 1hydroxy-2-methoxy-3-acetyl-4, 8-dimethyl-5, 8-dihydro-naphthalene.

从采自甘肃省碌曲县的三角叶蟹甲草全草的甲醇提取物的石油醚部分和乙酸乙酯部分中,采用同样方法分离得到22个化合物,鉴定了其中的15个化合物,其中有2个为新化合物,分别命名为3-甲基-4-氢-8-乙酰基-呋喃萘-9-酮(2)和1-羟基-2-甲氧基-3-乙酰基-4,8-二甲基-5,8-二氢-萘(3)。

Objective:To establish a RP-HPLC method to quantify a new chemical entity HZ08N-cyano-1-[(3,4-dimethoxyphenylmethyl]-3,4-dihydro-6,7-dimethoxy-N -octyl-2(1H)-isoquinoline carboximidamideand its related substances.

目的:建立HZ08N-腈基-1-[(3,4-二甲氧基苯基甲基]-3,4-二氢-6,7-二甲氧基-N-辛基-2(1H)-异喹啉碳酰亚胺的含量测定及有关物质检查方法。

The compound of BNTMBP wassynthesized by the condensation reaction between 4-chloronitrobenzene (4CNB) and 4, 4'-dihydroxy-3, 3', 5, 5'-tetramethyl biphenyl in the presence of potassium carbonate in the mixture solvents of N, N-dimethylformamide and tolune.

4, 4'-二羟基-3, 3', 5, 5'-四甲基联苯、4-氯硝基苯(4CNB)和碳酸钾在N, N-二甲基甲酰胺和甲苯的混合溶剂体系中回流反应,合成得到了4, 4'-双(4-硝基苯氧基)-3, 3', 5, 5'-四甲基联苯;随后,在Pd/C-水合肼的还原体系中,被进一步还原,得到了4, 4'-双(4-氨基苯氧基)-3, 3', 5, 5'-四甲基联苯。

Methods 2-(piperazin-1-yl)-1-(pyrrolidin-1-yl)ethanone (2) was synthesized from pyrrolidine via amidation and substitution, followed by treating with chloroacetyl chloride and triphenylphosphine in a "one pot" manner to give the corresponding phosphonium chloride 3 in a stable and pure form after crystallization from isopropanol.

以四氢吡咯为原料,先与氯乙酰氯成酰胺,再与哌嗪发生取代反应制得中间体[(1-四氢吡咯基)甲基]哌嗪(2);化合物2与氯乙酰氯和三苯基膦反应,经异丙醇重结晶得到稳定的有机鏻盐(3);化合物3与3,4,5-三甲氧基苯甲醛发生Wittig反应,再与马来酸成盐得目标化合物马来酸桂哌齐特(1)。

Synthesis and structural characterization of novel cycioplatinated complexes with 2-aryl imidazolines 2-arylimidazoline ligands 2a-2d were synthesized from benzoyl chloride or p-methoxybenzoyl chloride with aminoethanol or valinol and 2e was synthesized from 2-phenylimidazoline.

新型2-芳基咪唑啉环铂化合物的合成与结构表征以苯甲酰氯或4-甲氧基苯甲酰氯和氨基醇(2-氨基乙醇或外消旋的缬氨基醇)为原料,合成了四种2-芳基咪唑啉配体2a-2d,以2-苯基咪唑啉为原料合成了配体2e,其中2d为新化合物。

The results showed 3 types of aluminum compound prepared in this paper all had good poison protection effectiveness on such impurities as stannous chloride,lead oxide,sodium hydrogen sulfate,and so on.Moreover,the mechanism of the poison of catalyst was also discussed.

结果表明,合成的3种防中毒剂即防-1、防-2(主要成分为乙酰丙酮合铝)及防-3(主要成分为二乙酰丙酮基异丙氧基铝)对二月桂酸二丁基锡、氯化亚锡、二正丁胺、硫脲、氧化铅及硫酸氢钠等杂质均有较好的防中毒作用;不同防中毒剂对不同杂质的防中毒作用有一定的选择性。

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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