邻甲苯胺,o-toluidine
1)o-toluidine邻甲苯胺
1.Chemically oxidative copolymerization of o-toluidine with vinyl acetate;邻甲苯胺与醋酸乙烯酯的化学氧化共聚
2.The electrochemical properties of o-toluidine in 1,2-dichloromethane in the presence and the absence of hydrogen peroxide were investigated at a platinum electrode by cyclic voltammetry.以1,2-二氯乙烷为溶剂,利用循环伏安法研究了邻甲苯胺在铂电极上的电子转移性质,并测试了H2O2存在时邻甲苯胺的循环伏安特性,探讨了电极反应机理。
3.A simple, rapid and sensitive method for the determination o-toluidine and o-nitrotoluene in sample using solid-phase extraction (SPE) and high performance liquid chromatography with ultraviolet detection was developed.建立了以固相萃取技术进行富集 ,高效液相色谱进行分离和检测邻甲苯胺和邻硝基甲苯的方法。
英文短句/例句

1.Improved on process of synthesizing o-cresol by diazotization and hydrolysis of o-toluidine邻甲苯胺重氮化-水解制备邻甲酚工艺改进
2.Contrast test on determination of blood sugar with methods of glucose-oxidase (GOD) and o-toluidine(O-T)葡萄糖氧化酶法与邻甲苯胺法作血糖测定方法对比试验
3.Synthesis of Anthranilic Diamide Derivatives邻甲酰胺基苯甲酰胺类化合物的合成
4.Review on Anthranilic Diamides Insecticides邻甲酰氨基苯甲酰胺类农药研究概述
5.Microwave catalytic synthesis of 2-(benzo[d]thiazol-2-yl)isoindoline-1,3-dione微波催化合成N-(2-苯并噻唑)邻苯二甲酰亚胺
6.Study on Synthesis of N-methyl-4-aminophthalimideN-甲基-4-氨基邻苯二甲酰亚胺的合成研究
7.methyl ortho-benzoylbenzoate邻苯甲酰苯甲酸甲酯
8.Green Synthesis and Structure Characterization of N-o-carboxylphthalimideN-邻羧基苯基邻苯二甲酰亚胺的绿色合成及结构表征
9.Preparation and Electromagnetic Properties of Poly(O/M-Toluidine-Aniline)-Ba Ferrite Composites聚邻/间甲苯胺—苯胺—钡铁氧体复合物的制备及电磁性能研究
10.STUDY OF FLUORESCENCEENHANCEMENT EFFECT OFDYSPROSIUM LANTHANUM o FBA EDA SYSYTEM镝—镧—邻氟苯甲酸—乙二胺体系荧光增敏效应
11.Synthesis of N-phenmethyl phthalimide under Ultrasound Irradiation;超声波辐射下N-苄基邻苯二甲酰亚胺的合成
12.Synthesis of 3,4-Diaminotoluene under Catalytic Hydrogenation and Ordinary Pressure Liquid Phase;常压液相催化氢化制备4-甲基邻苯二胺
13.Study on addition reaction of 2-methoxyaniline upon acrylonitrile promoted by AlCl_3AlCl_3催化邻甲氧基苯胺与丙烯腈加成反应的研究
14.Synthesis of Phthalimido Amide Chiral Molecular Tweezers and Their Optical Properties邻苯二甲酰亚胺酰胺类手性分子钳的合成及其光学性能
15.Synthesis and Biological Activity of Phthalimide-Polyamine Conjugates邻苯二甲酰亚胺-多胺缀合物的合成及其生物活性
16.Preparation and Study of Poly (Aniline-anthranilic Acid) Transition Metal Complex;聚(苯胺—邻氨基苯甲酸)过渡金属络合物的制备及性能研究
17.Synthesis and Preliminary Bioassay of N-Phenylaminophthalimide DerivativesN-苯基氨基邻苯二甲酰亚胺衍生物的合成及初步杀虫活性
18.sulphaloxic acid磺酰苯胺甲酰基苯甲酸
相关短句/例句

o-methylaniline邻甲苯胺
1.3-Methyl-4-acetaminobenzenesulfonyl chloride(Ⅰ) was prepared from o-methylaniline by protecting the amino group and then reacting with chlorosulfonic acid.合成步骤如下:(1)邻甲苯胺、对甲氧基苯胺的氨基保护后,分别与氯磺酸反应得3-甲基-4-乙酰氨基苯磺酰氯(Ⅰ)和2-甲氧基-5-乙酰氨基苯磺酰氯(Ⅴ);(2)对氨基乙酰苯胺(Ⅱ)分别与Ⅰ、Ⅴ在w(CH3COOH)=5%的醋酸中反应,所得缩合物水解得产品Ⅳ、Ⅶ。
2.o-Fluorobenzoic acid was synthesized by Schiemann-reaction of o-methylaniline to give o-fluorotoluene which was oxidized by HNO 3 in an autoclave to abtain the product of 70.以邻甲苯胺为原料 ,经西曼反应合成邻氟甲苯 ,进而经硝酸氧化法得到邻氟苯甲酸 (收率 93。
3)2-Methylaniline邻甲苯胺
4)o-toluidine邻甲基苯胺
1.The resolution was 4 for the separation of the most difficult isomers such as o-toluidine and p-toluidine.该柱对邻甲基苯胺、间甲基苯胺、对甲基苯胺同分异构体显示了很好的色谱分析性能。
2.Indole has been prepared by the reaction of O-toluidine and formic acid to obtain N-formacyl-O-toluidine(O-toluidide),then in the presence of potassium hydroxide by toluone and O-toluidine used as water carrying reagent and solvent converted furter into potassium salt of O-toluidide,followed cyclization and hydrolysis.用邻甲基苯胺和甲酸反应制得N-甲酰基邻甲基苯胺(甲酰化物),然后在氢氧化钾存在下,用甲苯作带水剂,邻甲基苯胺作溶剂制得甲酰化物钾盐,接着环合、水解制得吲哚,其收率达65%。
3.Synthesize saframine O using o-toluidine as primer reactant by diazotization, coupling reaction, reduction reaction, and oxidation.研究了以邻甲基苯胺为起始原料,经重氮化、偶合、还原、氧化反应合成藏花红的方法。
5)o-(p-)toluidine邻(对)甲苯胺
6)o-Tolidine邻联甲苯胺
1.Electrodeposition of the Charge-Transfer Complex Generated during Electrooxidation of o-Tolidine and the Effects of Coexisting Chondroitin Sulfate;邻联甲苯胺电氧化所致电荷转移配合物的电沉积及共存硫酸软骨素的影响
2.In Situ Piezoelectric Infrared Spectroelectrochemistry for Study of Electrochemical Oxidation of o-Tolidine;现场压电红外反射光谱电化学研究邻联甲苯胺的电化学行为
延伸阅读

邻甲苯胺  分子式  CH3C6H4NH2   CAS号  95-53-4  性质  浅黄色易燃液体,暴露在空气和日光中变成红棕色。相对密度0.9984(20/4℃)。熔点-14.7℃。闪点85℃。沸点200.2℃。折射率nD(20℃)1.5725。微溶于水,溶于乙醇和乙醚。能与蒸汽一同挥发。 用途  用作有机合成及染料的中间体   毒性   剧毒。其毒性与苯胺基本相同。吸入蒸气或经皮肤吸收均会引起中毒,生成高铁血红蛋白,引起神经障碍以及致癌等。 工作场所空气中最高容许浓5mg/m3。防护方法参见“苯胺”。  包装储运  采用铁桶包装。贮存于阴凉、通风的仓库内,严禁烟火。按有毒化学品规定贮运。