1) 2-Nitrobenzenesulfenyl chloride
邻硝基苯硫氯
2) o-chloronitrobenzene
邻氯硝基苯
1.
Hydrogenation of o-chloronitrobenzene over CNTs Supported Pt Catalyst Obtained by Laser Vaporization of Bulk Metal;
激光溅射法制备Pt/CNTs催化剂用于邻氯硝基苯的液相加氢反应
2.
Effects of supports on catalytic properties of Ni-B amorphous alloy catalyst for liquid-phase hydrogenation of o-chloronitrobenzene;
载体对Ni-B催化剂邻氯硝基苯液相加氢性能的影响
3.
Electrochemical reduction of o-chloronitrobenzene and o-nitrotoulene on Cu-Hg electrode;
邻氯硝基苯和邻硝基甲苯在Cu-Hg电极上的电还原行为
3) o-nitrochlorobenzene
邻硝基氯苯
1.
Determination of o-nitrochlorobenzene by Polarography of β-cyclodextrin- o-nitrochlorobenzene Inclusion Complexation;
β-环糊精-邻硝基氯苯包结物极谱法测定邻硝基氯苯
2.
Catalysis of Co-Cu/ SiO_2 in Oxidative Degradation of Sodium Percarbonate for o-nitrochlorobenzene
Co-Cu/SiO_2催化过碳酸钠氧化降解邻硝基氯苯的研究
3.
1-Hydroxybenzotriazole(Ⅰ) was prepared from o-nitrochlorobenzene.
以邻硝基氯苯为原料先合成1-羟基苯并三唑,再还原为苯并三唑。
4) o nitrochlorobenzene
邻硝基氯苯
1.
Dichlorobenzidine(Ⅳ) was synthesized from o nitrochlorobenzene(Ⅰ) by three step reactions.
以邻硝基氯苯 (Ⅰ)为起始原料 ,经过三步化学反应合成 3,3′ 二氯联苯胺 (Ⅳ ) :Ⅰ在 0 。
2.
The results indicate that the o alkylation of o nitrochlorobenzene in a constant concentration of polyethylene glycol obeys the pseudo first order kinetically.
用不同分子量的聚乙二醇作为相转移催化剂，对邻硝基氯苯的Ｏ－甲基化、Ｏ－乙基化反应进行了研究。
3.
Taking the reaction of O nitrochlorobenzene O methylation by phase transfer catalyst as an example,the mechanism of phase transfer catalysis and kinetics equation are discussed under certain conditions.
以邻硝基氯苯在相转移催化剂作用下Ｏ－甲基化反应为例，在一定条件下探讨了相转移催化机理及动力学方
5) 2-nitrochlorobenzene
邻硝基氯苯
1.
2,2′-Dichlorohydrazobenzene(DHB) was prepared by catalytic hydrogenation of 2-nitrochlorobenzene using Pt/C as a catalyst in alkaline medium.
在碱性介质中,以自制的Pt/C为催化剂,对邻硝基氯苯催化加氢制备2,2′-二氯氢化偶氮苯(DHB)进行研究;采用正交法对加氢还原条件进行了优化,最优条件为反应温度60℃,反应压力0。
2.
o-Nitrophenetole was prepared using phase transfer catalyst by reation of 2-nitrochlorobenzene and ethanol in the presence of sodium hydroxide.
以邻硝基氯苯、氢氧化钠、乙醇为原料,在相转移催化剂的条件下合成了邻硝基苯乙醚。
3.
Nitrodiphenylamine is synthesiized by direct condensing method,adsopting aniline and 2-nitrochlorobenzene as feeds,PEG as phase transfer catalyst.
以苯胺、邻硝基氯苯为原料 ,采用直接缩合法引入相转移催化剂合成邻硝基二苯胺。
6) o-chloronitrobenzene
邻硝基氯苯
1.
Study on Electrochemical Treatment of the O-Chloronitrobenzene Wastewater and Application of HPLC
电化学处理邻硝基氯苯废水的研究及HPLC的应用
2.
Electrochemical Reduction of o-Chloronitrobenzene on Fe-Fe Electrode
邻硝基氯苯在Fe-Fe电极上的电化学行为研究
3.
Ni/TiO_2 catalyst was prepared by an impregnation method and applied in the hydrogenation of o-chloronitrobenzene to 2,2′-dichlorohydrazobenzene.
采用浸渍法制备了Ni/TiO_2催化剂,用于邻硝基氯苯(o-CNB)加氢制备2,2′-二氯氢化偶氮苯(DHB),通过BET,XRD,SEM和活性评价等方法对催化剂的物相结构及催化性能进行了研究,考察了Ni/TiO_2催化剂镍负载量、反应温度、碱用量等工艺条件对催化加氢制备DHB的影响。
补充资料：邻硝基苯硫氯
分子式：C6H4ClNO2S
分子量：189.62
CAS号：7669-54-7
性质：具腐蚀性、易潮解的固体。熔点74.5-75℃。
制备方法：将干燥氯气通入二硫-2,2-二（硝基苯）、四氯化碳和少许碘的混合物中，温度保持在50-60℃。反应液冷至5℃，即结晶析出，得邻硝基苯硫氯，收率61-71%。
用途：肽合成的N-保护基。
分子量：189.62
CAS号：7669-54-7
性质：具腐蚀性、易潮解的固体。熔点74.5-75℃。
制备方法：将干燥氯气通入二硫-2,2-二（硝基苯）、四氯化碳和少许碘的混合物中，温度保持在50-60℃。反应液冷至5℃，即结晶析出，得邻硝基苯硫氯，收率61-71%。
用途：肽合成的N-保护基。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条