1)  1-Chloro-2-(trifluoromethyl)benzene
邻氯三氟甲基苯
2)  o-Chloro-α,α,α,-trifluorotoluene
邻氯三氟甲基苯
3)  2-Chlorobenzotrifluoride
邻氯三氟甲基苯
4)  o-chlorophenol
邻氯酚
1.
Study on microwave-assisted regeneration of hypercrosslinked polymeric adsorbent adsorbing o-chlorophenol;
吸附邻氯酚的超高交联树脂微波辅助再生研究
2.
Sorption properties of phenol,o-chlorophenol,2,4-dichlorophenol on four kinds of suspended particles sampled from Changjiang Estuary and Hangzhou Bay were investigated.
研究了4种分别取自长江口和杭州湾的悬浮泥沙样品对苯酚、邻氯酚和2,4-二氯酚的吸附特性。
5)  o-chlorobenzyl chloride
邻氯氯苄
1.
The preparation of o-chlorobenzaldehyde from the residual liquid generated in the production of o-chlorobenzyl chloride;
由生产邻氯氯苄的残液制备邻氯苯甲醛
2.
According to the main problem of current synthesis of o-chlorobenzyl chloride in our country,effective improvement was studied to increase the reaction conversion to 60% by use of a new catalyst CHJ-3.
针对目前国内邻氯氯苄生产工艺存在的主要问题,通过选用新型催化剂CHJ-3,改进催化氯化工艺,使氯化反应邻氯甲苯转化率达到60%。
3.
Taking o-cholorotoluene as raw material,the factors influencing the photochlorination synthesis of the o-chlorobenzyl chloride were investigated.
研究了邻氯甲苯光氯化生成邻氯氯苄的各项影响因素,在适宜条件下,邻氯甲苯的转化率可达75%以上,反应过程邻氯氯苄的收率可达90%。
6)  o-chloroaniline
邻氯苯胺
1.
MOCA is prepared with o-chloroaniline and paraformaldehyde as materials.
以邻氯苯胺和多聚甲醛为反应原料制备MOCA。
2.
The cheap available starting material,O-chloroaniline,reacted with trichloroacetaldehyde monohydrate and hydroxylamine hydrochloride to produe N-(2-chlorophenyl)-2-(hydroxyimino) acetamide;which was treated with concentrated sulfuric acid to obtained 3-chlorolisatin,then 3-chlorolisatin was oxidized by hydrogen peroxide to afford 2-amino-3-chlorobenzoic acid.
以邻氯苯胺为原料,与水合三氯乙醛、盐酸羟胺反应先制得邻氯基(N-肟基乙酰)苯胺,用浓硫酸关环生成3-氯靛红。
3.
A series of titania-supported nickel catalysts with different Ni loadings (10%~40%) were prepared by the incipient impregnation method and applied in the hydrogenation of o-chloronitrobenzene to o-chloroaniline.
用等体积浸渍法制备了一系列不同镍负载量的负载型Ni/TiO2催化剂,并将其应用于邻氯硝基苯加氢制邻氯苯胺的反应。
参考词条
补充资料:邻氯三氟甲基苯
分子式:C7H4ClF3
分子量:180.56
CAS号:88-16-4

性质:无色透明液体。熔点7.0℃,沸点152.1℃,相对密度1.373,折射率1.4554,闪点44℃。易燃(152℃自燃)。不溶于水,易溶于乙醇、乙醚。

制备方法:以邻氯甲苯为原料,经侧链光氯化,得邻氯三氯甲基苯;根据所用催化剂不同,有两种氟化方法。1.五氯化锑催化氟化法。2.三氯化磷催化氟化法。每生产1t产品原料消耗分别为:邻氯甲苯1100kg,氯气2000kg,氟化氢520kg。

用途:本品用于医药、农药等精细有机化工产品的合成。五氟利多的中间体。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。