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1)  benzyl chloride
苄氯
1.
Polymerization of styrene initiated with copper(Ⅰ) chloride/ethylenediamine/benzyl chloride was investigated.
研究了以氯化亚铜/乙二胺/苄氯体系引发苯乙烯聚合反应,可以得到数均分子量高达2。
2.
Benzyl propionate was synthesized by esterification of benzyl chloride with propionic acid in the presence of a new polystyrene diethanol amine resin.
应用聚苯乙烯二乙醇胺树脂 (PSDEA)催化苄氯与丙酸的酯化反应 ,合成了丙酸苄酯 。
3.
The mechanism of C C coupling reaction from benzyl chloride with Au(Ⅰ) phosphine bridge complex as photocatalyst was explored.
我们已发现,金(Ⅰ)和铜(Ⅰ)的膦桥双核配合物[Au2(μdppm)2]2+,[Cu2(μdppm)2(CH3CN)4]2+和[Au2(μdmpm)3]2+(dppm=双二苯基膦甲烷,即Ph2PCH2PPh2;dmpm=双二甲基膦甲烷,即Me2PCH2PMe2)对苄氯的碳碳偶联反应[4]2PhCH2ClPhCH2CH2Ph具有较高的光催化活性,并用多种手段研究了[Au2(μdppm)2]2+对此反应的催化机理。
2)  benzyl chloride
氯苄
1.
The influence of K_2CO_3 on the double carbonylation of benzyl chloride was investigated.
探讨了碳酸钾对氯苄双羰化反应的影响,发现氯化钴/碳酸钾对氯苄的双羰化反应有一定的助催化作用。
2.
1-(4-Aminophenylmethanesulfonyl)pyrrolidine(Ⅰ) was prepared starting from benzyl chloride in total yield of 32.
以氯苄为主要原料制备了对氨基苯甲磺酰吡咯烷(Ⅰ)。
3.
1-(4-Nitrophenyl methanesulfonyl) pyrrolidine (Ⅴ) was prepared by four-step reactions, starting from benzyl chloride (Ⅰ).
以氯苄为原料,经4步反应制得p-硝基苯甲磺酰吡咯烷。
3)  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%。
4)  2-chlorobenzyl chloride
邻氯氯苄
1.
A gas chromatography with n-tridencame as the internal strandard was used for determing the content of industrial 2-chlorobenzyl chloride.
采用气相色谱内标法,以正十三烷作内标物,测定工业邻氯氯苄的含量。
2.
According to the key problems of current domestic synthesis process of 2-Chlorobenzyl Chloride, effective improvement had been studied by applying advanced reaction rectification technology to increase the reaction conversion to 78%; Therefore, the production cost was reduced.
针对目前国内邻氯氯苄生产工艺存在的主要问题,通过采用先进的反应精馏技术,改进氯化合成工艺,将反应转化率提高到78%,从而有效地降低了生产成本,经济效益和社会效益显著,具有很好推广应用前景。
5)  4-chlorobenzyl chloride
对氯氯苄
1.
The influence of reaction temperature,the molar ratio of trimethyl phosphite to 4-chlorobenzyl chloride,reaction time and feeding mode on the yield of p-chlorobenzyl phosphate was investigated.
以亚磷酸三甲酯和对氯氯苄为原料,通过Arbuzov重排反应制得了对氯苄基磷酸酯。
2.
p-chlorobenzyl) pyridine is prepared from 4-chlorobenzyl chloride and pyridine hydrochloride via condensation.
以对氯氯苄与盐酸吡啶缩合法制备 2 -对氯苄基吡啶 。
6)  dichlorobenzyl chloride
二氯氯苄
补充资料:2,4,5-三氟苄氯
CAS:88419-56-1
分子式:C7H2ClF3O
分子质量:194.54
沸点:77℃

中文名称: 2,4,5-三氟苄氯;2,4,5-三氟苯甲酰氯

英文名称: 2,4,5-trifluorobenzoyl chloride
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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