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1)  trichloroacetyl chloride
三氯乙酰氯
1.
This paper introduces the methods of preparation of 3,5,6-trichloropyridin-2-ol, and mainly discusses the preparation from trichloroacetyl chloride and acrylonitrile by separately conducting the individual addition, cyclization and aromatization steps.
介绍了农药中间体3,5,6-三氯吡啶-2-醇钠的合成路线和合成方法,并详细讨论了在催化剂条件下用三氯乙酰氯和丙烯腈三步法合成三氯吡啶醇钠的方法。
2.
The outlets of methane tetrachloride produced in the production facilities of chloromethane in China at present were proposed,such as conversion to diphenyl ketone,ethylene tetrachloride,cinnamic acid,trichloroacetyl chloride,methane chloride and chloroform.
提出了目前我国氯甲烷生产装置副产的四氯化碳的出路:转化成二苯甲酮、四氯乙烯、肉桂酸、三氯乙酰氯、一氯甲烷、氯仿。
3.
Thus,91 0 g trichloroacetyl chloride and 34 5 g acrylonitrile were refluxed with 1 4 g catalyst C D in 200 mL nitrobenzene at 145 ℃ for 4 h and.
三氯乙酰氯和丙烯腈在催化剂CD 存在下 ,以硝基苯作溶剂 ,回流下连续完成加成与环化 ,再芳构化 ,得 3,5 ,6 三氯吡啶 2 酚或其钠盐。
2)  trichloroacetic chloride
三氯乙酰氯
1.
A by-product which will result in unfavorable effects for production technology is usually formed in the process of synthesizing trichloroacetic chloride.
三氯乙酰氯生产过程中,有一种对生产工艺有不良影响的副产物,通过对副产物进行气质的分析,解决了工艺中的实际问题,并用气质联用仪进行了表征。
2.
Fenchlorazole ethyl was synthesized in the suitable solvent at 115℃ with α amino (2,4 dichlorophenylhydrono) glyoxylic ethyl ester and trichloroacetic chloride (molar ratio 1∶1) as the raw materials.
以α 氨基 (2 ,4 二氯苯基亚联氨基 )乙醛酸乙酯和三氯乙酰氯为原料合成解草唑 ,选用合适的溶剂 ,将酰化、合环一步完成 ,提高了收率 ,简化了操作 ,优惠摩尔比为 1∶1 。
3.
Three possible processes to synthesize trichloroacetic chloride was evaluated based on the yield,cost,waste treatment, equipment and operation.
本文介绍了三氯乙酰氯的合成方法及其在农药合成中的应用。
3)  trichloro-acetic chloride
三氯乙酰氯
1.
Synthesis of trichloro-acetic chloride and its application;
三氯乙酰氯的合成与应用
4)  chloracetamic acid
三氯乙酰胺氯
5)  trichloroacetamide [,trai,klɔ:rə,ə'setəmaid]
三氯乙酰胺
1.
Synthesis of New Urea Compounds from Nsubstituted Trichloroacetamides and Biological Activities Study .Synthesis of (1Furoyl4aryl)hydrazinecarboxyamide;
N-取代三氯乙酰胺合成新脲类化合物及其生物活性的研究 Ⅳ.1-呋喃酰基-4-芳基氨基脲的合成
2.
Eight 2-benzoyl-N-arylhydrazinecarboxamides (PhCONHNHCONHAr) (Ar=2-ClC 6H 4, 3-ClC 6H 4, 4-ClC 6H 4, 3,4-Cl 2C 6H 3, 2-MeC 6H 4, 3-MeC 6H 4, 4-MeC 6H 4, 2,4-Me 2C 6H 3) have been synthesized via the reaction of N-substituted trichloroacetamides with benzoylhydrazine mediated by NaOH and characterized by elemental analyses, 1H NMR and IR spectra.
以N 取代三氯乙酰胺在碱催化下与苯甲酰肼反应 ,合成了 8种 2 苯甲酰基 N 芳基氨基脲 3a~ 3h ,其结构经元素分析、IR和1HNMR所表征 ;初步生物活性测定表明 ,部分化合物对大肠杆菌、枯草杆菌和金黄色葡萄球菌具有一定的抑菌活性 。
6)  Trifluoroacety l chloride
三氟乙酰氯
补充资料:三氯乙酰氯
分子式:C2HCl4O
分子量:181.83
CAS号:76-02-8

性质:无色有刺激性气味液体。沸点114-116℃,相对密度1.541-1.543(20)。遇水、醇分解,并放出大量的氯化氢

制备方法:暂无

用途:广泛用于合成广谱,高效杀虫、杀螨剂毒死蜱,甲基毒死蜱和除草剂的重要中间体。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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