• 发明提供了(I)新的酰基脲及其多晶型物形式

    The present invention provides novel sulfonylurea salts of a salt of formula (I) and polymorph forms thereof.

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  • 制备酰基衍生物方法,酰基脲衍生物的及其用作农药用途

    Method for producing acyl urea derivatives, salts of said acyl urea derivatives, and the use thereof as pesticides.

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  • 酰基化合物生物活性作用机理常见合成方法进行介绍。

    Biological activities, mechanism of action and commonly synthetic methods of acylurea compounds have been introduced.

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  • 因此酰基类化合物合成应用研究成为农药合成领域的一个热点

    Therefore, synthesis and application of the acylureas have become the hot field of the synthesis of the pesticides.

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  • 本文通过检索文献,对类、酰基类、酰基四唑类化合物生物活性作了系统论述

    By retrieving concerned Literatures, this article discussed comprehensively the biological activities of phenyl ureas, acyl ureas and tetrazoles.

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  • 本文比较全面论述了酰基化合物作用机制、构效关系合成方法安全性以及苯并咪唑类化合物作用机制、安全性和应用情况。

    In the article, we dissertated comprehensively the functional mechanism, the relationship of structure, the synthetical methods and the safety of acylureas and the benzimidazole.

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  • 设计并合成了23酰基化合物,95个双取代类化合物25个双取代硫类化合物。

    Total 23 compounds of Aroyl thiourea scaffold. 95 compounds of bis-substituted urea scaffold, 25 compounds of thiourea scaffold were designed and prepared.

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  • 结果表明,此类磺酰类化合物除草活性苯环5位取代基立体结构电场性质密切相关

    The results show that herbicidal activity is closely related to the steric and electronic properties of the 5-position of the benzene ring.

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  • 酰基二茂铁4-取代氨基反应8相应的缩氨基1~8,它们均属首次制得。

    Propionyl ferrocene reacted with 4-substituted semicarbazides converted into corresponding semicarbazones 1-8, which are not prepared previously.

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  • 目的研究5,5 二苯基乙内酰3 基甲基磷酸钠新的合成工艺。

    Objective To study a new synthesis method of 5,5- diphenylhydantoin-3-ylmethylphosphate disodium.

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  • 本文酰基乙腈1,1,3,3-四甲氧基丙烷为起始原料,经五反应合成得到磺酰除草剂磺隆。

    Sulfonylurea herbicide Rimsulfuron was synthesized by a five-step reaction starting with 2-(ethylsulfonyl)acetonitrile and 1,1,3,3-tetramethoxypropane.

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  • 本文酰基乙腈1,1,3,3-四甲氧基丙烷为起始原料,经五反应合成得到磺酰除草剂磺隆。

    Sulfonylurea herbicide Rimsulfuron was synthesized by a five-step reaction starting with 2-(ethylsulfonyl)acetonitrile and 1,1,3,3-tetramethoxypropane.

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