• 采用催化合成合成了4 氯苯甲酸纤维素酯;

    The cellulose tris(4-chlorobenzoate) has been synthesised by the catalytic method and was supported on Gas Chrom Q.

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  • 该法邻、间、对-氯苯甲酸混合物进行测定,结果良好

    The mixtures of o-, m-, p-chlorobenzoic acid are analyzed and the results are satisfactory.

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  • 分离混合、对氯甲苯氧化制得混合邻、对氯苯甲酸

    Chlorobenzoic acids can be synthesized by oxidation of mixed chlorotoluene which was difficult to separate.

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  • 氯化亚砜滴氯苯甲酸乙醇混合物中,反应生成氯苯甲酸乙酯。

    Thionylchloride was added to a solution consisting of ethanol and o-chlorobenzoic acid to affore o-chlorobenzoic ester.

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  • 氯苯甲酸-2,4,6-三吡啶基三嗪稀土配合物合成表征发光性能

    Synthesis, Characterization and Fluorescence Properties of Rare Earth with p-Chloro-benzoic Acid and 2,4,6-Tris-(2-pyridyl)-s-triazine.

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  • 本文在研究甲苯混合氧化合成氯苯甲酸工艺时,采用氧气液相催化氧化反应压力为常压。

    The method of liquid oxygen oxidation of chlorotoluene mixture was choosen to synthesize chlorobenzoic acids, and the reactions were carried out under atmospheric pressure.

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  • 低毒高效、机理独特新型四嗪类杀剂。叙述了2-氯苯甲酸起始原料合成氟螨嗪的方法。

    Flufenzine was a new kind of acaricide which had low toxicity, high activity and special mode of action. Fluenzine was prepared by using 2-chlorobenzoic acid as start material.

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  • 本文考察萃取浓度用量、反应温度分散用水量等因素对对氯苯甲酸离解萃取过程影响,得到了最佳的分离工艺条件。

    In this study, base and acid were used for extraction, and the amount and concentration of extraction, temperature and the amount of water as scatter were investigated during the process oft...

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  • 3,5— 二氯苯甲酸作为物,采用液相色谱(HPLC)法同时测定了百甲合剂水剂中的两种有效成份百草敌和二甲四氯

    In this paper, 3,5-Diclorobenzic acid was used as the internal standard to determinate the effective costituces in banvel·NH(CH3)2-MCPA·Na solution by HPLC.

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  • 本文主要报道以2- 氨基-4, 6-二羟基嘧啶氯苯甲酸起始原料合成除草剂磺隆,以及详细地介绍了各个中间体的合成方法

    This paper reports the synthesis of herbicide ofprimisulfuron-methyl, the method uses 2-amino-4,6-dihydroxylpyrimidine and O-chlorobenzoic acid as the raw materials.

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  • 本文主要报道以2- 氨基-4, 6-二羟基嘧啶氯苯甲酸起始原料合成除草剂磺隆,以及详细地介绍了各个中间体的合成方法

    This paper reports the synthesis of herbicide ofprimisulfuron-methyl, the method uses 2-amino-4,6-dihydroxylpyrimidine and O-chlorobenzoic acid as the raw materials.

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