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1)  benzothiazole [,benzəu'θaiəzəul]
苯并噻唑
1.
Progress in the Synthesis of 2-Substituent-benzothiazoles;
2-取代苯并噻唑的合成进展
2.
Novel electroluminescent polyfluorene containing benzothiazole and pyrazoline;
新型含苯并噻唑及吡唑啉环的聚烷基芴电致发光材料的合成及性能研究
3.
Synthesis and biological activities of benzothiadiazole and benzothiazole derives;
苯并噻二唑类和苯并噻唑类化合物的合成及生物活性
2)  pyrazoline [pi'ræzəli:n]
苯并噻唑
1.
Synthesis of benzothiazoyl-pyrazoline and its fluorescence property;
荧光化合物苯并噻唑基-吡唑啉的合成
2.
Seven new benzothiazolyl pyrazoline compounds were synthesized and their structures determined by IR and fluorescent spectra.
设计和合成了7个新型苯并噻唑基-吡唑啉类化合物,通过元素分析和红外光谱检测,确定了化合物的结构,荧光检测结果表明它们的荧光强度为36。
3.
Synthesis of New Blue Pyrazoline Fluorescent Compounds and Study of Infrared Spectroscopy;
用已合成的苯并噻唑吡唑啉类化合物作为参考[1,2],依据Schellhammer经验中化学结构与荧光性关系,在吡唑啉的1-位引入了苯并噻唑基或苯并咪唑基,3-位引入苯基衍生物,使其具有荧光性,5-位引入苯基作为助色团,可使荧光谱红移。
3)  benzothiadiazole
苯并噻二唑
1.
Synthesis and biological activities of benzothiadiazole and benzothiazole derives;
苯并噻二唑类和苯并噻唑类化合物的合成及生物活性
2.
Theoretical study on the alcoholization mechanism of benzothiadiazole~;
苯并噻二唑醇解反应机理的理论研究
3.
Plant Elicitors of BenzothiadiazoleChu Mingjie Huang Dezhi;
新型植物杀菌剂——苯并噻二唑类植物抗病诱导剂
4)  Benzothiazolyl
苯并噻唑基
1.
Quantum Chemistry Study on Fluorescence Spectra of Five Benzothiazolyl Pyrazoline Compounds;
5种苯并噻唑基吡啉类化合物荧光光谱的量子化学研究
5)  benzothia-zolylhydrazone
苯并噻唑腺
6)  BTH
苯并噻二唑
1.
BTH-induced resistance to Alternaira alternata f. mali in apple;
苯并噻二唑(BTH)对苹果抗斑点落叶病的诱导
2.
The Study of BTH-Induced Resistance to Alternaira alternata f. sp. mali in Apple;
苯并噻二唑(BTH)诱导苹果抗斑点落叶病研究
3.
This article reported the induction, purification and identification of a pathogenesis-related protein from the intercellular fluids of cucumber seedlings, which were treated with benzothiadiazole (BTH) or Pseudoperonospora cubensis.
对苯并噻二唑(BTH)处理和接种霜霉病菌后的黄瓜幼苗叶片胞间隙液中病程相关蛋白的诱导积累及纯化鉴定进行了研究。
补充资料:苯并噻唑
分子式:C7H5NS
分子量:135.18
CAS号:95-16-9

性质:微黄色液体。熔点2℃,沸点231℃,131℃(4.53kPa),相对密度1.2460(20/4℃),折光率1.6379。溶于乙醇、二硫化碳,微溶于水。能随水蒸气挥发。具中性反应,似唑啉气味。

制备方法:由N,N-二甲基苯胺与硫磺反应而得。将N,N-二甲基苯胺和硫磺一起加热回流,反应8h后蒸馏。收集200-260℃馏分,将其溶于浓盐酸中,过滤。向滤液加入硝酸铵水溶液,析出苯并噻唑硝酸盐,过滤后将滤饼溶于水中,加氨水至碱性,析出结晶,过滤干燥后减压蒸馏,收集131℃(4.53kPa)馏分即得成品。

用途:用作照相材料、有机合成中间体,也可用为农业植物资源研究的试剂。

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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