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1)  thiazolidin-4-one
噻唑烷-4-酮
1.
Microwave Assisted Synthesis and Antibacterial Study of 3-Naphthyl-2-[(un)substituted phenyl]-1,3-thiazolidin-4-ones;
新型3-萘基-1,3-噻唑烷-4-酮衍生物的微波促进合成及其抗菌活性研究
2.
Microwave Assisted Synthesis and Antifungal, Anti-tumor Study of 2-(2,6-Dichlorophenyl)-1,3-thiazolidin-4-ones
2-(2,6-二氯苯基)-1,3-噻唑烷-4-酮衍生物的微波促进合成及抗真菌、抗肿瘤活性研究
2)  4-thiazolidone
4-噻唑烷酮
1.
3-Substituted-2-acylimino-4-thiazolidones were synthesized by reaction of N-substituted-N'-benzoyl (or acetyl) ureas with haloacetic acid or ethyl α-bromoacetate and its 5-acetic acid compounds were obtained by reaction of N-aryl-N'-benzoyl ureas with maleic anhydride.
通过N-烃基-N′-酰基硫脲和卤代乙酸(或卤代乙酸酯)反应,合成了一些新的3-取代-2-酰亚胺-4-噻唑烷酮类化合物,并对反应机理作了探讨。
3)  4-oxo-thiazolidine
4-羰基噻唑烷酮
4)  thiazolidinone
噻唑-4-酮
1.
Synthesis and Insecticidal Activities of N-Carbonylamido-2-(4-oxo- 4H-1-benzopyran-3-yl)-4-thiazolidinones Derivatives by Microwave-Assisted Parallel Syntheses;
微波辅助下N-酰胺基-2-(4-氧代-4H-色烯-3-基)噻唑-4-酮类衍生物的平行合成及其杀虫活性
5)  thiazolidone
噻唑烷酮
1.
Five N tetrahydrobenzothiazolyl imines have been synthesized by the condensation of 4,5,6,7 tetrahydro 2 benzothiazolamine with aromatic aldehydes and the reactions of imines respectively, with thioglycollic acid obtained five thiazolidones.
2-氨基四氢苯并噻唑和芳香醛进行缩合反应,合成了5个N-四氢苯并噻唑亚胺化合物,它们分别与巯基乙酸反应制备了5个4-噻唑烷酮。
2.
According to the principle of superposition activity, in this article, we have synthesized a series of thiazolidone and acylthiourea derivatives which are not reported in the literature by introducting 1,2,3-triazole-based, 1,3,4–thiadiazole and dibenzo into acetyl-hydroxy acyl thiazolidoneand thiourea derivatives through the promotion of ultrasonic radiation.
噻唑烷酮类化合物具有重要生理活性,可作杀菌剂、放射线增感剂、抗高血压和糖尿病的药物。
6)  2,4-thiazolidinedione, 2-thio- [qr]
2-硫代-4-噻唑烷酮
补充资料:(RS)-3-(仲丁基硫基(乙氧基)膦酸)-1,3-噻唑烷-2-酮
分子式:C9H16NO3PS2
分子量:283.3
CAS号:

沸点:198℃(66.66Pa)℃
蒸气压:大于5.6E-4Pa(25℃)
毒性LD50(mg/kg):大鼠急性经口LD50为:雄73、雌57,大鼠急性经皮:雄2396、雌861。本品对免眼陌有刺激,而对皮肤无刺激。
性状:纯品为浅棕色油状物
溶解情况:溶解度(20℃,mg/L)水9.85,正己烷15.14。
用途:有机磷杀线虫剂。主耍用干防治线虫、蚜虫等。
制备或来源:1-氢基-2-乙基硫酸酯与二硫化碳和氢氧化钾的水溶液在乙醇中反应,生成2-噻唑烷硫酮,该化合物用过氧化氢在甲醇中于室温下氧化,生成2-噻唑烷酮,再用丁基锂在四氢呋喃中锂化,然后与磷酰氯在室温下反应3h,即制得产品。
类别:杀虫剂


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