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1)  2-thiazolidinone
2-噻唑烷酮
1.
Fosthiazate was synthesized by condensing 2-thiazolidinone with O,O'-diethylthio- phosphonochloride,and then alkylating the resulting O,O'- diethyl-2-oxo-1,3-thiazolidine-3-thiophosphate with dimethylamine, followedby direct alkylation of the ammonium salt with 2-bromobutane.
先将2-噻唑烷酮与O,O'-二乙基硫代磷酰氯进行缩合反应生成O,O'-二乙基-2-氧代-1,3-噻唑烷-3-基硫逐磷酸酯,该硫逐磷酸酯再与二甲胺反应生成相应硫代磷酸酯铵盐,然后与溴代仲丁烷进行烷基化反应得到噻唑磷。
2.
Fosthiazate was synthesized by reacting phosphorus trichloride with S-sec-butyl disulfide and then condensing with 2-thiazolidinone.
介绍了以三氯化磷、仲丁基二硫化物为原料反应得到O-乙基-S-仲丁基硫代磷酰氯,再与2-噻唑烷酮缩合得到噻唑磷的合成方法。
3.
Its yield of 2-thiazolidinone came up to 82%.
以2-噻唑硫酮为原料,双氧水为氧化剂,醇钠为催化剂,合成2-噻唑烷酮
2)  2-thiazolidinethione
2-噻唑烷酮
1.
2-Thiazolidinone was synthesized by the exchange reaction between the oxygen of chloroethanol and sulphur atom of 2-thiazolidinethione.
2-噻唑烷酮不仅是一个有用的中间体,而且其本身也具有一定的杀菌活性。
2.
Thiazolidone is synthesized by 2-thiazolidinethione and hydrogen peroxide.
本文以2-噻唑硫酮为原料,双氧水为氧化剂,对2-噻唑烷酮的合成进行了探索性研究,并将其工艺条件进一步优化,使反应收率达60%。
3)  thiazolidine-2-thione
噻唑烷-2-硫酮
4)  Tetrahydrothiazolyl thione
2-噻唑烷硫酮
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-Thioxo-2,4-thiazolidindione
2-硫代-2,4-噻唑烷二酮
补充资料:噻唑烷
分子式:
CAS号:

性质: 又称四氢噻唑(tetrahydrothiazole)。沸点164~165℃;相对密度1.131;折射率1.5508。溶于水、乙醇、乙醚及丙酮。与盐酸形成的盐熔点180℃(分解)。能与乙酸酐或乙酰氯进行乙酰化,其N-乙酰基衍生物沸点83~85℃(93Pa),由β-巯基乙胺与甲醛反应制取。

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