2-噻唑烷酮,2-thiazolidinone
1)2-thiazolidinone2-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
英文短句/例句

1.The Synthesis Research and Process Design of 2-thiazolidinone, as Intermediate for Fosthiazate新型杀线虫剂噻唑磷的关键中间体2-噻唑烷酮的合成研究与工艺设计
2.Review of the therapeutic effect of thiazolidine treating for diabetes mellitus typeⅡ噻唑烷二酮类药物治疗2型糖尿病的效果
3.SYNTHESIS OF 3-SUBSTITUTED-2-ACYLIMINO-4-THIAZOLIDONES AND ITS 5-ACETIC ACID COMPOUNDS3-取代-2-酰亚胺-4-噻唑烷酮及其5-乙酸化合物的合成
4.Microwave Assisted Synthesis and Biological Activity of 2-(Hydroxymethyl)-3-aryl-1,3-thiazolidin-4-ones2-羟甲基-3-芳基-1,3-噻唑烷-4-酮衍生物的微波促进合成及生物活性
5.Synthesis of 2-dodecyldithio-4-phenyl-1,3,4-thiadia-zole-5-thione and study on inhibiting corrosion2-十二烷基二硫代-4-苯基-1,3,4-噻二唑-5-硫酮的合成及抗腐蚀研究
6.Protective effect of thiazolidinediones on the kidney噻唑烷二酮类药物对肾脏的保护作用
7.Synthesis of Triazole Thiazolinone Derivatives Containing 1,2,3-Triazoleyl under the Ultrasonic Radiation超声辐射下含1,2,3-三唑噻唑烷酮衍生物的合成
8.Improvement in synthesis of 1-(thiophen-2-yl)hexadecan-1-one2-十六烷基噻吩酮的合成工艺改进
9.Design, Synthesis and Screening of Thiazolidinone Derivatives抗非小细胞肺癌的2-芳亚胺基-4-噻唑烷酮化合物库的设计、合成与生物活性筛选
10.Effects of Thiagolidinediones on C-reactive protein and fibrinogen in the patients with type 2 diabetes mellitus accompanied by metabolic syndrome噻唑烷二酮对2型糖尿病的代谢综合征患者C反应蛋白、纤维蛋白原的影响
11.Synthesis of a New Penetration Enhancer N-alkylbenzisothiazolone;新型促渗剂N-正烷基苯并异噻唑酮的合成
12.The Synthesis of Novel Thiazolidone and Acylthiourea Derivatives新型噻唑烷酮和酰基硫脲衍生物的合成
13.Design, Synthesis and Antiviral Evaluation of Novel 2,3-Diaryl-1,3-Thiazolidin-4-One Derivatives as HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors新型噻唑烷酮类HIV-1 NNRTIs的设计、合成及活性研究
14.The Clinical Value of Thiazolidinediones in Type 1 Diabetes噻唑烷二酮类药物在1型糖尿病治疗中的价值
15.A Systematic Review of Thiazolidinedioes for Metabolic Syndrome噻唑烷二酮类药物治疗代谢综合征的系统评价
16.Study on The Synthetic Method of 5-Alkyl-2-amino-1,3,4- thiodiazoles.;2-氨基-5-烷基-1,3,4-噻二唑类化合物合成方法研究
17.Synthesis of 2-Alkylamino-thieno[2,3-d] pyrimidin-4(3H)-ones;2-烷氨基噻吩并[2,3-d]嘧啶-4(3H)-酮的合成
18.Study on the Structure-Activity Relationships and Synergism of Diverse Thiazolidinedione Molecular Probes in Compound Mixtures;混合物中多种噻唑烷酮类小分子探针的构效关系及协同作用研究
相关短句/例句

2-thiazolidinethione2-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 thione2-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-thiazolidindione2-硫代-2,4-噻唑烷二酮
延伸阅读

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。