CAS: 621-40-9; (3-Methylphenyl)Thiourea
该化合物是一种硫尿素衍生物,其成分为甲基代苯组,在有机合成中具有独特的反应性和选择性,其硫尿素作为异环化合物的多用途构件,而3-甲基苯基组则会增强消毒性能和电子特性,影响协调化学的结合性.由于能够形成稳定的复合体,该化合物对于制备药品,农用化学品和金属离子带尤其有用.高纯度和连续性能使它成为研究和工业应用的可靠试剂.在标准条件下,其稳定性确保了处理和储存的便利性.
物理性质
MSDS等安全信息
欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册上下游产品
CAS号4949-87-5 1-benzoyl-3-(3-... | CAS号108-44-1 3-甲基苯胺 | CAS号638-03-9 间甲苯胺盐酸盐 | CAS号621-30-7 间甲苯异硫氰酸酯 | CAS号333-20-0 硫氰酸钾 | CAS号620-51-9 1,3-bis(3-methy... | CAS号60-29-7 乙醚 | CAS号7664-41-7 氨 | CAS号14779-18-1 7-甲基苯并[D]噻唑-2-胺 | CAS号14779-17-0 2-氨基-5-甲基苯并噻唑 | CAS号3085-53-8 3-甲基N-甲酰苯胺 | CAS号108-44-1 3-甲基苯胺 | CAS号63-99-0 3-甲基苯基脲 | CAS号315702-99-9 N-(3-甲基苯基)-4-(4... | CAS号3323-84-0 2-CHLORO-N-(5-M...合成工艺路线路线简述
📜3-甲基苯胺置于ammonium Hydroxide体系中,用 甲醇,丙酮 作为反应溶剂,化学反应生成 间甲苯基-2-硫脲
参考文献:Synthesis And Antitumor Evaluation Of 5-(Benzo[d][1,3]Dioxol-5-Ylmethyl)-4-(Tert-Butyl)-N-Arylthiazol-2-Amines
标题:Synthesis And Antitumor Evaluation Of 5-(Benzo[d][1,3]Dioxol-5-Ylmethyl)-4-(Tert-Butyl)-N-Arylthiazol-2-Amines
摘要:设计靶向化合物作为抗肿瘤药物的策略.
DOI:10.1039/c6Md00234J
海关参考信息
- 2902300000-甲苯
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- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-111808044-A
优先权日:2020-06-30
标 题 :Novel green synthesis method for efficiently synthesizing aminothiazole derivative through carbene insertion/cyclization reaction under catalysis of transition metal
专利号:CN-111808044-B
优先权日:2020-06-30
标 题 :Green synthesis method for efficiently synthesizing aminothiazole derivative through carbene insertion/cyclization reaction under catalysis of transition metal
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:Synthesis Of 2-Aminothiazoles Via Rhodium-Catalyzed Carbenoid Insertion/annulation Of Sulfoxonium Ylides With Thioureas作者:Yuncan Chen,Shan Lv,Ruizhi Lai,Yingying Xu,Xin Huang,Jianglian Li,Guanghui Lv,Yong Wu |发布日期:2021.8
摘要:Sulfoxonium Ylides As Carbene Precursors Couple Smoothly With Thioureas In The Presence Of 5 Mol% Of Rhodium(II) Acetate Dimmer Via Carbenoid Insertion To Afford The Corresponding 2-Aminothiazoles With High Chemoselectivity, Providing A Facile And Efficient Approach To Access A Variety Of 2-Aminothiazole Derivatives With Good Functional Groups Tolerance.
合成参考文献
摘要:Aggarwal, P.; Bebbington, M. W. P., Science of Synthesis Knowledge Updates, (2012) 2, 474.
摘要:National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review., 5(45), 1953
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