- 英文名称2,3,4,5-Tetrachlorobenzoic Acid
- 中文名称2,3,4,5-四氯苯甲酸
- IUPAC名称2,3,4,5-tetrachlorobenzoic acid
- 其它别名2,3,4,5-四氯安息香酸; 2,3,4,5-Tetrachloro Benzoic Acid
- CAS编号50-74-8
- MFCD编号:MFCD00061126
- EINECS号:672-589-8
- 分子式:C7H2Cl4O2
- 分子量:259.9
- 产品CID: 2291700
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
欧盟法规
ECHA物质C&L通报上下游产品
CAS号117-08-8 四氯苯二甲酸酐 | CAS号69931-41-5 4-(2,3,4,5-tetr... | CAS号6923-69-9 四氯邻氨基苯甲酸 | CAS号632-58-6 四氯酞酸半水合物 | CAS号2136-95-0 1,2,3,4,5-penta... | CAS号27767-65-3 4,5,6,7,7-Penta... | CAS号36245-95-1 2,3,4,5-四氯苯甲腈 | CAS号7732-18-5 水 | CAS号83738-92-5 o-(p-methylbenz... | CAS号68-12-2 N,N-二甲基甲酰胺 | CAS号42221-52-3 2,3,4,5-四氯苯甲酰氯 | CAS号6923-69-9 四氯邻氨基苯甲酸合成工艺路线路线简述
- 6923-69-9 = 50-74-8 + 938-86-3
反应条件:1.1 Reagents: Tetrafluoroboric Acid Solvents: Tetrahydrofuran,Water1.2 Reagents: Amyl Nitrite Solvents: Diethyl Ether; 0 °C; 15 Min,0 °C1.3 0.5 H,Rt1.4 Reagents: Hydrogen Ion Solvents: Water; < Ph 7
标题:Aryne Formation From 1-(2'-Carboxyaryl)-3,3-Dimethyl Triazenes
作者:Buxton,P. Christopher; Heaney,Harry
参考文献:Tetrahedron 日期:1995 卷标:51(13) 页码:3929-38
3,4,5,6-四氯-1,2-苯二甲酸半水合物置于溶剂黄146体系中,化学反应生成 2,3,4,5-四氯苯甲酸
参考文献:Tust,Chemische Berichte,1887,Vol. 20,P. 2441
标题:Tust,Chemische Berichte,1887,Vol. 20,P. 2441
海关参考信息
- 2905110000-甲醇
2906210000-苄醇
2912110000-甲醛
2912210000-苯甲醛 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 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:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.