CAS: 4546-48-9; Methyl 2-Phenylquinoline-4-Carboxylate
该化合物是一种属于quinoline衍生物类别的有机化合物,它具有一种quinoline环系统,由双环结构组成,由苯环组成,并装配成一条丙烯环;该化合物的特征是存在一个甲基酯功能组,该功能组有助于其再活性和溶性;甲基2-苯-4-quinolinecarboxylate通常表现出中度到高脂性,使有机溶剂溶解于有机溶液,而水中溶解度较低;它可能显示生物活动,包括潜在的抗微生物或抗癌特性,因为quired muty的结构性特征;该化合物可以通过各种有机反应合成合成,通常涉及适当起始材料的凝固.其应用可能扩大到药物,农业化学品,或作为有机合成的构件,突出其在医药化学和材料科学中的重要性.
- 英文名称Methyl 2-Phenylquinoline-4-Carboxylate
- 中文名称2-苯基-4-喹啉羧酸甲酯
- IUPAC名称methyl 2-phenylquinoline-4-carboxylate
- 其它别名2-Phenyl-Quinoline-4-Carboxylic Acid Methyl Ester; Methyl 2-Phenyl-4-Quinolinecarboxylate; 4-Quinolinecarboxylic Acid, 2-Phenyl-, Methyl Ester; Methyl 2-Phenyl-4-Quinolinecarboxylate 95%; Methyl 2-Phenylquinoline-4-Carboxylatemethyl; Methyl 2-Phenylquinoline-4-Carboxylate
- CAS编号4546-48-9
- MFCD编号:MFCD00006749
- EINECS号:628-332-7
- 分子式:C17H13NO2分子量:263.3
- 产品CID: 1458028
- 产品分类医药中间体 → 喹啉类化合物
物理性质
MSDS等安全信息
欧盟法规
ECHA物质C&L通报上下游产品
cinchophen methanol 2-phenylquinoline-4-carbonyl chloride methyl 2-phenylquinoline-4-carboxylate 1-oxide 2-phenyl-quinoline-4-carboxylic acid-(2-benzo[1,3]dioxol-5-yl-ethylamide) 4-hydroxymethyl-2-phenylquinoline 2-phenylquinolin-4-amine合成工艺路线路线简述
📜2-苯基-4-喹啉羧酸置于氯化亚砜体系中,化学反应 2.75H,反应生成 2-苯基-4-喹啉羧酸甲酯
参考文献:Mercury(II) And Gold(Iii) Derivatives Of 2-Phenyl Pyridines And 2-Phenyl-4-(Methylcarboxylato)Quinoline
标题:Mercury(II) And Gold(Iii) Derivatives Of 2-Phenyl Pyridines And 2-Phenyl-4-(Methylcarboxylato)Quinoline
摘要:Ortho-Mercurated Derivatives Of Several Substituted 2-Phenylpyridines And Of 2-Phenyl-4-(Methylcarboxylato)Quinoline Have Been Prepared And Characterised. C,N-Chelated Gold(Iii) Derivatives,[aucl2(C6H4C5H3Rn)] (R = H,3-Me,3,5-Me-2,4-Pr-N,4-Bu-T) Are Prepared More Efficiently By Trans-Metallation Reactions Than By Direct Reaction Of Aucl4-With The Phenylpyridines. The New Gold Complexes Were Characterised Spectroscopically And A Variety Of Substitution Reactions Have Been Effected. As Is Usual With Unsymmetrical Bidentate Ligands,The Softer Donor Atom Is Found Trans To The N-Donor Of The Pyridine Unit. Crystal-Structure Determinations Are Reported For [au(Oac)(Pmpy)(Py)]Clo4,[au(Ppy)(Dpbt)]Bph4,[au(Ppy)(S2Cnme2)]Bph4 And Aucl(Pqcm)(2) [hppy = 2-Phenylpyridine,Hpmpy = 2-Phenyl-3-Methylpyridine,Hpqcm = 2-Phenyl-4-(Methylcarboxylato)Quinoline]. (C) 2000 Elsevier Science S.A. All Rights Reserved.
DOI:10.1016/s0022-328X(99)00645-2
海关参考信息
- 2902200000-苯
2912110000-甲醛
2915110000-甲酸
2933310010-吡啶 - 💡 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:CN-112048734-A
优先权日:2020-09-11
标题:Regioselective electrochemical synthesis method of nitrogen-containing aromatic heterocyclic carboxylic acid
专利号:CN-118439997-A
优先权日:2024-05-31
标题 :Synthesis method and application of aryl ortho-carbon hydrogen bond functionalization
专利号:CN-113979939-A
优先权日:2021-09-12
标题 :Synthesis method and application of 2-arylquinoline-4-carboxylic ester
专利号:CN-112048734-B
优先权日:2020-09-11
标题:Regioselective electrochemical synthesis method of nitrogen-containing aromatic heterocyclic carboxylic ester
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品牌试剂参考报价(招募中)
📌 第三方产品分析报告
合成参考文献
摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 118.
摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 113.
摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 273.
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