甲基4-(4-联苯基)-2,4-二氧代丁酸酯 | 63656-27-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 甲基4-(4-联苯基)-2,4-二氧代丁酸酯
• 英文名称: 4-Biphenyl-4-yl-2,4-dioxo-butyric acid methyl ester
• 英文别名: Methyl 2,4-dioxo-4-(4-phenylphenyl)butanoate
• CAS: 63656-27-9
• 化学式: C₁₇H₁₄O₄
• mdl: MFCD07346275
• 分子量: 282.296
• InChiKey: YDYQRPUOLGQGFI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  21
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.117
• 拓扑面积：
  60.4
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 海关编码：
  2918300090

上下游信息

• 下游产品

  中文名称	英文名称	CAS号	化学式	分子量
  4-(4-联苯基)-2,4-二氧代丁酸	4-((1,1'-biphenyl)-4-yl)-2,4-dioxobutanoic acid	85763-16-2	C16H12O4	268.269

反应信息

• 作为反应物：
  描述：

  甲基4-(4-联苯基)-2,4-二氧代丁酸酯 在 sodium hydroxide 作用下， 以 1,4-二氧六环 、 乙醇 为溶剂， 生成 4-(4-联苯基)-2,4-二氧代丁酸
  参考文献：
  名称：

  Inhibitors of glycolic acid oxidase. 4-Substituted-2,4-dioxobutanoic acid derivatives

  摘要：

  Fourteen new 4-substituted 2,4-dioxobutanoic acids have been synthesized. These compounds, all of which contain lipophilic 4-substituents, are potent inhibitors in vitro of porcine liver glycolic acid oxidase. The I50 value of the two most potent representatives, 4-(4'-bromo[1,1'-biphenyl]-4-yl)-2, 4-dioxobutanoic acid (8) and 4-[4'-[[(3,4-dihydro-3-hydroxy-2H-1, 5-benzodioxepin-3-yl)methyl]thio][1,1'-biphenyl]-4-yl]-2, 4-dioxobutanoic acid (13) is 6 X 10(-8)M.

  DOI：

  10.1021/jm00362a020
• 作为产物：
  描述：

  草酸二甲酯 、 联苯单乙酮 在 sodium methylate 作用下， 以 苯 为溶剂， 生成 甲基4-(4-联苯基)-2,4-二氧代丁酸酯
  参考文献：
  名称：

  Inhibitors of glycolic acid oxidase. 4-Substituted-2,4-dioxobutanoic acid derivatives

  摘要：

  Fourteen new 4-substituted 2,4-dioxobutanoic acids have been synthesized. These compounds, all of which contain lipophilic 4-substituents, are potent inhibitors in vitro of porcine liver glycolic acid oxidase. The I50 value of the two most potent representatives, 4-(4'-bromo[1,1'-biphenyl]-4-yl)-2, 4-dioxobutanoic acid (8) and 4-[4'-[[(3,4-dihydro-3-hydroxy-2H-1, 5-benzodioxepin-3-yl)methyl]thio][1,1'-biphenyl]-4-yl]-2, 4-dioxobutanoic acid (13) is 6 X 10(-8)M.

  DOI：

  10.1021/jm00362a020

文献信息

• Organocatalytic Modified Guareschi–Thorpe Type Regioselective Synthesis: A Unified Direct Access to 5,6,7,8-Tetrahydroquinolines and Other Alicyclic[<i>b</i>]-Fused Pyridines
  作者：Pradeep K. Jaiswal、Vashundhra Sharma、Manas Mathur、Sandeep Chaudhary

  DOI：10.1021/acs.orglett.8b02132

  日期：2018.10.5

  An unprecedented organocatalytic, regioselective, modified Guareschi–Thorpe type protocol toward the modular synthesis of 5,6,7,8-tetrahydroquinolines 22a–g and other alicyclic[b]-fused pyridines 23–28 via the identification of Chitosan as a heterogeneous catalyst is reported. This novel strategy is operationally simple and showed a wide range of functional group tolerance and substrate compatibility

  前所未有的有机催化，区域选择性，改良的Guareschi-Thorpe型方案，通过鉴定壳聚糖作为多相催化剂，可模块化合成5,6,7,8-四氢喹啉22a – g和其他脂环式[ b ]稠合吡啶23 – 28。被报道。这种新颖的策略操作简单，并且具有广泛的官能团耐受性和底物相容性。拟议的机制途径涉及亚胺-烯胺级联方法，用于合成结构多样的脂环式[ b ]稠合吡啶杂环。新型抗真菌分子的克级合成和鉴定29 –图31强调了这种方法的实用性。
• ANDREJCHIKOV YU. S.; TOKMAKOVA T. N.; PIDEHMSKIJ E. L.; BOPOHOBA L. A.; V+, XIM. FARMATSEVT. ZH., 1977, 11 HO 5, 85-87
  作者：ANDREJCHIKOV YU. S.、 TOKMAKOVA T. N.、 PIDEHMSKIJ E. L.、 BOPOHOBA L. A.、 V+

  DOI：——

  日期：——
• ANDREJCHIKOV YU. S.; PITIRIMOVA S. G.; CAPAEBA R. F.; GEJN V. L.; PLAXINA+, XIMIYA GETEROTSIKL. SOEDIN., 1978, HO 3 407-410
  作者：ANDREJCHIKOV YU. S.、 PITIRIMOVA S. G.、 CAPAEBA R. F.、 GEJN V. L.、 PLAXINA+

  DOI：——

  日期：——
• Inhibitors of glycolic acid oxidase. 4-Substituted-2,4-dioxobutanoic acid derivatives
  作者：H. W. R. Williams、E. Eichler、W. C. Randall、C. S. Rooney、E. J. Cragoe、K. B. Streeter、H. Schwam、S. R. Michelson、A. A. Patchett、D. Taub

  DOI：10.1021/jm00362a020

  日期：1983.8

  Fourteen new 4-substituted 2,4-dioxobutanoic acids have been synthesized. These compounds, all of which contain lipophilic 4-substituents, are potent inhibitors in vitro of porcine liver glycolic acid oxidase. The I50 value of the two most potent representatives, 4-(4'-bromo[1,1'-biphenyl]-4-yl)-2, 4-dioxobutanoic acid (8) and 4-[4'-[[(3,4-dihydro-3-hydroxy-2H-1, 5-benzodioxepin-3-yl)methyl]thio][1,1'-biphenyl]-4-yl]-2, 4-dioxobutanoic acid (13) is 6 X 10(-8)M.