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2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate | 1104307-63-2

中文名称
——
中文别名
——
英文名称
2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate
英文别名
[2-(2-Methoxy-2-oxoethyl)phenyl] 2-(3,4-diethoxyphenyl)acetate
2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate化学式
CAS
1104307-63-2
化学式
C21H24O6
mdl
——
分子量
372.418
InChiKey
XITUDZMTPHSTTJ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    27
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-羟基苯乙酸甲酯3,4-二乙氧基苯乙酸4-二甲氨基吡啶N,N'-二环己基碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 以82%的产率得到2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate
    参考文献:
    名称:
    Synthesis, characterization and structure–activity relationship analysis of novel depsides as potential antibacterials
    摘要:
    Twenty-six depsides were synthesized to screen for their antibacterial activity. All of them were reported for the first time. Their chemical structures were clearly determined by H-1 NMR, C-13 NMR, ESI mass spectra and elemental analyses, coupled with one selected single-crystal structure. All the compounds were assayed for antibacterial activities against three Gram-positive bacterial strains (Bacillus subtilis ATCC 6633, Staphylococcus aureus ATCC 6538 and Streptococcus faecalis ATCC 9790) and three Gram-negative bacterial strains (Escherichia coli ATCC 35218, Pseudomonas aeruginosa ATCC 13525 and Enterobacter cloacae ATCC 13047) by MTT method. Compound 2-(2-methoxy-2-oxoethyl)phenyl 3-nitrobenzoate (C10) and 2-(2-ethoxy-2-oxoethyl)phenyl 3-nitrobenzoate (C23) showed powerful antibacterial activities against B. subtilis with MIC of 0.78 mu g/mL while compound 2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate (C8) and 2-(2-ethoxy-2oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate (C21) exhibited significant antibacterial activities against E. coli with MIC of 1.562 mu g/mL, which were superior to the positive controls penicillin G and kanamycin B, respectively. On the basis of the biological results, structure-activity relationships were discussed. (c) 2008 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2008.04.019
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文献信息

  • Synthesis, characterization and structure–activity relationship analysis of novel depsides as potential antibacterials
    作者:Peng-Cheng Lv、Zhu-Ping Xiao、Rui-Qin Fang、Huan-Qiu Li、Hai-Liang Zhu、Chang-Hong Liu
    DOI:10.1016/j.ejmech.2008.04.019
    日期:2009.4
    Twenty-six depsides were synthesized to screen for their antibacterial activity. All of them were reported for the first time. Their chemical structures were clearly determined by H-1 NMR, C-13 NMR, ESI mass spectra and elemental analyses, coupled with one selected single-crystal structure. All the compounds were assayed for antibacterial activities against three Gram-positive bacterial strains (Bacillus subtilis ATCC 6633, Staphylococcus aureus ATCC 6538 and Streptococcus faecalis ATCC 9790) and three Gram-negative bacterial strains (Escherichia coli ATCC 35218, Pseudomonas aeruginosa ATCC 13525 and Enterobacter cloacae ATCC 13047) by MTT method. Compound 2-(2-methoxy-2-oxoethyl)phenyl 3-nitrobenzoate (C10) and 2-(2-ethoxy-2-oxoethyl)phenyl 3-nitrobenzoate (C23) showed powerful antibacterial activities against B. subtilis with MIC of 0.78 mu g/mL while compound 2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate (C8) and 2-(2-ethoxy-2oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate (C21) exhibited significant antibacterial activities against E. coli with MIC of 1.562 mu g/mL, which were superior to the positive controls penicillin G and kanamycin B, respectively. On the basis of the biological results, structure-activity relationships were discussed. (c) 2008 Elsevier Masson SAS. All rights reserved.
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马来酰亚胺-酰胺-PEG8-四氟苯酚酯 马来酰亚胺-四聚乙二醇-五氟苯酯 马来酰亚胺-三聚乙二醇-五氟苯酚酯 靛酚乙酸酯 间氯苯乙酸乙酯 间乙酰苯甲酸 酚醛乙酸酯 邻苯二酚二乙酸酯 邻甲苯基环己甲酸酯 邻甲氧基苯乙酸酯 辛酸苯酯 辛酸对甲苯酚酯 辛酸-(3-氯-苯基酯) 辛酰溴苯腈 苯酰胺,3,4-二(乙酰氧基)-N-[6-氨基-1,2,3,4-四氢-1-(4-甲氧苯基)-3-甲基-2,4-二羰基-5-嘧啶基]- 苯酚-乳酸 苯酚,4-异氰基-,乙酸酯(ester) 苯酚,4-[(四氢-2H-吡喃-2-基)氧代]-,乙酸酯 苯酚,3-(1,1-二甲基乙基)-,乙酸酯 苯甲醇,4-(乙酰氧基)-3,5-二甲氧基- 苯基金刚烷-1-羧酸酯 苯基氰基甲酸酯 苯基庚酸酯 苯基己酸酯 苯基呋喃-2-羧酸酯 苯基吡啶-2-羧酸酯 苯基十一碳-10-烯酸酯 苯基乙醛酸酯 苯基乙酸酯-d5 苯基丙二酸单苯酯 苯基丙-2-炔酸酯 苯基丁-2,3-二烯酸酯 苯基4-乙基环己烷羧酸 苯基3-乙氧基-3-亚氨基丙酸盐 苯基2-(苯磺酰基)乙酸酯 苯基2-(4-甲氧基苯基)乙酸酯 苯基2-(2-甲氧基苯基)乙酸酯 苯基2-(2-甲基苯基)乙酸酯 苯基-乙酸-(2-甲酰基-苯基酯) 苯基(S)-2-苯基丙酸 苯基(2S,6S)-(顺式-6-甲基四氢吡喃-2-基)乙酸酯 苯基(2R,6S)-(反式-6-甲基四氢吡喃-2-基)乙酸酯 苯乙酸苯酯 苯乙酸对甲酚酯 苯乙酸-3-甲基苯酯 苯乙酸-2-甲氧基苯酯 苯乙酸-2-甲氧基-4-(1-丙烯基)-苯基酯 苯乙酸-2-甲氧-4-(2-丙烯基)苯(酚)酯 苯丙酸去甲睾酮 苄氧羰基-beta-丙氨酸对硝基苯酯