2,4-二氯-6-(苯基甲基)-苯丙醛 | 99725-28-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2,4-二氯-6-(苯基甲基)-苯丙醛
• 英文名称: 3-(6-benzyl-2,4-dichlorophenyl)propanal
• 英文别名: 2,4-Dichloro-6-(phenylmethyl)-benzenepropanal；3-(2-benzyl-4,6-dichlorophenyl)propanal
• CAS: 99725-28-7
• 化学式: C₁₆H₁₄Cl₂O
• 分子量: 293.193
• InChiKey: VSTWJULEQCHNPW-UHFFFAOYSA-N

物化性质

• 沸点：
  388.2±37.0 °C(Predicted)
• 密度：
  1.224±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  methyl 3-<2,4-dichloro-6-(dimethoxymethyl)phenyl>propionate 在 吡啶 、 氢氧化钾 、 N-氯代丁二酰亚胺 、 lithium aluminium tetrahydride 、 硫酸 、 二甲基亚砜 、 三氟乙酸酐 、 copper(II) oxide 、 copper(ll) bromide 、 肼 作用下， 以 甲醇 、 乙醚 、 二氯甲烷 、 水 、 丙酮 、 二乙二醇 为溶剂， 反应 40.67h， 生成 2,4-二氯-6-(苯基甲基)-苯丙醛
  参考文献：
  名称：

  3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted-[1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives

  摘要：

  The syntheses of a series of 7-(3,5-disubstituted [1,1'-bephenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactones are reported. Intrinsic 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitory activity is enhanced markedly when the biphenyl moiety is substituted by chloro or methyl groups at positions 3 and 5 and a fluoro group at position 4'. These substitutions, followed by resolution, provided compounds 100(+) and 110(+) with 2.8 times the intrinsic inhibitory activity of compactin. Compound 100(+) was shown to possess the same chirality in the lactone ring as compactin by single-crystal X-ray crystallography.

  DOI：

  10.1021/jm00152a002

文献信息

• STOKKER, G. E.;ALBERTS, A. W.;ANDERSON, P. S.;CRAGOE, E. J. ,, JR.;DEANA,+, J. MED. CHEM., 1986, 29, N 2, 170-181
  作者：STOKKER, G. E.、ALBERTS, A. W.、ANDERSON, P. S.、CRAGOE, E. J. ,, JR.、DEANA,+

  DOI：——

  日期：——
• 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted-[1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives
  作者：G. E. Stokker、A. W. Alberts、P. S. Anderson、E. J. Cragoe、A. A. Deana、J. L. Gilfillan、J. Hirshfield、W. J. Holtz、W. F. Hoffman

  DOI：10.1021/jm00152a002

  日期：1986.2

  The syntheses of a series of 7-(3,5-disubstituted [1,1'-bephenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactones are reported. Intrinsic 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitory activity is enhanced markedly when the biphenyl moiety is substituted by chloro or methyl groups at positions 3 and 5 and a fluoro group at position 4'. These substitutions, followed by resolution, provided compounds 100(+) and 110(+) with 2.8 times the intrinsic inhibitory activity of compactin. Compound 100(+) was shown to possess the same chirality in the lactone ring as compactin by single-crystal X-ray crystallography.