1-(o-Acetoxyphenyl)propyl acetate | 142784-71-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚酯
• 英文名称: 1-(o-Acetoxyphenyl)propyl acetate
• 英文别名: 1-(2-acetoxyphenyl)propyl acetate；[2-(1-Acetyloxypropyl)phenyl] acetate
• CAS: 142784-71-2
• 化学式: C₁₃H₁₆O₄
• 分子量: 236.268
• InChiKey: DZRMDXUCPXGJPT-UHFFFAOYSA-N

物化性质

• 沸点：
  298.5±15.0 °C(Predicted)
• 密度：
  1.105±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  17
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-(o-Acetoxyphenyl)propyl acetate 在 Candida cylindracea lipase 作用下， 以 正己烷 、 正丁醇 为溶剂， 反应 48.0h， 以60%的产率得到1-(o-Hydroxyphenyl)propyl acetate
  参考文献：
  名称：

  Pedrocchi-Fantoni, Giuseppe; Servi, Stefano, Journal of the Chemical Society. Perkin transactions I, 1992, # 8, p. 1029 - 1034

  摘要：

  DOI：
• 作为产物：
  描述：

  2-((tert-butyldimethylsilyl)oxy)benzaldehyde 在 palladium on activated charcoal 吡啶 、 四丁基氟化铵 、 氢气 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 生成 1-(o-Acetoxyphenyl)propyl acetate
  参考文献：
  名称：

  Structure–activity relationships of 1′S-1′-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages

  摘要：

  1'S-1'-Acetoxychavicol acetate from the rhizomes of Alpinia galanga inhibited nitric oxide (NO) production in lipopolysaccharide-activated mouse peritoneal macrophages with an IC50 value of 2.3 mu M. To clarify the structure-activity relationship of 1'S-1'-acetoxychavicol acetate, various natural and synthetic phenylpropanoids and synthetic phenylbutanoids were examined, and the following structural requirements were clarified. (1) The para or ortho substitution of the acetoxyl and 1-acetoxypropenyl groups at the benzene ring was essential. (2) The S configuration of the 1'-acetoxyl group was preferable. (3) The presence of the 3-methoxyl group and disappearance of the 2'-3' double bond by hydrogenation reduced the activity. (4) The substitution of acetyl groups with propionyl or methyl groups reduced the activity. (5) Lengthening of the carbon chain between the 1'- and 2'-positions reduced the activity. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.01.070

文献信息

• 4-hydroxy-benzopyran-2-ones and 4-hydroxy-cycloalkyl\x9bb!pyran-2-ones
  申请人：Pharmacia & Upjohn Company

  公开号：US05686486A1

  公开（公告）日：1997-11-11

  The present invention relates to compounds of formula I which are 4-hydroxy-benzopyran-2-ones and 4-hydroxy-cycloalkyl\x9bb!pyran-2-ones useful for inhibiting a retrovirus in a mammalian cell infected with said retrovirus. ##STR1## Wherein R.sub.10 and R.sub.20 taken together are: ##STR2##

  本发明涉及式I化合物，它们是4-羟基苯并吡喃-2-酮和4-羟基环烷基并吡喃-2-酮，用于抑制哺乳动物细胞中感染的逆转录病毒。其中，R10和R20共同为：##STR2##。
• 4-HYDROXY-BENZOPYRAN-2-ONES AND 4-HYDROXY-CYCLOALKYL B]PYRAN-2-ONES USEFUL TO TREAT RETROVIRAL INFECTIONS
  申请人：THE UPJOHN COMPANY

  公开号：EP0682663A1

  公开（公告）日：1995-11-22
• US5686486A
  申请人：——

  公开号：US5686486A

  公开（公告）日：1997-11-11
• [EN] 4-HYDROXY-BENZOPYRAN-2-ONES AND 4-HYDROXY-CYCLOALKYL[B]PYRAN-2-ONES USEFUL TO TREAT RETROVIRAL INFECTIONS<br/>[FR] 4-HYDROXY-BENZOPYRANE-2-ONES ET 4-HYDROXY-CYCLOALKYLE-[B]PYRANE-2-ONES UTILES POUR LE TRAITEMENT DES INFECTIONS RETROVIRALES
  申请人：THE UPJOHN COMPANY

  公开号：WO1994018188A1

  公开（公告）日：1994-08-18

  (EN) The present invention relates to compounds of formula (I) which are 4-hydroxy-benzopyran-2-ones and 4-hydroxy-cycloalkyl[b]pyran-2-ones useful for inhibiting a retrovirus in a mammalian cell infected with said retrovirus. In formula (I) R10 and R20 taken together are formula (II) or formula (III).(FR) Composés de la formule (I) correspondant à des 4-hydroxy-benzopyrane-2-ones et à des 4-hydroxy-cycloalkyle[b]pyrane-2-ones employés pour l'inhibition d'un rétrovirus dans une cellule de mammifère infectée par ledit rétrovirus. Dans la formule (I) R10 et R20 considérés ensemble sont (II) ou (III).
• Pedrocchi-Fantoni, Giuseppe; Servi, Stefano, Journal of the Chemical Society. Perkin transactions I, 1992, # 8, p. 1029 - 1034
  作者：Pedrocchi-Fantoni, Giuseppe、Servi, Stefano

  DOI：——

  日期：——