(4-methoxyphenyl)[3-methyl-4-(2,3-epoxypropyloxy)phenyl](naphth-1-yl)methane | 586949-89-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (4-methoxyphenyl)[3-methyl-4-(2,3-epoxypropyloxy)phenyl](naphth-1-yl)methane
• 英文别名: (4-Methoxyphenyl)-(3-methyl-4-(2,3-epoxypropyloxy)phenyl)-1-naphth-1-yl-methane；2-[[4-[(4-methoxyphenyl)-naphthalen-1-ylmethyl]-2-methylphenoxy]methyl]oxirane
• CAS: 586949-89-5
• 化学式: C₂₈H₂₆O₃
• 分子量: 410.513
• InChiKey: JKOVUUHWEQHIHW-UHFFFAOYSA-N

物化性质

• 沸点：
  573.1±50.0 °C(Predicted)
• 密度：
  1.168±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  31
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  31
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (4-methoxyphenyl)[3-methyl-4-(2,3-epoxypropyloxy)phenyl](naphth-1-yl)methane 、 正丁胺 以 乙醇 为溶剂， 以41.6%的产率得到(4-methoxyphenyl)[3-methyl-4-(2-hydroxy-3-n-butylaminopropyloxy)phenyl](naphth-1-yl)methane
  参考文献：
  名称：

  Diaryl naphthyl methanes a novel class of anti-implantation agents

  摘要：

  Diaryl naphthyl methanes and the corresponding 1, 2, 3, 4- and 5, 6, 7, 8-tetrahydro naphthyl methane derivatives have been synthesized as novel estrogen receptor binding ligands. The secondary and tertiary amino alkoxy derivatives of diaryl naphthyl and tetrahydro naphthyl methane interact with the estrogen receptor to elicit promising estrogenic, antiestrogenic and implantation inhibition activities in rats. The most active compounds in this series are 7, 9 and 20, cent percent active in preventing implantation in rats at 2.5 mgkg(-1) dose. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2003.12.015
• 作为产物：
  描述：

  (4-methoxyphenyl)(naphthalen-1-yl)methanone 在 sodium tetrahydroborate 、 三氯化铝 、 四氯化钛 、 potassium carbonate 作用下， 以 甲醇 、 正戊烷 、 苯 为溶剂， 生成 (4-methoxyphenyl)[3-methyl-4-(2,3-epoxypropyloxy)phenyl](naphth-1-yl)methane
  参考文献：
  名称：

  Diaryl naphthyl methanes a novel class of anti-implantation agents

  摘要：

  Diaryl naphthyl methanes and the corresponding 1, 2, 3, 4- and 5, 6, 7, 8-tetrahydro naphthyl methane derivatives have been synthesized as novel estrogen receptor binding ligands. The secondary and tertiary amino alkoxy derivatives of diaryl naphthyl and tetrahydro naphthyl methane interact with the estrogen receptor to elicit promising estrogenic, antiestrogenic and implantation inhibition activities in rats. The most active compounds in this series are 7, 9 and 20, cent percent active in preventing implantation in rats at 2.5 mgkg(-1) dose. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2003.12.015

文献信息

• Process for the preparation of diaryl naphthyl methanes
  申请人：Council of Scientific and Industrial Research

  公开号：US06610705B1

  公开（公告）日：2003-08-26

  The invention relates to novel diaryl naphthyl methane compounds having general formula I as shown herein below, and said compounds useful in the treatment of esterogen related disease or syndrome, Pharmaceutical compositions comprising said novel methane derivatives, process for the preparation of the novel methane derivatives and methods for the treatment of esterogen related diseases or syndrome.

  本发明涉及一种新型二芳基萘甲烷化合物，其通式如下所示，所述化合物可用于治疗雌激素相关疾病或综合征，包括含有该新型甲烷衍生物的制药组合物，制备该新型甲烷衍生物的方法以及治疗雌激素相关疾病或综合征的方法。
• US6610705B1
  申请人：——

  公开号：US6610705B1

  公开（公告）日：2003-08-26
• Diaryl naphthyl methanes a novel class of anti-implantation agents
  作者：Neeta Srivastava、Sangita、S Ray、M.M Singh、Anila Dwivedi、Atul Kumar

  DOI：10.1016/j.bmc.2003.12.015

  日期：2004.3

  Diaryl naphthyl methanes and the corresponding 1, 2, 3, 4- and 5, 6, 7, 8-tetrahydro naphthyl methane derivatives have been synthesized as novel estrogen receptor binding ligands. The secondary and tertiary amino alkoxy derivatives of diaryl naphthyl and tetrahydro naphthyl methane interact with the estrogen receptor to elicit promising estrogenic, antiestrogenic and implantation inhibition activities in rats. The most active compounds in this series are 7, 9 and 20, cent percent active in preventing implantation in rats at 2.5 mgkg(-1) dose. (C) 2004 Elsevier Ltd. All rights reserved.