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4-(4-(trifluoromethyl)phenoxy)cyclohex-1-en-1-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate

中文名称
——
中文别名
——
英文名称
4-(4-(trifluoromethyl)phenoxy)cyclohex-1-en-1-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
英文别名
4-(4-(Trifluoromethyl)phenoxy)cyclohex-1-en-1-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate;[4-[4-(trifluoromethyl)phenoxy]cyclohexen-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
4-(4-(trifluoromethyl)phenoxy)cyclohex-1-en-1-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate化学式
CAS
——
化学式
C17H12F12O4S
mdl
——
分子量
540.327
InChiKey
IDJZQARTCOYQGN-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):
    6.8
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    61
  • 氢给体数:
    0
  • 氢受体数:
    16

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] PYRIMIDINES AS SODIUM CHANNEL BLOCKERS<br/>[FR] PYRIMIDINES UTILISÉES COMME BLOQUEURS DE CANAUX SODIQUES
    申请人:PURDUE PHARMA LP
    公开号:WO2013030665A1
    公开(公告)日:2013-03-07
    The present disclosure provides substituted pyrimidine compounds of Formula (I), and the pharmaceutically acceptable salts, prodrugs, and solvates thereof, wherein A1, X, A2, W1, W2, W3, E, Z, and R4 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present disclosure are especially useful for treating pain.
    本公开提供了式(I)的取代嘧啶化合物,以及其药用可接受的盐、前药和溶剂化合物,其中A1、X、A2、W1、W2、W3、E、Z和R4的定义如规范中所述。本公开还涉及使用式(I)的化合物来治疗对通道阻滞有响应的疾病。本公开的化合物特别适用于治疗疼痛。
  • PYRIMIDINES AS SODIUM CHANNEL BLOCKERS
    申请人:PURDUE PHARMA L.P.
    公开号:US20140303139A1
    公开(公告)日:2014-10-09
    The present disclosure provides substituted pyrimidine compounds of Formula (I), and the pharmaceutically acceptable salts, prodrugs, and solvates thereof, wherein A 1 , X, A 2 , W 1 , W 2 , E, Z, and R 4 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present disclosure are especially useful for treating pain.
    本公开提供式(I)的取代嘧啶化合物,以及其药学上可接受的盐、前药和溶剂化物,其中A1、X、A2、W1、W2、E、Z和R4的定义如规范中所述。本公开还涉及使用式(I)的化合物治疗对通道阻滞响应的疾病。本公开的化合物特别适用于治疗疼痛。
  • Pyrimidines as sodium channel blockers
    申请人:Ni Chiyou
    公开号:US09163008B2
    公开(公告)日:2015-10-20
    The present disclosure provides substituted pyrimidine compounds of Formula (I), and the pharmaceutically acceptable salts, prodrugs, and solvates thereof, wherein A1, X, A2, W1, W2, E, Z, and R4 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present disclosure are especially useful for treating pain.
    本公开提供了式(I)的取代嘧啶化合物,以及其药学上可接受的盐、前药和溶剂化物,其中A1、X、A2、W1、W2、E、Z和R4的定义如规范中所述。本公开还涉及使用式(I)的化合物治疗对通道阻滞有反应的疾病。本公开的化合物特别适用于治疗疼痛。
  • PYRIMIDINE CARBOXAMIDES AS SODIUM CHANNEL BLOCKERS
    申请人:LOCKMAN Jeffrey
    公开号:US20160009659A1
    公开(公告)日:2016-01-14
    The present disclosure provides substituted pyrimidine carboxamides of Formula (I) and the pharmaceutically acceptable salts and solvates thereof, wherein A 1 , X, A 2 , W 1 , W 2 , W 3 , E, Z, and R 4 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present disclosure are especially useful for treating pain.
    本公开提供了式(I)的取代嘧啶羧酰胺及其药学上可接受的盐和溶剂化物,其中A1、X、A2、W1、W2、W3、E、Z和R4如规范所述。本公开还针对使用式(I)的化合物治疗对通道阻滞有反应的疾病。本公开的化合物特别适用于治疗疼痛。
  • Pyrimidine carboxamides as sodium channel blockers
    申请人:Purdue Pharma L.P.
    公开号:US10196364B2
    公开(公告)日:2019-02-05
    The present disclosure provides substituted pyrimidine carboxamides of Formula (I) and the pharmaceutically acceptable salts and solvates thereof wherein A1, X, A2, W1, W2, W3, E, Z, and R4 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present disclosure are especially useful for treating pain.
    本公开提供了式 (I) 的取代嘧啶羧酰胺及其药学上可接受的盐和溶剂,其中 A1、X、A2、W1、W2、W3、E、Z 和 R4 的定义如说明书所述。本公开还涉及使用式(I)化合物治疗对钠离子通道阻断有反应的疾病。本公开的化合物尤其适用于治疗疼痛。
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