摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(3-Aminopropyl)cyclopentan-1-one | 1354393-28-4

中文名称
——
中文别名
——
英文名称
2-(3-Aminopropyl)cyclopentan-1-one
英文别名
——
2-(3-Aminopropyl)cyclopentan-1-one化学式
CAS
1354393-28-4
化学式
C8H15NO
mdl
MFCD19215594
分子量
141.213
InChiKey
NYPUQGQAHUBBMM-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):
    0.2
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.875
  • 拓扑面积:
    43.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    正癸酸2-(3-Aminopropyl)cyclopentan-1-oneN,N'-羰基二咪唑 作用下, 以 乙酸乙酯 为溶剂, 反应 24.0h, 生成 N-[3-(2-oxocyclopentyl)propyl]decanamide
    参考文献:
    名称:
    [EN] INHIBITING HYDROCARBON HYDRATE AGGLOMERATION
    [FR] INHIBITION DE L'AGGLOMÉRATION D'HYDRATES D'HYDROCARBURES
    摘要:
    一种抑制碳氢化合物流体中天然气水合物形成的方法包括向碳氢化合物流体中添加一种气体水合物抗凝聚剂,该抗凝聚剂是一种可生物降解的抗凝聚剂,来源于天然存在的物质。
    公开号:
    WO2018218281A1
点击查看最新优质反应信息

文献信息

  • Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity
    申请人:Batt G. Douglas
    公开号:US20050192276A1
    公开(公告)日:2005-09-01
    The present application describes modulators of MCP-1 of formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, wherein X, Z, a, b, c, d, bond g, n, s, R 1 , R 2 , R 4 , R 5 , R 10 , R 12 , and R 13 , are as defined above. In addition, methods of treating and preventing inflammatory diseases such as asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis using said modulators are disclosed.
    本申请描述了公式(I)的MCP-1调节剂,或其立体异构体或药学上可接受的盐,其中X、Z、a、b、c、d、键g、n、s、R1、R2、R4、R5、R10、R12和R13如上所定义。此外,还公开了利用这些调节剂治疗和预防哮喘和过敏疾病等炎症性疾病,以及类风湿关节炎和动脉粥样硬化等自身免疫病理的方法。
  • Substituted fused bicyclic amines as modulators of chemokine receptor activity
    申请人:Batt G. Douglas
    公开号:US20050197373A1
    公开(公告)日:2005-09-08
    The present application describes modulators of CCR3 of formula (Ia) and (Ib): or pharmaceutically acceptable salt forms thereof, wherein Z, R 1 , R 2 , R 3 , R 4 , R 5 , R 5 ′, R 6 , a, b, c, d, and u are as defined herein. In addition, methods of treating and preventing inflammatory diseases such as asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis using said modulators are disclosed.
    本申请描述了公式(Ia)和(Ib)的CCR3调节剂,或其药用盐形式,其中Z、R1、R2、R3、R4、R5、R5'、R6、a、b、c、d和u的定义如本文所述。此外,还公开了利用这些调节剂治疗和预防哮喘和过敏疾病等炎症性疾病,以及类风湿关节炎和动脉粥样硬化等自身免疫病理的方法。
  • Synthesis of a 200-member library of squaric acid N-hydroxylamide amides
    作者:Julie Charton、Benoît P. Déprez、Rébecca F. Déprez-Poulain
    DOI:10.1016/j.bmcl.2008.08.025
    日期:2008.9
    We report here the parallel synthesis of 200 compounds based on squaric acid template. These compounds are obtained via a one-step solution-phase procedure starting from three squaric acid N-hydroxylamide esters precursors. The set of diverse reagents qualified (amines, anilines, amino-alcohols and amino-esters) makes this strategy suitable for the search of biologically active compounds. The library was screened on the zinc metalloenzyme ADAMTS-5 and hits with IC50 in the range of 1-50 mu M were identified. (C) 2008 Elsevier Ltd. All rights reserved.
  • Heterocyclic aspartyl protease inhibitors
    申请人:Merck Sharp & Dohme Corp.
    公开号:EP2343069B1
    公开(公告)日:2016-03-02
  • US7230022B2
    申请人:——
    公开号:US7230022B2
    公开(公告)日:2007-06-12
查看更多