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3-diethylamino-1-[1]naphthyl-propan-1-one; hydrochloride | 5471-14-7

中文名称
——
中文别名
——
英文名称
3-diethylamino-1-[1]naphthyl-propan-1-one; hydrochloride
英文别名
3-Diaethylamino-1-[1]naphthyl-propan-1-on; Hydrochlorid;3-diethylamino-1-(1-naphthyl)-propan-1-one hydrochloride;3-(Diethylamino)-1-naphthalen-1-ylpropan-1-one;hydrochloride
3-diethylamino-1-[1]naphthyl-propan-1-one; hydrochloride化学式
CAS
5471-14-7
化学式
C17H21NO*ClH
mdl
——
分子量
291.821
InChiKey
UEPDEEQTMMXREG-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

物化性质

  • 熔点:
    141-142 °C

计算性质

  • 辛醇/水分配系数(LogP):
    4.18
  • 重原子数:
    20
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    20.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2922399090

SDS

SDS:66feaed4f57604e55b40b39c82604a3f
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反应信息

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文献信息

  • [EN] UROTENSIN II RECEPTOR MODULATORS<br/>[FR] MODULATEURS DU RECEPTEUR DE L'UROTENSINE II
    申请人:ACADIA PHARM INC
    公开号:WO2003104216A1
    公开(公告)日:2003-12-18
    Disclosed are compounds of Formula I, or salts or prodrugs thereof, complexed with a human urotensin II receptor as defined herein. Also disclosed are compounds of Formula II, or salts or prodrugs thereof, as defined herein. Also disclosed are methods of modulating the activity of a urotensin II receptor using a compound of Formula I, or a compound of Formula II, or salts or prodrugs thereof. In addition, methods of treating diseases related to the activity of urotensin II receptors are disclosed.
    本文披露了根据本文所定义的与人类尿嘧啶 II 受体形成络合物的 Formula I 化合物,或其盐或前药。还披露了根据本文所定义的 Formula II 化合物,或其盐或前药。还披露了使用 Formula I 化合物、Formula II 化合物、或其盐或前药来调节尿嘧啶 II 受体活性的方法。此外,还披露了治疗与尿嘧啶 II 受体活性相关疾病的方法。
  • Facile catalyst-free synthesis of 2-vinylquinolines via a direct deamination reaction occurring during Mannich synthesis
    作者:Jichao Xiao、Ye Huang、Zilan Song、Wenhua Feng
    DOI:10.1039/c5ra21304e
    日期:——

    A facile catalyst-free method for the synthesis of 2-vinylquinolines via a direct deamination reaction during Mannich synthesis has been developed.

    一种简便的无催化剂方法已经开发出来,用于在Mannich合成过程中通过直接脱氨化反应合成2-乙烯基喹啉。
  • Urotensin II receptor agents
    申请人:——
    公开号:US20040077529A1
    公开(公告)日:2004-04-22
    Disclosed are compounds of Formula I, or salts or prodrugs thereof, complexed with a human urotensin II receptor 1 as defined herein. Also disclosed are compounds of Formula II, or salts or prodrugs thereof, 2 as defined herein. Also disclosed are methods of modulating the activity of a urotensin II receptor using a compound of Formula I, or a compound of Formula II, or salts or prodrugs thereof. In addition, methods of treating diseases related to the activity of urotensin II receptors are disclosed.
  • CERTAIN KETONIC MANNICH BASES DERIVED FROM 1- AND 2- ACETONAPHTHONE
    作者:S. W. PELLETIER
    DOI:10.1021/jo01136a020
    日期:1952.2
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