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(3,4-二氯苯基)-哌啶-4-甲酮盐酸盐 | 64638-17-1

中文名称
(3,4-二氯苯基)-哌啶-4-甲酮盐酸盐
中文别名
——
英文名称
(3,4-dichloro-phenyl)-piperidin-4-yl-methanone; hydrochloride
英文别名
4-(3,4-dichlorobenzoyl)piperidine hydrochloride;(3,4-Dichlorophenyl)(piperidin-4-yl)methanone hydrochloride;(3,4-dichlorophenyl)-piperidin-4-ylmethanone;hydrochloride
(3,4-二氯苯基)-哌啶-4-甲酮盐酸盐化学式
CAS
64638-17-1
化学式
C12H13Cl2NO*ClH
mdl
MFCD08544118
分子量
294.608
InChiKey
UKWAMYCXWLQTBC-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):
    2.84
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.416
  • 拓扑面积:
    29.1
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933399090

反应信息

点击查看最新优质反应信息

文献信息

  • N-substituted alpha-arylazacycloalkylmethanamines and their use as
    申请人:A. H. Robins Company Incorporated
    公开号:US05198449A1
    公开(公告)日:1993-03-30
    Novel compounds of the formula below wherein W is azetidine, pyrrolidine or piperidine, Q is a straight chain hydrocarbon radical of 1-4 carbons and may contain a double bond, and ##STR1## Ar is phenyl, pyridinyl or pyrimidinyl, a process for their preparation, and novel intermediates are disclosed. The novel compounds and the pharmaceutical compositions of this invention are useful in the treatment of hypertension, arrhythmias and angina.
    以下是该公式的新化合物,其中W为氮杂环丙烷、吡咯烷或哌嗪,Q为含有1-4个碳原子的直链烃基,可能含有双键,Ar为苯基、吡啶基或嘧啶基。公开了它们的制备方法和新型中间体。该发明的新化合物和药物组合物在治疗高血压、心律失常和心绞痛方面具有用途。
  • US5198449A
    申请人:——
    公开号:US5198449A
    公开(公告)日:1993-03-30
  • [1-[3-(Phenothiazin-10-yl)propyl]-4-piperidinyl]phenylmethanones, a novel class of long-acting neuroleptic agents
    作者:Robert F. Boswell、William J. Welstead、Robert L. Duncan、David N. Johnson、William H. Funderburk
    DOI:10.1021/jm00199a029
    日期:1978.1
    In previous studies the phenyl-4-piperidinylmethanone moiety was shown to be a neuroleptic pharmacophore. A short series of [1-[3-(phenothiazin-10-yl)propyl]-4-piperidinyl]phenylmethanones was prepared and tested for neuroleptic activity using the blockade of d-amphetamine lethality in aggregated mice and suppression of conditioned avoidance behavior as the end points. Most compounds were shown to be potent neuroleptic agents and two were found to possess a long duration of action.
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