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2-Piperidinopropylchlorid | 56953-71-0

中文名称
——
中文别名
——
英文名称
2-Piperidinopropylchlorid
英文别名
1-(2-chloro-1-methyl-ethyl)-piperidine;1-(β-chloro-isopropyl)-piperidine;1-(β-Chlor-isopropyl)-piperidin;1-(1-Chloropropan-2-yl)piperidine
2-Piperidinopropylchlorid化学式
CAS
56953-71-0
化学式
C8H16ClN
mdl
MFCD12030777
分子量
161.675
InChiKey
NOCHJUCFKGEGQP-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):
    2.1
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    2-Piperidinopropylchlorid乙醚苯基锂二乙胺 作用下, 生成 1-(3-cyano-2-methyl-3,3-diphenyl-propyl)-1-methyl-piperidinium; iodide
    参考文献:
    名称:
    444.搜索新的止痛药。第四部分 mid基基本侧链的变化
    摘要:
    DOI:
    10.1039/jr9500002158
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 氯化亚砜氯仿 作用下, 生成 2-Piperidinopropylchlorid
    参考文献:
    名称:
    Bockmuehl; Ehrhart, Justus Liebigs Annalen der Chemie, 1949, vol. 561, p. 52,76
    摘要:
    DOI:
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文献信息

  • [EN] NOVEL BENZOPYRAN COMPOUNDS, COMPOSITIONS AND USES THEREOF<br/>[FR] NOUVEAUX COMPOSÉS BENZOPYRANES, COMPOSITIONS ET UTILISATIONS DE CEUX-CI
    申请人:OLEMA PHARMACEUTICALS INC
    公开号:WO2013090921A1
    公开(公告)日:2013-06-20
    Benzopyran compounds with strong anti-estrogenic activity and essentially no estrogenic activity are provided, which are OP- 1038, which is 3-(4-hydroxyphenyl)-4-methyl-2-(4-2-[(3R)-3-methylpyrrolidin-l-yl]ethoxy}phenyl)-2H-chromen-7-ol, and OP-1074, which is (2S)-3-(4-hydroxyphenyl)-4-methyl-2-(4-2-[(3R)-3-methylpyrrolidin- 1 -yl]ethoxy}phenyl)-2H-chromen-7-ol. OP-1074 is a pure anti-estrogen when tested in the agonist mode and a complete anti-estrogen when tested in the antagonist mode. These compounds are useful for the treatment or prevention of a variety of conditions that are modulated through the estrogen receptor in mammals including humans.
    提供具有强抗雌激素活性和基本无雌激素活性的苯并吡喃化合物,其中包括OP-1038,即3-(4-羟基苯基)-4-甲基-2-(4-2-[(3R)-3-甲基吡咯烷-1-基]乙氧基}苯基)-2H-香豆素-7-醇,以及OP-1074,即(2S)-3-(4-羟基苯基)-4-甲基-2-(4-2-[(3R)-3-甲基吡咯烷-1-基]乙氧基}苯基)-2H-香豆素-7-醇。在激动剂模式下测试时,OP-1074是纯抗雌激素,在拮抗剂模式下测试时是完全的抗雌激素。这些化合物对于治疗或预防在哺乳动物,包括人类中通过雌激素受体调节的多种疾病是有用的。
  • Prevention and treatment of cardiac conditions
    申请人:CROSS Maurice R.
    公开号:US20080275036A1
    公开(公告)日:2008-11-06
    The present invention provides a method of treating conditions associated with iron and calcium overload comprising administering an effective amount of dexrazoxane or a non-dexrazoxane compound of formula (IA), (IB), or (IC) or a pharmaceutically acceptable salt, tautomer, or stereoisomer thereof.
    本发明提供了一种治疗与铁和钙过载相关症状的方法,包括给予有效量的地拉唑喜或公式(IA)、(IB)或(IC)的非地拉唑喜化合物或其药用可接受的盐、互变异构体或立体异构体。
  • Novel Benzopyran Compounds, Compositions and Uses Thereof
    申请人:OLEMA PHARMACEUTICALS, INC.
    公开号:US20130178445A1
    公开(公告)日:2013-07-11
    Benzopyran compounds with strong anti-estrogenic activity and essentially no estrogenic activity are provided, which are OP-1038, which is 3-(4-hydroxyphenyl)-4-methyl-2-(4-2-[(3R)-3-methylpyrrolidin-1-yl]ethoxy}phenyl)-2H-chromen-7-ol, and OP-1074, which is (2S)-3-(4-hydroxyphenyl)-4-methyl-2-(4-2-[(3R)-3-methylpyrrolidin-1-yl]ethoxy}phenyl)-2H-chromen-7-ol. OP-1074 is a pure anti-estrogen when tested in the agonist mode and a complete anti-estrogen when tested in the antagonist mode. These compounds are useful for the treatment or prevention of a variety of conditions that are modulated through the estrogen receptor in mammals including humans.
    本发明提供了具有强烈抗雌激素活性和基本无雌激素活性的苯并吡喃化合物,分别为OP-1038和OP-1074。其中,OP-1038为3-(4-羟基苯基)-4-甲基-2-(4-2-[(3R)-3-甲基吡咯烷-1-基]乙氧基}苯基)-2H-香豆素-7-醇,OP-1074为(2S)-3-(4-羟基苯基)-4-甲基-2-(4-2-[(3R)-3-甲基吡咯烷-1-基]乙氧基}苯基)-2H-香豆素-7-醇。在激动剂模式下测试时,OP-1074是纯抗雌激素,而在拮抗剂模式下测试时则是完全抗雌激素。这些化合物可用于治疗或预防哺乳动物,包括人类中通过雌激素受体调节的各种疾病。
  • NOVEL BENZOPYRAN COMPOUNDS, COMPOSITIONS AND USES THEREOF
    申请人:Olema Pharmaceuticals, Inc.
    公开号:US20150197506A1
    公开(公告)日:2015-07-16
    Benzopyran compounds with strong anti-estrogenic activity and essentially no estrogenic activity are provided, which are OP-1038, which is 3-(4-hydroxyphenyl)-4-methyl-2-(4-2-[(3R)-3-methylpyrrolidin-1-yl]ethoxy}phenyl)-2H-chromen-7-ol, and OP-1074, which is (2S)-3-(4-hydroxyphenyl)-4-methyl-2-(4-2-[(3R)-3-methylpyrrolidin-1-yl]ethoxy}phenyl)-2H-chromen-7-ol. OP-1074 is a pure anti-estrogen when tested in the agonist mode and a complete anti-estrogen when tested in the antagonist mode. These compounds are useful for the treatment or prevention of a variety of conditions that are modulated through the estrogen receptor in mammals including humans.
    提供了具有强烈抗雌激素活性和基本无雌激素活性的苯并吡喃化合物,其中包括OP-1038,即3-(4-羟基苯基)-4-甲基-2-(4-2-[(3R)-3-甲基吡咯烷-1-基]乙氧基}苯基)-2H-香豆素-7-醇,和OP-1074,即(2S)-3-(4-羟基苯基)-4-甲基-2-(4-2-[(3R)-3-甲基吡咯烷-1-基]乙氧基}苯基)-2H-香豆素-7-醇。在激动剂模式下测试时,OP-1074是纯抗雌激素,在拮抗剂模式下测试时是完全抗雌激素。这些化合物对于治疗或预防哺乳动物(包括人类)中通过雌激素受体调节的各种疾病是有用的。
  • Schuler,W.A.; Klebe,H., Justus Liebigs Annalen der Chemie, 1962, vol. 653, p. 172 - 180
    作者:Schuler,W.A.、Klebe,H.
    DOI:——
    日期:——
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