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

1-乙基-3-甲基哌啶 | 2162-86-9

中文名称
1-乙基-3-甲基哌啶
中文别名
——
英文名称
1-ethyl-3-methyl-piperidine
英文别名
(+/-)-1-ethyl-3-methyl-piperidine;(+/-)-1-Aethyl-3-methyl-piperidin;1-Aethyl-3-methyl-piperidin;1-ethyl-3-methylpiperidine
1-乙基-3-甲基哌啶化学式
CAS
2162-86-9
化学式
C8H17N
mdl
——
分子量
127.23
InChiKey
YSPBEFPTFBRJBH-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

  • 保留指数:
    908

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 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

安全信息

  • 海关编码:
    2933399090

SDS

SDS:104f6749202835e9a492cd95fba45de9
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    苄基碘1-乙基-3-甲基哌啶 生成 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    Scholtz, Chemische Berichte, 1908, vol. 41, p. 2007
    摘要:
    DOI:
  • 作为产物:
    描述:
    3-甲基哌啶吡啶 、 lithium aluminium tetrahydride 作用下, 以 乙醚氯仿 为溶剂, 反应 36.0h, 生成 1-乙基-3-甲基哌啶
    参考文献:
    名称:
    Eclipsed Conformation of the Exocyclic N−CH2 Bond in N-Neopentylpiperidines and the Stereodynamic Consequences As Studied by Dynamic NMR Spectroscopy and Molecular Mechanics Calculations
    摘要:
    The dynamic stereochemistry of a range of N-neopentylpiperidines 1 with an eclipsed N-CH2-t-Bu bond is compared with that of the corresponding range of N-ethylpiperidines 2 with a gauche N-CH2Me bond. By using dynamic NMR spectroscopy, the relative importance of ring inversion, exocyclic bond rotation, and nitrogen inversion are elucidated and barriers are reported and discussed. Minor populations of the neopentyl-axial-eclipsed conformation are detected directly and identified with the help of molecular mechanics calculations. The corresponding N-alkylpyrrolidines are also reported.
    DOI:
    10.1021/jo9720344
点击查看最新优质反应信息

文献信息

  • HEPATITIS C VIRUS INHIBITORS AND USES THEREOF IN PREPARATION OF DRUGS
    申请人:CHANGZHOU YINSHENG PHARMACEUTICAL CO., LTD.
    公开号:US20170253614A1
    公开(公告)日:2017-09-07
    A series of hepatitis C virus (HCV) inhibitors and compositions and applications thereof in the preparation of drugs for treating chronic HCV infection. Especially, a series of compounds that are used as NS5A inhibitors, and compositions and uses thereof in the preparations of drugs.
    一系列丙型肝炎病毒(HCV)抑制剂及其组合物,以及在制备用于治疗慢性HCV感染的药物时的应用。特别是一系列用作NS5A抑制剂的化合物,以及在药物制剂中的组合物和用途。
  • Insecticidal Benzenedicarboxamide Derivative
    申请人:Wada Katsuaki
    公开号:US20110184188A1
    公开(公告)日:2011-07-28
    The present invention relates to a novel benzenedicarboxamide derivative and the use thereof as an insecticide having the formula (I) wherein the chemical groups W 1 to W 9 , and R 1 to R 3 are as defined here-in.
    本发明涉及一种新型苯二甲酰胺衍生物及其作为杀虫剂的用途,其化学式为(I),其中化学基团W1至W9,以及R1至R3如本文所定义。
  • [EN] NOVEL THIENOPYRIMIDINE DERIVATIVES, PROCESSES FOR THE PREPARATION THEREOF AND THERAPEUTIC USES THEREOF<br/>[FR] NOUVEAUX DÉRIVÉS DE THIÉNOPYRIMIDINE, LEURS PROCÉDÉS DE PRÉPARATION ET LEURS UTILISATIONS THÉRAPEUTIQUES
    申请人:SANOFI SA
    公开号:WO2013150036A1
    公开(公告)日:2013-10-10
    The present invention relates to compounds of formula (I): wherein R6 is -CONH2 or a -C(Rα)(Rβ)(OH) group; R is a substituted phenyl or heteroaryl group; R7 is an optionally substituted aryl or heteroaryl group. Process for the preparation thereof and therapeutic use thereof.
    本发明涉及式(I)化合物的制备过程及其治疗用途:其中R6是-CONH2或一个-C(Rα)(Rβ)(OH)基团;R是一个取代的苯基或杂芳基团;R7是一个可选地取代的芳基或杂芳基团。
  • NOVEL THIENOPYRIMIDINE DERIVATIVES, PROCESSES FOR THE PREPARATION THEREOF AND THERAPEUTIC USES THEREOF
    申请人:CARRY Jean-Christophe
    公开号:US20130261106A1
    公开(公告)日:2013-10-03
    The present invention relates to compounds of formula (I): wherein R6 is —CONH 2 or a —C(R α )(R β )(OH) group; R is a substituted phenyl or heteroaryl group; R7 is an optionally substituted aryl or heteroaryl group. Process for the preparation thereof and therapeutic use thereof.
    本发明涉及具有公式(I)的化合物: 其中R6是—CONH2或—C(Rα)(Rβ)(OH)基团;R是取代的苯基或杂芳基团;R7是可选地取代的芳基或杂芳基团。 其制备过程及其治疗用途。
  • PYRIDINE AND PYRAZINE DERIVATIVES - 083
    申请人:Barlaam Bernard Christophe
    公开号:US20090118305A1
    公开(公告)日:2009-05-07
    The invention concerns pyridine and pyrazine derivatives of Formula I or a pharmaceutically-acceptable salt thereof, wherein each of W, G 1 , G 2 , G 3 , G 4 , J, Ring A, n and R 3 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.
    本发明涉及式I的吡啶和吡嗪衍生物 或其药用可接受的盐,其中W、G 1 、G 2 、G 3 、G 4 、J、环A、n和R 3 各自具有如前文描述中定义的任何含义;它们的制备过程,包含它们的药物组合物以及它们在制造用于治疗细胞增殖性障碍的药物中的应用。
查看更多