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5-氨基-2-哌啶-1-苯胺 | 50891-33-3

中文名称
5-氨基-2-哌啶-1-苯胺
中文别名
——
英文名称
5-Amino-2-piperidin-1-yl-benzamide
英文别名
5-amino-2-piperidin-1-ylbenzamide
5-氨基-2-哌啶-1-苯胺化学式
CAS
50891-33-3
化学式
C12H17N3O
mdl
MFCD03042683
分子量
219.286
InChiKey
LUAYPIWXMDEQHJ-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):
    1.1
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    72.4
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2933399090

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • PROCESS FOR DYEING IN THE PRESENCE OF OXIDATION BASES COMPRISING AT LEAST ONE SULFONIC, SULFONAMIDE, SULFONE, AMID OR ACID GROUP AND A METAL CATALYST, DEVICE AND READY-TO-USE COMPOSITION
    申请人:L'OREAL
    公开号:US20160143826A1
    公开(公告)日:2016-05-26
    The present invention relates to a process for dyeing human keratin fibres, in which use is made of one or more metal catalysts and a composition (A) comprising: (a) at least 10% by weight of one or more fatty substances, (b) one or more oxidation bases of formula (I) or (II), the addition salts thereof, solvates thereof and mixtures thereof: Formula (I), Formula (II) (c) one or more chemical oxidizing agents other than atmospheric oxygen. The invention also relates to a multi-compartment device and to a composition comprising all of the above-mentioned ingredients.
  • US9872822B2
    申请人:——
    公开号:US9872822B2
    公开(公告)日:2018-01-23
  • Synthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors
    作者:Stevan Pecic、Svetlana Pakhomova、Marcia E. Newcomer、Christophe Morisseau、Bruce D. Hammock、Zhengxiang Zhu、Alison Rinderspacher、Shi-Xian Deng
    DOI:10.1016/j.bmcl.2012.11.084
    日期:2013.1
    A series of potent amide non-urea inhibitors of soluble epoxide hydrolase (sEH) is disclosed. The inhibition of soluble epoxide hydrolase leads to elevated levels of epoxyeicosatrienoic acids (EETs), and thus inhibitors of sEH represent one of a novel approach to the development of vasodilatory and anti-inflammatory drugs. Structure-activities studies guided optimization of a lead compound, identified through high-throughput screening, gave rise to sub-nanomolar inhibitors of human sEH with stability in human liver microsomal assay suitable for preclinical development. Published by Elsevier Ltd.
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