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N-(4-isopropylbenzyl) piperidine | 6947-73-5

中文名称
——
中文别名
——
英文名称
N-(4-isopropylbenzyl) piperidine
英文别名
1-(4-isopropylbenzyl)piperidine;1-[(4-Propan-2-ylphenyl)methyl]piperidine
N-(4-isopropylbenzyl) piperidine化学式
CAS
6947-73-5
化学式
C15H23N
mdl
MFCD28047171
分子量
217.354
InChiKey
AXISIFQFQAODOV-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):
    3.7
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:3ebedf978e32dae244207caaee0c5c1a
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反应信息

  • 作为产物:
    描述:
    哌啶聚合甲醛4-溴异丙苯 在 cobalt(II) bromide 、 作用下, 以 乙腈 为溶剂, 反应 1.0h, 以87%的产率得到N-(4-isopropylbenzyl) piperidine
    参考文献:
    名称:
    An Expedient Three-Component Synthesis of Tertiary Benzylamines
    摘要:
    描述了一种类似于曼尼希反应的锌介导的三组分反应,涉及芳香卤化物、胺和派拉甲醛。该过程通过原位生成芳基锌试剂,使得合成多种功能化的三级苄胺变得简便。
    DOI:
    10.1055/s-0029-1217108
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文献信息

  • DIPHENYL DERIVATIVES AND USES THEREOF
    申请人:NOVARTIS AG
    公开号:US20190077773A1
    公开(公告)日:2019-03-14
    The present disclosure provides a compound of formula (I): or a pharmaceutically acceptable salt thereof, and its therapeutic uses for activating a growth factor pathway, promoting wound healing, promoting tissue repair, and treating hearing loss, skeletal muscle loss, organ degeneration, tissue damage, neurodegeneration, and muscular atrophy. The disclosure further provides pharmaceutical compositions and combinations. The present disclosure also relates to the use of such compounds for research or other non-therapeutic purposes.
    本公开提供了一种公式(I)的化合物: 或其药用可接受的盐,以及其用于激活生长因子途径、促进伤口愈合、促进组织修复以及治疗听力损失、骨骼肌损失、器官退化、组织损伤、神经退化和肌肉萎缩的治疗用途。本公开还提供了药物组合物和组合物。本公开还涉及将此类化合物用于研究或其他非治疗目的。
  • Half-sandwich ruthenium-carbene catalysts: Synthesis, characterization, and catalytic application in the N-alkylation of amines with alcohols
    作者:Murat Kaloğlu
    DOI:10.1016/j.ica.2019.119163
    日期:2019.12
    the synthesis and characterization of new half-sandwich ruthenium complexes containing oxygen functionalised N-aryl and N-alkyl benzimidazol-2-ylidene ligands have been reported. All ruthenium complexes were tested as catalysts for a wide range of substrates in the N-alkylation of secondary cyclic amines such as pyrrolidine and piperidine, and 4-methylaniline which was a primary aromatic amine with
    摘要在这项研究中,已经报道了含有氧官能化的N-芳基和N-烷基苯并咪唑-2-亚烷基配体的新型半三明治钌络合物的合成和表征。所有的钌络合物都被用作催化剂,用于仲环胺(例如吡咯烷和哌啶)和4-甲基苯胺(它是通过醇借入醇与醇形成的芳香族伯胺)的N-烷基化反应中用于多种底物的催化剂。在无溶剂条件下,在120℃,16 h的条件下,以1 mol%的催化剂负载量进行催化反应。所有钌配合物均显示出优异的催化活性,并且选择性地获得了N-烷基化产物。
  • SULFONYL-SUBSTITUTED BENZOHETEROCYCLIC DERIVATIVE, PREPARATION METHOD AND MEDICAL USE THEREOF
    申请人:SHANGHAI HAIYAN PHARMACEUTICAL TECHNOLOGY CO., LTD
    公开号:US20190300506A1
    公开(公告)日:2019-10-03
    The present invention relates to a sulfonyl-substituted benzoheterocyclic derivative, a preparation method and medical use thereof. Particularly, disclosed is a compound of formula (I) or a pharmaceutically acceptable salt, stereoisomer, solvate, or prodrug thereof, and a preparation method and application thereof. The definition of each group in the formula can be found in the specification and the claims.
    本发明涉及一种磺酰基取代的苯杂环衍生物,其制备方法和医疗用途。特别地,公开了一种符合式(I)的化合物或其药学上可接受的盐、立体异构体、溶剂合物或前药,以及其制备方法和应用。在公开说明书和权利要求中可以找到该式中每个基团的定义。
  • USE OF SUBSTITUTED 2-AMIDOBENZIMIDAZOLES, 2-AMIDOBENZOXAZOLES AND 2-AMIDOBENZOTHIAZOLES OR SALTS THEREOF AS ACTIVE SUBSTANCES AGAINST ABIOTIC PLANT STRESS
    申请人:BAYER CROPSCIENCE AG
    公开号:US20150216168A1
    公开(公告)日:2015-08-06
    The use of substituted 2-amidobenzimidazoles, 2-amidobenzoxazoles and 2-amidobenzothiazoles of the general formula (I) or salts thereof where the radicals in the general formula (I) correspond to the definitions given in the description, for enhancing stress tolerance in plants to abiotic stress, for strengthening plant growth and/or for increasing plant yield, and to selected processes for preparing the compounds mentioned above.
    使用通式(I)中的取代2-酰胺苯并咪唑、2-酰胺苯并噁唑和2-酰胺苯并噻唑或其盐,其中通式(I)中的基团与描述中给出的定义相对应,用于增强植物对非生物胁迫的耐受性,加强植物生长和/或增加植物产量,并选择性地用于制备上述化合物的过程。
  • USE OF SUBSTITUTED BENZODIAZEPINONES AND BENZAZEPINONES OR THE SALTS THEREOF AS ACTIVE SUBSTANCES AGAINST ABIOTIC PLANT STRESS
    申请人:BAYER CROPSCIENCE AG
    公开号:US20150218110A1
    公开(公告)日:2015-08-06
    The use of substituted benzodiazepinones and benzazepinones of the general formula (I) or salts thereof where the radicals in the general formula (I) correspond to the definitions given in the description, for enhancing stress tolerance in plants to abiotic stress, for strengthening plant growth and/or for increasing plant yield, and to selected processes for preparing the compounds mentioned above.
    使用通式(I)或其盐的取代苯二氮平酮和苯并氮平酮,其中通式(I)中的基团对应于描述中给出的定义,用于增强植物对非生物胁迫的耐受性,加强植物生长和/或增加植物产量,并选择上述化合物的制备过程。
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