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(4,5-dimethylnaphthalen-1-yl)-N-methylmethanamine | 709649-65-0

中文名称
——
中文别名
——
英文名称
(4,5-dimethylnaphthalen-1-yl)-N-methylmethanamine
英文别名
(4,5-dimethylnaphthalen-1-ylmethyl)methylamine;(4,5-dimethyl-naphthalen-1-ylmethyl)methylamine;1-(4,5-dimethylnaphthalen-1-yl)-N-methylmethanamine
(4,5-dimethylnaphthalen-1-yl)-N-methylmethanamine化学式
CAS
709649-65-0
化学式
C14H17N
mdl
——
分子量
199.296
InChiKey
PMASCQSGVXLKEL-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

  • 沸点:
    330.0±11.0 °C(Predicted)
  • 密度:
    1.007±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Chasing the Proton Culprit from Palladium-Catalyzed Allylic Amination
    摘要:
    We have found that the addition of base has a significant effect on palladium-catalyzed allylic amination. The long-standing problem of controlling the branched-to-linear ratio has been solved. In the presence of DBU and inexpensive, readily available ligands, palladium-catalyzed allylation proceeds under kinetic control, leading to high branched selectivity. Given the widespread utility of palladium-catalyzed allylic amination, we expect that these findings will be relevant in many areas ranging from asymmetric catalysis to target-oriented synthesis.
    DOI:
    10.1021/ja076659n
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文献信息

  • [EN] HETEROCYCLIC COMPOUNDS, METHODS OF MAKING THEM AND THEIR USE IN THERAPY<br/>[FR] COMPOSES HETEROCYCLIQUES, PROCEDES DE PRODUCTION DE CEUX-CI ET UTILISATION DE CEUX-CI DANS UN TRAITEMENT
    申请人:AFFINIUM PHARM INC
    公开号:WO2004052890A1
    公开(公告)日:2004-06-24
    In part, the present invention is directed to antibacterial compounds of formula (I) wherein A is a bicyclic heteroaryl ring or a tricyclic ring and R2 is an heterocyclic residue; L is a bond, or L is alkyl, alkenyl or cycloalkyl.
    在某种程度上,本发明涉及公式(I)的抗菌化合物,其中A是一个双环杂芳基环或三环环,R2是一个杂环残基;L是一个键,或者L是烷基,烯基或环烷基。
  • Compositions comprising multiple bioactive agents, and methods of using the same
    申请人:Berman M. Judd
    公开号:US20060142265A1
    公开(公告)日:2006-06-29
    In part, the present invention is directed to compositions comprising a FabI inhibitor and at least one other bioactive agent. In another part, the present invention is directed to antibacterial compositions comprising a compound of formulas I-III and at least one other antibacterial agent.
    本发明的一部分涉及含有FabI抑制剂和至少一种其他生物活性剂的组合物。另一部分,本发明涉及含有I-III式化合物和至少一种其他抗菌剂的抗菌组合物。
  • Heterocyclic compounds, methods of making them and their use in therapy
    申请人:Berman Judd
    公开号:US20060183908A1
    公开(公告)日:2006-08-17
    In part, the present invention is directed to antibacterial compounds of formula (I) wherein A is a bicyclic heteroaryl ring or a tricyclic ring and R 2 is an heterocyclic residue; L is a bond, or L is alkyl, alkenyl or cycloalkyl.
    部分地,本发明涉及公式(I)中的抗菌化合物,其中A是双环杂芳基环或三环环,并且R2是杂环残基; L是键合或L是烷基,烯基或环烷基。
  • Heterocyclic Compounds, Methods of Making Them and Their Use in Therapy
    申请人:Berman Judd
    公开号:US20110124633A1
    公开(公告)日:2011-05-26
    In part, the present invention is directed to antibacterial compounds.
    部分地,本发明涉及抗菌化合物。
  • Compositions Comprising Multiple Bioactive Agents, and Methods of Using the Same
    申请人:BERMAN JUDD M.
    公开号:US20120010127A1
    公开(公告)日:2012-01-12
    In part, the present invention is directed to compositions comprising a FabI inhibitor and at least one other bioactive agent. In another part, the present invention is directed to antibacterial compositions comprising a compound of formulas I-III and at least one other antibacterial agent.
    本发明的一部分涉及包含FabI抑制剂和至少一种其他生物活性剂的组合物。另一部分涉及包含I-III式化合物和至少一种其他抗菌剂的抗菌组合物。
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