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diphenethyl-amine; hydrochloride | 6332-28-1

中文名称
——
中文别名
——
英文名称
diphenethyl-amine; hydrochloride
英文别名
Diphenaethyl-amin; Hydrochlorid;Bis(2-phenylethyl)amine hydrochloride;2-phenyl-N-(2-phenylethyl)ethanamine;hydrochloride
diphenethyl-amine; hydrochloride化学式
CAS
6332-28-1
化学式
C16H19N*ClH
mdl
MFCD01110386
分子量
261.794
InChiKey
GBMYHLWTKLNQKD-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

  • 熔点:
    233 °C

计算性质

  • 辛醇/水分配系数(LogP):
    3.83
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    16.6
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:7fffa130505525f072eee377995a7e8c
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反应信息

  • 作为反应物:
    描述:
    diphenethyl-amine; hydrochloride 在 ammonium hexafluorophosphate 作用下, 以 为溶剂, 生成 diphenethylammonium hexafluorophosphate
    参考文献:
    名称:
    A Study of the Complexation of Bis(m-Phenylene) Crown Ethers and Secondary Ammonium Ions
    摘要:
    Two macrocycles, bis(m-phenylene)-26-crown-8 (1) and bis(m-phenylene)-32-crown-10 (2), were combined with several linear components, dibenzyl- (3 . PF6), di-n-butyl- (4 . PF6), and diphenethyl-(5 . PF6) ammonium hexafluorophosphate salts. The smaller macrocycle 1 was shown not to complex effectively with any of the ammonium salts in solution by H-1 NMR, but 1:1 complexes were shown to exist in the "gas phase" as [1:3], [1:4], and [1:5] by high-resolution fast atom bombardment mass spectrometry (HRFABMS) and electrospray ionization mass spectrometry (ESIMS). The X-ray crystal structure of macrocycle 1 is reported. The larger macrocycle 2 did form 1:2 complexes with the ammonium salts in solution, which were observed as well in the solid and gas phases. X-ray crystal structures of the pseudorotaxanes [2:(3)(2)]. 2PF(6) and [2:(5)(2)]. 2PF(6) were determined and are discussed. The pseudorotaxanes are stabilized by hydrogen bonding between the ammonium hydrogens of the linear salt unit and the oxygens of the crown ether macrocycle. Secondary stabilization also occurs by edge-to-face pi stacking.
    DOI:
    10.1021/jo972162s
  • 作为产物:
    描述:
    N-benzylidenebenzylamine盐酸 、 sodium tetrahydroborate 作用下, 生成 diphenethyl-amine; hydrochloride
    参考文献:
    名称:
    A Study of the Complexation of Bis(m-Phenylene) Crown Ethers and Secondary Ammonium Ions
    摘要:
    Two macrocycles, bis(m-phenylene)-26-crown-8 (1) and bis(m-phenylene)-32-crown-10 (2), were combined with several linear components, dibenzyl- (3 . PF6), di-n-butyl- (4 . PF6), and diphenethyl-(5 . PF6) ammonium hexafluorophosphate salts. The smaller macrocycle 1 was shown not to complex effectively with any of the ammonium salts in solution by H-1 NMR, but 1:1 complexes were shown to exist in the "gas phase" as [1:3], [1:4], and [1:5] by high-resolution fast atom bombardment mass spectrometry (HRFABMS) and electrospray ionization mass spectrometry (ESIMS). The X-ray crystal structure of macrocycle 1 is reported. The larger macrocycle 2 did form 1:2 complexes with the ammonium salts in solution, which were observed as well in the solid and gas phases. X-ray crystal structures of the pseudorotaxanes [2:(3)(2)]. 2PF(6) and [2:(5)(2)]. 2PF(6) were determined and are discussed. The pseudorotaxanes are stabilized by hydrogen bonding between the ammonium hydrogens of the linear salt unit and the oxygens of the crown ether macrocycle. Secondary stabilization also occurs by edge-to-face pi stacking.
    DOI:
    10.1021/jo972162s
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文献信息

  • Osmium-Promoted Transformation of Alkyl Nitriles to Secondary Aliphatic Amines: Scope and Mechanism
    作者:Juan C. Babón、Miguel A. Esteruelas、Ana M. López、Enrique Oñate
    DOI:10.1021/acs.organomet.0c00236
    日期:2020.6.8
    symmetrical and asymmetrical secondary aliphatic amines promoted by the hexahydride complex OsH6(PiPr3)2 (1) is described, and the mechanisms of the reactions involved are established. Complex 1 catalyzes the aforementioned transformations of aryl-, pyridyl-, and alkoxy-functionalized alkyl nitriles with linear or branched chains. The formation of the secondary amines involves primary imines, primary amines
    描述了由六氢化物配合物OsH 6(P i Pr 3)2(1)促进的烷基腈向对称和不对称仲脂肪族仲胺的转化,并建立了涉及的反应机理。配合物1催化具有直链或支链的芳基,吡啶基和烷氧基官能化的烷基腈的上述转化。仲胺的形成涉及伯亚胺,伯胺和仲亚胺作为有机中间体。反应在温和的条件下(甲苯,100°C和4 bar H 2)进行。1的化学计量反应与新戊腈和2-甲氧基乙腈一起使我们能够分离三氢化物氮杂亚乙烯基衍生物OsH 3 ═N═CHR}(P i Pr 3)2(R = t Bu(3),CH 2 OMe(4))。它们的形成涉及将底物的N–C三键插入不饱和四氢化物OsH 4(P i Pr 3)2(A)的Os–H键中,这是通过从六氢化合物中消除H 2产生的前体。这些三氢化物氮杂亚乙烯基物质与H 2的反应是还原腈的N-C三键的关键步骤。在没有H 2的情况下,A对氮杂亚乙烯基配体的攻击会导致其C(sp 2)–C(sp
  • [EN] 7-ARYL-3,9-DIAZABICYCLO(3.3.1)NON-6-ENE DERIVATIVES AND THEIR USE AS RENIN INHIBITORS IN THE TREATMENT OF HYPERTENSION, CARDIOVASCULAR OR RENAL DISEASES<br/>[FR] DERIVES DE 7-ARYL-3,9-DIAZABICYCLO(3.3.1)NON-6-ENE ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE RENINE DANS LE TRAITEMENT DE L'HYPERTENSION, DE MALADIES CARDIOVASCULAIRES OU RENALES
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2003093267A1
    公开(公告)日:2003-11-13
    The invention relates to novel 3,9-diazabicyclo[3.3.1]nonene derivatives of formula (I) and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors or renin.
    该发明涉及新型3,9-二氮杂双环[3.3.1]壬烯衍生物(I)及相关化合物,以及它们作为药物组合物中活性成分的用途。该发明还涉及相关方面,包括制备这些化合物的过程、含有这些化合物中的一个或多个的药物组合物,尤其是它们作为肾素抑制剂的用途。
  • Synthesis and evaluation of oryzalin analogs against Toxoplasma gondii
    作者:Molla M. Endeshaw、Catherine Li、Jessica de Leon、Ni Yao、Kirk Latibeaudiere、Kokku Premalatha、Naomi Morrissette、Karl A. Werbovetz
    DOI:10.1016/j.bmcl.2010.07.003
    日期:2010.9
    The synthesis and evaluation of 20 dinitroanilines and related compounds against the obligate intracellular parasite Toxoplasma gondii is reported. Using in vitro cultures of parasites in human fibroblasts, we determined that most of these compounds selectively disrupted Toxoplasma microtubules, and several displayed sub-micromolar potency against the parasite. The most potent compound was N(1),N(1)-dipropyl-2,6-dinitro-4-(trifluoromethyl)-1,3-benzenediamine (18b), which displayed an IC(50) value of 36 nM against intracellular T. gondii. Based on these data and another recent report [Ma, C.; Tran, J.; Gu, F.; Ochoa, R.; Li, C.; Sept, D.; Werbovetz, K.; Morrissette, N. Antimicrob. Agents Chemother. 2010, 54, 1453], an antimitotic structure-activity relationship for dinitroanilines versus Toxoplasma is presented. (C) 2010 Elsevier Ltd. All rights reserved.
  • Fileti; Piccini, Gazzetta Chimica Italiana, 1879, vol. 9, p. 294 Anm.
    作者:Fileti、Piccini
    DOI:——
    日期:——
  • 7-ARYL-3,9-DIAZABICYCLO[3.3.1]NON-6-ENE DERIVATIVES AND THEIR USE AS RENIN INHIBITORS IN THE TREATMENT OF HYPERTENSION, CARDIOVASCULAR OR RENAL DISEASES
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP1501830A1
    公开(公告)日:2005-02-02
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