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

(9ci)-N,N-二甲基-1H-苯并咪唑-2-甲胺 | 108274-97-1

中文名称
(9ci)-N,N-二甲基-1H-苯并咪唑-2-甲胺
中文别名
1H-苯并咪唑-2-甲胺,N,N-二甲基
英文名称
2-(N,N-Dimethylaminomethyl)-benzimidazol
英文别名
1-(1H-benzimidazol-2-yl)-N,N-dimethylmethanamine;2-(dimethylaminomethyl)-1H-benzimidazole;(1H-benzimidazol-2-ylmethyl)-dimethyl-amine;(Bim)CH2NMe2;1-(1H-Benzo[d]imidazol-2-yl)-N,N-dimethylmethanamine
(9ci)-N,N-二甲基-1H-苯并咪唑-2-甲胺化学式
CAS
108274-97-1
化学式
C10H13N3
mdl
MFCD08436518
分子量
175.233
InChiKey
RKDCAGYQGMMYDS-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:
    350℃
  • 密度:
    1.155
  • 闪点:
    165℃

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    31.9
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090

SDS

SDS:2ca128edb9de1a3104e34e948770a7d9
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:
    参考文献:
    名称:
    Structure–Activity Studies of Divin: An Inhibitor of Bacterial Cell Division
    摘要:
    We describe the synthesis and structure activity relationship (SAR) studies of divin, a small molecule that blocks bacterial division by perturbing the assembly of proteins at the site of cell septation. The bacteriostatic mechanism of action of divin is distinct from other reported inhibitors of bacterial cell division and provides an opportunity for assessing the therapeutic value of a new class of antimicrobial agents. We demonstrate a convenient synthetic route to divin and its analogues, and describe compounds with a 10-fold increase in solubility and a 4-fold improvement in potency. Divin analogues produce a phenotype that is identical to divin, suggesting that their biological activity comes from a similar mechanism of action. Our studies indicate that the 2-hydroxynaphthalenyl hydrazide portion of divin is essential for its activity and that alterations and substitution to the benzimidazole ring can increase its potency. The SAR study provides a critical opportunity to isolate drug resistant mutants and synthesize photoaffinity probes to determine the cellular target and biomolecular mechanism of divin.
    DOI:
    10.1021/ml400234x
  • 作为产物:
    参考文献:
    名称:
    锰(i)配合物催化的酮和亚胺的转移转移氢化†
    摘要:
    据报道,带有双功能配体的Mn(I)配合物的合成和反应性均包含胺N-H和苯并咪唑片段。在各种配体中,含Mn(I)的N -((1 H-苯并咪唑-2-基)甲基)苯胺配体)配合物在2-丙醇中酮的转移加氢(TH)中表现出更高的反应性。实验确定,苯并咪唑和胺NH质子均在增强催化活性中起着至关重要的作用。使用该系统可以有效地减少各种醛类和酮类。值得注意的是,在该催化剂的存在下,实现了几种亚胺的TH以及不饱和酮的化学选择性还原。进行DFT计算以了解合理的反应机理,该机理揭示了转移氢化反应遵循协调的外球机理。
    DOI:
    10.1039/c8dt05001e
点击查看最新优质反应信息

文献信息

  • QUINOLONES USEFUL AS INDUCIBLE NITRIC OXIDE SYNTHASE INHIBITORS
    申请人:Smith Nicholas D.
    公开号:US20080139558A1
    公开(公告)日:2008-06-12
    The present invention relates to novel quinolones of Formula I that inhibit inducible NOS synthase together with methods of synthesizing and using the compounds including methods for inhibiting or modulating nitric oxide synthesis and/or lowering nitric oxide levels in a patient by administering the compounds for the treatment of disease.
    本发明涉及抑制诱导型NOS合酶的新奎诺化合物(化学式I),以及合成和使用这些化合物的方法,包括通过向患者施用这些化合物来治疗疾病的抑制或调节一氧化氮合成和/或降低一氧化氮平的方法。
  • NOVEL PYRROLIDINE DERIVED BETA 3 ADRENERGIC RECEPTOR AGONISTS
    申请人:Edmondson Scott D.
    公开号:US20120225886A1
    公开(公告)日:2012-09-06
    The present invention provides compounds of Formula (I), pharmaceutical compositions thereof, and method of using the same in the treatment or prevention of diseases mediated by the activation of β3-adrenoceptor.
    本发明提供了公式(I)的化合物,其药物组合物,以及使用它们治疗或预防通过激活β3肾上腺素受体介导的疾病的方法。
  • Titanium complexes bearing bidentate benzimidazole-containing ligands and their behavior in ethylene polymerization
    作者:Damien Zaher、Atanas K. Tomov、Vernon C. Gibson、Andrew J.P. White
    DOI:10.1016/j.jorganchem.2008.09.057
    日期:2008.12
    A series of potentially bidentate benzimidazolyl ligands of the type (Bim)CH2D (where Bim = benzimidazolyl and D = NMe2 L1, NEt2 L2, NPr2i L3, OMe L4 and SMe L5) has been reacted with Ti(NMe2) 4 to give five- and six-coordinate Ti(IV) complexes of the type [(Bim)CH2D] Ti(NMe2)(3) and [(Bim)CH2D](2)Ti(NMe2)(2), respectively. The X-ray structures of [(Bim)CH2OMe] Ti(NMe2)(3), [(Bim)CH2NMe2](2)Ti(NMe2)(2) and [(Bim)-CH2OMe)](2) Ti(NMe2)(2) are reported along with an evaluation of their behavior in ethylene polymerization. (C) 2008 Elsevier B. V. All rights reserved.
  • Jerchel et al., Justus Liebigs Annalen der Chemie, 1952, vol. 575, p. 162,167
    作者:Jerchel et al.
    DOI:——
    日期:——
  • Absorption Spectra of Heterocyclic Compounds. III. Some Benzimidazole Derivatives
    作者:Edgar A. Steck、Frederick C. Nachod、Galen W. Ewing、Nancy H. Gorman
    DOI:10.1021/ja01190a054
    日期:1948.10
查看更多