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

1-甲基-4-(1-甲基哌啶-4-基)哌啶 | 15591-62-5

中文名称
1-甲基-4-(1-甲基哌啶-4-基)哌啶
中文别名
——
英文名称
1,1'-dimethyl-4,4'-bipiperidine
英文别名
1,1'-Dimethyl-dodecahydro-[4,4']bipyridyl;1-methyl-4-(1-methylpiperidin-4-yl)piperidine
1-甲基-4-(1-甲基哌啶-4-基)哌啶化学式
CAS
15591-62-5
化学式
C12H24N2
mdl
——
分子量
196.336
InChiKey
LRWFEZNFQMNVGD-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:
    57-59 °C
  • 沸点:
    67-77 °C(Press: 0.1 Torr)
  • 密度:
    0.940±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    6.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:94e444f7907eb0ac10139d3dcebeb5dd
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

点击查看最新优质反应信息

文献信息

  • [EN] BICYCLIC HETEROCYCLIC DERIVATIVES AS MNK1 AND MNK2 MODULATORS AND USES THEREOF<br/>[FR] DÉRIVÉS HÉTÉROCYCLIQUES BICYCLIQUES À TITRE DE MODULATEURS DE MNK1 ET MNK2 ET LEURS UTILISATIONS
    申请人:AGENCY SCIENCE TECH & RES
    公开号:WO2013147711A1
    公开(公告)日:2013-10-03
    The present invention relates to certain compounds (e.g., imidazopyrazine, imidazopyridine, imidazopyridazine and imidazpyrimidine compounds) that act as inhibitors of the MAP kinase interacting kinases MNK2a, MNK2b, MNK1a, and MNK1b. The present invention further relates to pharmaceutical compositions comprising these compounds, and to the use of the compounds for the preparation of a medicament for the prophylaxis and treatment of diseases (e.g., proliferative diseases (e.g., cancer), inflammatory diseases, Alzheimer's disease), as well as methods of treating these diseases.
    本发明涉及某些化合物(例如咪唑吡嗪、咪唑吡啶、咪唑吡嗪和咪唑嘧啶化合物),这些化合物作为MAP激酶相互作用激酶MNK2a、MNK2b、MNK1a和MNK1b的抑制剂。本发明还涉及包含这些化合物的药物组合物,以及利用这些化合物制备用于预防和治疗疾病(例如增生性疾病(例如癌症)、炎症性疾病、阿尔茨海默病)的药物的用途,以及治疗这些疾病的方法。
  • BICYCLIC HETEROCYCLIC DERIVATIVES AS MNK1 AND MNK2 MODULATORS AND USES THEREOF
    申请人:Agency for Science, Technology and Research
    公开号:US20140371199A1
    公开(公告)日:2014-12-18
    The present invention relates to certain compounds (e.g., imidazopyrazine, imidazopyridine, imidazopyridazine and imidazpyrimidine compounds) that act as inhibitors of the MAP kinase interacting kinases MNK2a, MNK2b, MNK1a, and MNK1b. The present invention further relates to pharmaceutical compositions comprising these compounds, and to the use of the compounds for the preparation of a medicament for the prophylaxis and treatment of diseases (e.g., proliferative diseases (e.g., cancer), inflammatory diseases, Alzheimer's disease), as well as methods of treating these diseases.
    本发明涉及某些化合物(例如咪唑吡嗪、咪唑吡啶、咪唑吡嗪和咪唑嘧啶化合物),这些化合物作为MAP激酶相互作用激酶MNK2a、MNK2b、MNK1a和MNK1b的抑制剂。本发明还涉及包含这些化合物的药物组合物,以及利用这些化合物制备用于预防和治疗疾病(例如增生性疾病(例如癌症)、炎症性疾病、阿尔茨海默病)的药物的用途,以及治疗这些疾病的方法。
  • Is there a particle-size dependence for the mediation by colloidal redox catalysts of the light-induced hydrogen evolution from water?
    作者:P. Keller、A. Moradpour
    DOI:10.1021/ja00544a004
    日期:1980.11
    Particle-size effects for the catalysis by platinum of the light-induced hydrogen evolution from water, using the (Ru(bpy)/sub 3//sup 2 +//methyl viologen/EDTA) model system, were investigated with widely polydispersed colloidal platinum hydrosols and samples with narrower size distributions obtained from the former hydrosols by centrifugation. The optimum values for the hydrogen-formation rates and
    使用 (Ru(bpy)/sub 3//sup 2 +//methyl viologen/EDTA) 模型系统,用广泛的多分散胶体研究铂催化从水中析氢的粒径效应铂水溶胶和通过离心从以前的水溶胶获得的具有更窄尺寸分布的样品。发现所有研究的催化剂的制氢速率和产率的最佳值非常相似;对于含有多分散或选定的小 (1000 A) 的那些,情况确实如此。事实上,在研究的粒径范围内,没有观察到铂粒径对甲基紫精介导的析氢的影响。这些结果与多相催化领域中催化剂分散效应的研究有关。
  • POSITIVE RESIST COMPOSITION AND PATTERN FORMING METHOD USING THE SAME
    申请人:HIRANO Shuji
    公开号:US20080248419A1
    公开(公告)日:2008-10-09
    A positive resist composition, includes: (A) a resin that has a group having absorption at 248 nm at a main chain terminal of the resin (A), and a pattern forming method uses the composition.
    一种正性光刻胶组合物,包括:(A)一种具有在树脂(A)的主链端具有在248nm处吸收的基团的树脂,并且使用该组合物进行图案形成的方法。
  • BIPIPERIDINYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT
    申请人:Wood Harold B.
    公开号:US20100029688A1
    公开(公告)日:2010-02-04
    Bipiperidinyl compounds of the formula I, are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. Pharmaceutically acceptable salts and solvates are included as well. The compounds are useful as agonists of the g-protein coupled receptor GPR-119.
    公开了式I的双哌啶化合物,可用于治疗或预防2型糖尿病和类似疾病。药学上可接受的盐和溶剂也包括在内。这些化合物是G蛋白偶联受体GPR-119的激动剂。
查看更多