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(1-methyl-3-piperidinyl) methyl methyl ether | 131297-57-9

中文名称
——
中文别名
——
英文名称
(1-methyl-3-piperidinyl) methyl methyl ether
英文别名
3-(Methoxymethyl)-1-methylpiperidine
(1-methyl-3-piperidinyl) methyl methyl ether化学式
CAS
131297-57-9
化学式
C8H17NO
mdl
——
分子量
143.229
InChiKey
QCPIRWAFDXWUNY-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):
    0.9
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    12.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为产物:
    参考文献:
    名称:
    Photophysics of saturated amino alcohols: lupinine and model compounds; excited-state intramolecular association
    摘要:
    The absorption and fluorescence properties of the amino alcohol (-)-lupinine (I) are examined in dilute n-hexane solution. They are compared with model compounds quinolizidine (1-azabicyclo[4.4.0]decane, II) and 1-methyl-3-piperidinylmethanol (III). On the basis of the blue shift of the electronic absorption spectra of the hydrogen-bonded forms of I and III, formation constants are determined spectrometrically; these values compare favorably with those determined from IR studies. The fluorescence spectra of I and III are red shifted and broader than those of II and 1-methylpiperidine, respectively; moreover, fluorescence decay of the amino alcohols is biexponential. These properties are associated with the excited-state complex between the amino and hydroxy moieties; this complex is assigned a different structure relative to the ground-state hydrogen-bonded species. The temperature dependence of the fluorescence decay parameters of I is used to estimate the binding energy of the electronically excited intramolecular complex, 13 kJ/mol; this compares with 7.5 kJ/mol, which is the reported stability of the ground-state complex. Comparisons are made with intermolecular amine-water and -ethanol complexes.
    DOI:
    10.1021/j100389a008
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文献信息

  • [EN] SPIRO-FUSED TRICYCLIC MAP4K1 INHIBITORS<br/>[FR] INHIBITEURS DE MAP4K1 TRICYCLIQUES SPIRO FUSIONNÉS
    申请人:BAYER AG
    公开号:WO2021074279A1
    公开(公告)日:2021-04-22
    The present invention relates to Map4K1 inhibitors of formula (I) to pharmaceutical compositions and combinations comprising the compounds according to the invention, and to the prophylactic and therapeutic use of the inventive compounds, respectively to the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular for neoplastic disorders, repectively cancer or conditions with dysregulated immune responses or other disorders associated with aberrant MAP4K1 signaling, as a sole agent or in combination with other active ingredients. The present invention further relates to the use, respectively to the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of protein inhibitors in benign hyperplasias, atherosclerotic disorders, sepsis, autoimmune disorders, vascular disorders, viral infections, in neurodegenerative disorders, in inflammatory disorders, in atherosclerotic disorders and in male fertility control.
    本发明涉及式(I)的Map4K1抑制剂,以及包含根据本发明的化合物的药物组合物和组合物,以及创新化合物的预防性和治疗性用途,分别用于制造用于治疗或预防疾病的药物组合物,特别是用于肿瘤性疾病,癌症或与异常MAP4K1信号相关的其他紊乱免疫反应或其他紊乱的疾病,作为单一药剂或与其他活性成分组合使用。本发明还涉及使用,分别用于制造用于治疗或预防良性增生、动脉粥样硬化疾病、败血症、自身免疫疾病、血管疾病、病毒感染、神经退行性疾病、炎症性疾病、动脉粥样硬化疾病和男性生育控制的蛋白抑制剂的药物组合物的用途。
  • Photochromic Indeno-Fused Ring Pyran Compounds
    申请人:Transitions Optical, Inc.
    公开号:US20150141661A1
    公开(公告)日:2015-05-21
    The present invention relates to photochromic indeno-fused ring pyran compounds represented by the following Formula (I-A): The present invention also relates to photochromic dichroic compounds, such as represented by Formula (I-A), in which (i) Z 2 is a group N—R 13 in which R 13 is a group L, and (ii) optionally at least one R 1 independently for each n is selected from a group L, in which the group L independently in each case is a lengthening group that provides the photochromic compound with dichroic properties, in accordance with some embodiments. The present invention also relates to photochromic articles, such as photochromic ophthalmic articles, that include one or more photochromic compounds according to the present invention, such as represented by Formula (I-A).
    本发明涉及由以下式(I-A)表示的光致变色吲哚融合环吡喃化合物。本发明还涉及光致二向色化合物,例如由式(I-A)表示,其中(i)Z2是一个N—R13基团,其中R13是一个L基团,以及(ii)对于每个n,可选地至少选择一个R1,每种情况下独立选择自L基团,其中每种情况下L基团是一个提供光致化合物二向色性能的延伸基团,符合某些实施例。本发明还涉及光致物品,例如光致眼科物品,包括根据本发明的一个或多个光致化合物,例如由式(I-A)表示。
  • NOVEL SUBSTITUTED TRIAZOLE DERIVATIVES AS GAMMA SECRETASE MODULATORS
    申请人:Van Brandt Sven Franciscus Anna
    公开号:US20120295891A1
    公开(公告)日:2012-11-22
    The present invention is concerned with novel substituted triazole derivatives of Formula (I) wherein Het 1 , R 1 , R 2 , A 1 , A 2 , A 3 , A 4 , L 1 , and L 2 have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.
    本发明涉及具有以下式(I)的新型取代三唑衍生物,其中Het1,R1,R2,A1,A2,A3,A4,L1和L2的含义如权利要求中所定义。根据本发明的化合物可用作γ-分泌酶调节剂。本发明还涉及制备这种新型化合物的方法,包括将所述化合物作为活性成分的药物组合物以及将所述化合物用作药物的用途。
  • PHOTOCHROMIC MATERIALS THAT INCLUDE 6-AMINO SUBSTITUTED INDENO-FUSED NAPHTHOPYRANS
    申请人:Chopra Anu
    公开号:US20120053341A1
    公开(公告)日:2012-03-01
    The present invention relates to photochromic materials that include certain indeno-fused naphthopyrans. The indeno-fused naphthopyrans have an amino group (e.g., a piperidino or morpholino group) bonded to the 6-position and an optional halo group (e.g., fluoro) bonded to the 11-position thereof. The photochromic materials of the present invention may have a closed-form electromagnetic radiation absorption spectrum that is shifted to longer wavelengths (e.g., wavelengths of greater than 390 nm), relative to comparable photochromic materials. The present invention also relates to optical elements, such as eyeglasses, that include the photochromic materials of the present invention.
    本发明涉及包括某些吲哚并螺[3,3,3]己喹喙的光致变色材料。这些吲哚并螺[3,3,3]己喹喙在6位与氨基团(例如哌啶基或吗啉基)键合,并且在11位可能与卤素基团(例如氟基)键合。本发明的光致变色材料可能具有闭合形式的电磁辐射吸收光谱,其相对于类似的光致变色材料向更长波长(例如大于390纳米的波长)移动。本发明还涉及包括本发明的光致变色材料的光学元件,例如眼镜。
  • METHOD OF MAKING INDENO-FUSED NAPHTHOL MATERIALS
    申请人:Chopra Anu
    公开号:US20120157696A1
    公开(公告)日:2012-06-21
    The present invention relates to a method of making indeno-fused naphthol materials, that involves, with some embodiments, forming an indanone acid intermediate, which can be represented by the following general Formula V, With Formula V, m is from 0 to 4, and R 1 for each m, R g and R h can each be independently selected from, for example, hydrogen and hydrocarbyl. The present invention also relates to a method of making an indeno-fused naphthopyran that involves an indanone acid intermediate synthetic route.
    本发明涉及一种制备茚并萘酚材料的方法,其中在某些实施例中,涉及形成一种茚酮酸中间体,该中间体可以用以下一般式V表示,式中,m取值范围为0至4,对于每个m,Rg和Rh可以分别独立地选择为氢和烃基。本发明还涉及一种制备茚并萘吡喃的方法,该方法涉及一种茚酮酸中间体的合成路线。
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