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4-(heptyloxy)-N-methylbenzamide

中文名称
——
中文别名
——
英文名称
4-(heptyloxy)-N-methylbenzamide
英文别名
4-heptoxy-N-methylbenzamide
4-(heptyloxy)-N-methylbenzamide化学式
CAS
——
化学式
C15H23NO2
mdl
——
分子量
249.353
InChiKey
AJQDPVXTIQDCKA-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):
    4.2
  • 重原子数:
    18
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 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:
    描述:
    甲醇4-(庚氧基)苯甲酰胺 在 C54H43ClN3P2Ru(1+)*F6P(1-)caesium carbonate 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以87%的产率得到4-(heptyloxy)-N-methylbenzamide
    参考文献:
    名称:
    甲醇催化钌催化合成N-甲基化酰胺
    摘要:
    实现了在钌(II)催化剂存在下使用甲醇有效合成N-甲基化酰胺的方法。值得注意的是,应用该方法,实现了串联C-甲基化和N-甲基化以合成α-甲基N-甲基化酰胺。此外,进行了一些动力学研究和使用合理的中间体进行的对照实验,以了解这一新颖的方案。此外,进行了详细的计算研究以了解这种转变的机理。
    DOI:
    10.1021/acs.orglett.9b01925
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文献信息

  • PHENYLPROPIONIC ACID DERIVATIVE AND USE THEREOF
    申请人:MORITA Kohei
    公开号:US20130131134A1
    公开(公告)日:2013-05-23
    A compound represented by the following general formula (1) or a salt thereof, which has superior inhibitory activity against type 4 PLA 2 , and thus has prostaglandin and/or leucotriene production suppressing action [X represents a halogen atom, an alkyl group which may be substituted, or the like, Y represents hydrogen atom or an alkyl group which may be substituted, and Z represents hydrogen atom or an alkyl group which may be substituted].
    以下为通式(1)所表示的化合物或其盐,具有优异的对4型磷脂酶A2的抑制活性,因此具有前列腺素和/或白三烯的产生抑制作用 [其中,X代表卤素原子,可被取代的烷基或类似物,Y代表氢原子或可被取代的烷基,Z代表氢原子或可被取代的烷基]。
  • GLP-1 receptor modulators
    申请人:Celgene International II SÀRL
    公开号:US10259823B2
    公开(公告)日:2019-04-16
    Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where “” represents either or both the R and S form of the compound): where A, B, C, Y1, Y2, Z, R1, R2, R3, R4, R5, W1, n, p and q are as defined herein.
    本研究提供了调节胰高血糖素样肽 1(GLP-1)受体的化合物及其合成方法,以及治疗和/或预防使用方法。此类化合物可单独作为 GLP-1 受体的调节剂或增效剂,或与 GLP-1(7-36) 和 GLP-1(9-36)等增量肽一起使用,或与艾塞那肽和利拉鲁肽等肽类疗法一起使用,并具有以下一般结构(其中""代表化合物的 R 和 S 形式中的一种或两种): 其中 A、B、C、Y1、Y2、Z、R1、R2、R3、R4、R5、W1、n、p 和 q 如本文所定义。
  • Composition, retardation plate, and liquid-crystal display device
    申请人:Li Yi
    公开号:US20080090027A1
    公开(公告)日:2008-04-17
    A composition comprising at least one liquid-crystal compound and a polymer having at least one group of the following formula (A) as the constitutive unit thereof: wherein Mp represents a trivalent linking group; L represents a single bond, or a bivalent linking group; X represents a substituted or unsubstituted functional group having a cyclic structure.
  • LIQUID CRYSTAL COMPOSITION, RETARDATION PLATE, LIQUID CRYSTAL DISPLAY DEVICE, AND PROCESS FOR PRODUCING RETARDATION PLATE
    申请人:LI Yi
    公开号:US20100078592A1
    公开(公告)日:2010-04-01
    A composition comprising at least one liquid crystal compound, and at least one polymer is disclosed. The polymer comprises a constitutional unit represented by a following formula (A) and a constitutional unit derived from a monomer having a fluoroaliphatic group(s): wherein Mp represents a trivalent group constituting fully or partially a polymer main chain; L represents a single bond or a divalent linking group; and X represents a substituted or non-substituted aromatic condensed ring group.
  • NOVEL GLP-1 RECEPTOR MODULATORS
    申请人:Celgene International II SÀRL
    公开号:US20170313717A1
    公开(公告)日:2017-11-02
    Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where “ ” represents either or both the R and S form of the compound): where A, B, C, Y 1 , Y 2 , Z, R 1 , R 2 , R 3 , R 4 , R 5 , W 1 , n, p and q are as defined herein.
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