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(E)-8-phenyloct-2-enoic acid | 370064-80-5

中文名称
——
中文别名
——
英文名称
(E)-8-phenyloct-2-enoic acid
英文别名
——
(E)-8-phenyloct-2-enoic acid化学式
CAS
370064-80-5
化学式
C14H18O2
mdl
——
分子量
218.296
InChiKey
LAXFLNGOTKUVHH-XYOKQWHBSA-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):
    4.1
  • 重原子数:
    16
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    37.3
  • 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

  • 作为反应物:
    描述:
    (E)-8-phenyloct-2-enoic acid正丁基锂草酰氯三氟甲磺酸二丁硼二甲基氯化铝 作用下, 以 四氢呋喃二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 8.83h, 生成 3-(S)-(5-phenylpentyl)-aziridine-2-(R)-carboxylic acid benzyl ester
    参考文献:
    名称:
    Design and synthesis of MMP inhibitors using N -arylsulfonylaziridine hydroxamic acids as constrained scaffolds
    摘要:
    The synthesis of cis- and trans-aziridine hydroxamic acid derivatives as MMP inhibitors is described using enantio- and diastereoselective methods for the formation of trisubstituted aziridines. Their preliminary inhibitory activity is reported and discussed in the context of modeling studies. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00641-x
  • 作为产物:
    描述:
    (E)-8-phenyloct-2-enoic acid methyl ester 在 lithium hydroxide 作用下, 以 四氢呋喃 为溶剂, 反应 48.0h, 以96%的产率得到(E)-8-phenyloct-2-enoic acid
    参考文献:
    名称:
    Design and synthesis of MMP inhibitors using N -arylsulfonylaziridine hydroxamic acids as constrained scaffolds
    摘要:
    The synthesis of cis- and trans-aziridine hydroxamic acid derivatives as MMP inhibitors is described using enantio- and diastereoselective methods for the formation of trisubstituted aziridines. Their preliminary inhibitory activity is reported and discussed in the context of modeling studies. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00641-x
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文献信息

  • MACROCYCLIZATION OF COMPOUNDS FROM SOLID SUPPORT USING THIOESTERASES
    申请人:Sherman David H.
    公开号:US20090111152A1
    公开(公告)日:2009-04-30
    A method of preparing macrocycles using solid support chemistry and thioesterases is disclosed. Also disclosed are novel macrocycles.
    本发明公开了一种使用固相支持化学和硫酯酶制备大环化合物的方法。同时还公开了新型大环化合物。
  • AMIDE COMPOUND AND USE THEREOF FOR PEST CONTROL
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:US20150005348A1
    公开(公告)日:2015-01-01
    An amide compound represented by formula (I) has an excellent pest control effect. (In the formula, Y represents a 3-7 membered saturated heterocyclic ring which contains, as ring-forming components(s), one or more atoms or groups that are selected from the group consisting of an oxygen atom and —S(O) t —, the saturated heterocyclic ring may have one to three atoms or groups selected from group D and t represents 0 or the like; x represents a C 1 -C 8 chain hydrocarbon group having one group that is selected from group A; W represents —CR 8 — or the like; r represents 1 or the like; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 may be the same or different and each represents a hydrogen atom or the like; and n represents 1 or the like.)
    式(I)所代表的酰胺化合物具有出色的杀虫效果。(在该式中,Y代表一个含有3-7个饱和杂环环的结构,该结构中包含一个或多个从氧原子和-S(O)t-组成的原子或基团,饱和杂环环可能有一个到三个从D组成的原子或基团,t代表0或类似物;x代表一个C1-C8链烃基,其中有一个来自A组的基团;W代表-CR8-或类似物;r代表1或类似物;R1、R2、R3、R4、R5、R6、R7和R8可以相同也可以不同,每个代表一个氢原子或类似物;n代表1或类似物。)
  • US8114640B2
    申请人:——
    公开号:US8114640B2
    公开(公告)日:2012-02-14
  • [EN] MACROCYCLIZATION OF COMPOUNDS FROM SOLID SUPPORT USING THIOESTERASES<br/>[FR] MACROCYCLISATION DE COMPOSÉS À PARTIR D'UN SUPPORT SOLIDE À L'AIDE DE THIOESTÉRASES
    申请人:UNIV MICHIGAN OFFICE OF TECHNO
    公开号:WO2009059002A2
    公开(公告)日:2009-05-07
    A method of preparing macrocycles using solid support chemistry and thioesterases is disclosed. Also disclosed are novel macrocycles.
  • Design and synthesis of MMP inhibitors using N -arylsulfonylaziridine hydroxamic acids as constrained scaffolds
    作者:Stephen Hanessian、Nicolas Moitessier、Louis-David Cantin
    DOI:10.1016/s0040-4020(01)00641-x
    日期:2001.8
    The synthesis of cis- and trans-aziridine hydroxamic acid derivatives as MMP inhibitors is described using enantio- and diastereoselective methods for the formation of trisubstituted aziridines. Their preliminary inhibitory activity is reported and discussed in the context of modeling studies. (C) 2001 Elsevier Science Ltd. All rights reserved.
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