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(E)-7-methyl-2-octenoic acid | 1258519-35-5

中文名称
——
中文别名
——
英文名称
(E)-7-methyl-2-octenoic acid
英文别名
(E)-7-methyloct-2-enoic acid
(E)-7-methyl-2-octenoic acid化学式
CAS
1258519-35-5
化学式
C9H16O2
mdl
——
分子量
156.225
InChiKey
QEIAQASOSOCTKP-FNORWQNLSA-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):
    2.9
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 下游产品
    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)-7-methyl-2-octenoic acid草酰氯N,N-二甲基甲酰胺 作用下, 以 为溶剂, 反应 0.5h, 生成 7-methyl-2-octenoyl chloride
    参考文献:
    名称:
    Synthesis and biological activities of flavolipids
    摘要:
    Syntheses of the bacterial surfactants 6S 6S- 9S 9S- and 9U 9U-flavolipids confirmed the structures proposed for them from spectroscopic analysis of a flavolipid mixture and made pure flavolipids available for the first time All three synthetic flavolipids and a straight chain analogue were found to be weakly cytotoxic and to inhibit metastatic cancer cell migration with 9U 9U-fiavolipid (the most abundant natural flavolipid) having the most activity Biosynthetic routes to the branched side-chains of the flavolipids are suggested and it is proposed that branched chains are employed to hinder biodegradation (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.tet.2010.09.088
  • 作为产物:
    描述:
    5-甲基-1-己醇草酰氯 、 sodium hydride 、 二甲基亚砜 、 lithium hydroxide 作用下, 以 四氢呋喃乙二醇二甲醚二氯甲烷 为溶剂, 反应 7.5h, 生成 (E)-7-methyl-2-octenoic acid
    参考文献:
    名称:
    链霉菌天蓝色解离的脂肪酸合酶的FabG和FabI的表征。
    摘要:
    功能性串扰:鉴定并鉴定了来自天蓝色链霉菌的β-酮酰基-酰基载体蛋白(ACP; FabG)和烯酰-ACP还原酶(FabI)。动力学分析表明,这些酶可处理直链和支链底物,以及来自脂肪酸和十一烷基脯氨酸的生物合成途径中的ACP。这种松弛的底物特异性使这些酶参与了两个过程。
    DOI:
    10.1002/cbic.201402670
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文献信息

  • US6020371A
    申请人:——
    公开号:US6020371A
    公开(公告)日:2000-02-01
  • [EN] HYDROCAPSULES AND METHOD OF PREPARATION<br/>[FR] HYDROCAPSULES ET LEUR PROCEDE DE PREPARATION
    申请人:ANALYTICAL RES SYSTEMS
    公开号:WO2003059503A1
    公开(公告)日:2003-07-24
    A method is described for the formation of microcapsules which contain a liquid composition in the core, which is surrounded by a polymeric shell, membrane, or coating. The microcapsules are produced by simultaneously extruding the liquid core material along with a polymerizable liquid through concentrically-aligned nozzles to form spherically-layered biliqued droplets, followed by energy input in the form of heat or light which causes polymerization of the outer layer. The capsules formed by this method are capable of containing a variety of liquid materials having a composit ion ranging from completely aqueous to completely non-aqueous.
  • Characterization of FabG and FabI of the<i>Streptomyces coelicolor</i>Dissociated Fatty Acid Synthase
    作者:Renu Singh、Kevin A. Reynolds
    DOI:10.1002/cbic.201402670
    日期:2015.3.2
    Functional crosstalk: β‐Ketoacyl‐acyl carrier protein (ACP; FabG) and enoyl‐ACP reductase (FabI) from Streptomyces coelicolor were identified and characterized. Kinetic analysis demonstrated that these enzymes process straight and branched‐chain substrates along with the ACPs from both fatty acid and undecylprodiginine biosynthetic pathways. This relaxed substrate specificity allow these enzymes to
    功能性串扰:鉴定并鉴定了来自天蓝色链霉菌的β-酮酰基-酰基载体蛋白(ACP; FabG)和烯酰-ACP还原酶(FabI)。动力学分析表明,这些酶可处理直链和支链底物,以及来自脂肪酸和十一烷基脯氨酸的生物合成途径中的ACP。这种松弛的底物特异性使这些酶参与了两个过程。
  • Synthesis and biological activities of flavolipids
    作者:Samiul M. Ahad、Alison L. Ange、Robert B. Bates、Bonnie L. Bell、Adria A. Bodour、Bryan R. Bourne、Cristina G. Contreras、Emily L. Goldberg、A.A. Leslie Gunatilaka、Sheryl King、Albert K. Lee、Rebecca L. Low、Raina M. Maier、Kathryn M. Marlor、Marilyn T. Marron、Ryan C. Scolnik、Matthew J. Streeter、Malgorzata Strelczuk、Long N. Trinh、Vu K. Truong、Sage P. Vissering、Megan C. Weick、Maria T. Williams
    DOI:10.1016/j.tet.2010.09.088
    日期:2010.11
    Syntheses of the bacterial surfactants 6S 6S- 9S 9S- and 9U 9U-flavolipids confirmed the structures proposed for them from spectroscopic analysis of a flavolipid mixture and made pure flavolipids available for the first time All three synthetic flavolipids and a straight chain analogue were found to be weakly cytotoxic and to inhibit metastatic cancer cell migration with 9U 9U-fiavolipid (the most abundant natural flavolipid) having the most activity Biosynthetic routes to the branched side-chains of the flavolipids are suggested and it is proposed that branched chains are employed to hinder biodegradation (C) 2010 Elsevier Ltd All rights reserved
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