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1-(4-butoxy-3-methyl-phenyl)-ethanone | 14794-63-9

中文名称
——
中文别名
——
英文名称
1-(4-butoxy-3-methyl-phenyl)-ethanone
英文别名
1-(4-Butoxy-3-methyl-phenyl)-aethanon;1-(4-Butoxy-3-methylphenyl)ethanone;1-(4-butoxy-3-methylphenyl)ethanone
1-(4-butoxy-3-methyl-phenyl)-ethanone化学式
CAS
14794-63-9
化学式
C13H18O2
mdl
——
分子量
206.285
InChiKey
JFPSDQKIDROJSD-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):
    3.2
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    26.3
  • 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

  • 作为反应物:
    描述:
    1-(4-butoxy-3-methyl-phenyl)-ethanone氢氧化钾 作用下, 生成 2-(4-butoxy-3-methyl-phenyl)-quinoline
    参考文献:
    名称:
    de Clercq; Buu-Hoi, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1948, vol. 227, p. 1251
    摘要:
    DOI:
  • 作为产物:
    描述:
    1-n-butoxy-2-methylbenzene乙酸酐 在 [t-BuCpZr(OH2)3]22-OH)2(OSO2C8F17)4*2(C3H6O)*8H2O 作用下, 以 neat (no solvent) 为溶剂, 以85%的产率得到1-(4-butoxy-3-methyl-phenyl)-ethanone
    参考文献:
    名称:
    空气稳定的μ 2 -羟基桥接阳离子锆茂全氟辛基磺酸的双核配合物:它们的结构,表征和应用
    摘要:
    通过用(RCp)2 ZrCl 2 [R = H,n -Bu,t -Bu]处理C 8 F 17 SO 3 Ag成功地合成了三种空气稳定的锆茂全氟辛烷磺酸盐。根据X-射线分析,它们具有μ 2 -羟基桥接阳离子双核结构:(我)[CpZr(OH 2)3 ] 2(μ 2 -OH)2(OSO 2 ç 8 ˚F 17)4 ·2THF·4H 2 O(1a ·2THF·4H2 O),(II)[ Ñ -BuCpZr(OH 2)3 ] 2(μ 2 -OH)2(OSO 2 ç 8 ˚F 17)4 ·6H 2 O(图2a ·6H 2 O),和(III) [吨-BuCpZr(OH 2)3 ] 2(μ 2 -OH)2(OSO 2 ç 8 ˚F 17)4 ·2C 3 ħ 6O·8H 2 O(3a ·2C 3 H 6 O·8H 2 O)。复合物中水和有机分子的配体在重结晶过程中源自潮湿的空气和溶剂。这些配合物用不同的技术表
    DOI:
    10.1016/j.tet.2018.02.057
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文献信息

  • Strong Lewis Acids of Air-Stable Metallocene Bis(perfluorooctanesulfonate)s as High-Efficiency Catalysts for Carbonyl-Group Transformation Reactions
    作者:Renhua Qiu、Xinhua Xu、Lifeng Peng、Yalei Zhao、Ningbo Li、Shuangfeng Yin
    DOI:10.1002/chem.201103874
    日期:2012.5.14
    that 2 a and 2 b were thermally stable at 300 and 180 °C, respectively. These complexes exhibited unusually high solubility in polar organic solvents. Conductivity measurement showed that the complexes (2 a and 2 b) were ionic dissociation in CH3CN solution. X‐ray analysis result confirmed 2 a⋅3 H2O⋅THF was a cationic organometallic Lewis acid. UV/Vis spectra showed a significant red shift due to the
    强路易斯酸空气中稳定的金属茂双(全氟辛烷磺酸盐)S [M(CP)2 ] [OSO 2 C ^ 8 ˚F 17 ] 2 ⋅ Ñ ħ 2 O⋅THF(M = Zr的(2 ⋅3ħ 2 O⋅THF ),M =的Ti(图2b ⋅2ħ 2 O⋅THF))由[M(CP)的反应合成2 ]氯2(M = Zr的(1),M =的Ti(图1b)),与n BuLi和C 8 F 17 SO 3 H(2当量)或与C 8 F 17 SO 3Ag(2当量)。这些配合物的水合物数(n)是可变的,取决于条件从0变为4。与众所周知的茂金属三氟甲磺酸盐相反,这些络合物在露天环境中一年没有变化。热重-差示扫描量热(TG-DSC)分析表明,2和图2b分别为300和180℃,是热稳定的。这些配合物在极性有机溶剂中显示出异常高的溶解度。电导率测量表明,络合物(2a和2b)在CH 3 CN溶液中呈离子离解。X射线分析结果确认为2 a⋅3H
  • Synthesis and structure of an air-stable μ2-hydroxy-bridged binuclear complex of bis(methylcyclopentadienyl)dizirconium(IV) perfluorooctanesulfonate and its application in Lewis acid-catalyzed reactions
    作者:Xiaohong Zhang、Cong Lou、Ningbo Li、Xinhua Xu、Renhua Qiu、Shuangfeng Yin
    DOI:10.1016/j.jorganchem.2013.10.004
    日期:2014.1
    Air-stable binuclear complex of bis(methylcyclopentadienyl)zirconium perfluorooctanesulfonate (1a) was successfully synthesized by the reaction of (CH3Cp)2ZrCl2 with C8F17SO3Ag. The compound 1a was characterized by different techniques and found to have the nature of air-stability, water tolerance, thermally-stability and strong Lewis-acidity. In addition, its solubility was higher than that of our
    通过(CH 3 Cp)2 ZrCl 2与C 8 F 17 SO 3 Ag反应成功地合成了双(甲基环戊二烯基)全氟辛烷磺酸锆(1a)的空气稳定双核络合物。化合物1a用不同的技术表征,发现具有空气稳定性,耐水性,热稳定性和强路易斯酸度的性质。此外,它的溶解度高于我们先前报道的单核锆茂双(全氟辛烷磺酸盐)的溶解度。它在烷基芳基醚的Friedel-Crafts酰化反应和Mannich反应中显示出很高的催化效率,可以重复使用。
  • 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole and estrogen formulations
    申请人:Pickar Harrison James
    公开号:US20070135396A1
    公开(公告)日:2007-06-14
    The present invention relates to new formulations containing one or more estrogens and 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole compounds which are useful as estrogenic agents, as well as pharmaceutical compositions and methods of treatment utilizing these compounds, which have the general structures below:
    本发明涉及一种新的制剂,其中包含一种或多种雌激素和2-苯基-1-[4-(2-氨基乙氧基)苄基]-吲哚化合物,它们可用作雌激素类药物,以及使用这些化合物的制药组合物和治疗方法,其具有以下一般结构:
  • 2-Phenyl-1-[4-(2-aminoethoxy)-benzyl]-indoles as estrogenic agents
    申请人:Miller P. Chris
    公开号:US20080021017A1
    公开(公告)日:2008-01-24
    The present invention relates to new 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole compounds having the general structures below: which are useful in contraception and in treating melanoma, osteoporosis, acne, dysfunctional uterine bleeding, endometrial polyps, benign breast disease, adenomyosis, infertility, endometriosis, endometrial cancer, polycystic ovary syndrome, cardiovascular disease, Alzheimer's disease, cognitive decline, central nervous system disorders, central nervous system cancers, leukemia, endometrial ablations, chronic renal disease, chronic hepatic disease, coagulation diseases and disorders, hypocalcemia, hypercalcemia, Paget's disease, osteomalacia, osteohalisteresis, and multiple myeloma.
    本发明涉及新的2-苯基-1-[4-(2-氨基乙氧基)苄基]-吲哚化合物,其具有以下一般结构: 这些化合物在避孕和治疗黑色素瘤、骨质疏松症、痤疮、功能性子宫出血、子宫内膜息肉、良性乳腺疾病、子宫腺肌病、不孕不育、子宫内膜异位症、子宫内膜癌、多囊卵巢综合症、心血管疾病、阿尔茨海默病、认知能力下降、中枢神经系统疾病、中枢神经系统癌症、白血病、子宫内膜消融、慢性肾脏疾病、慢性肝病、凝血疾病和紊乱、低钙血症、高钙血症、帕吉特病、软骨发育不全症和多发性骨髓瘤方面有用。
  • 2-PHENYL-1-[4-(2-AMINOETHOXY)-BENZYL]-INDOLE AND ESTROGEN FORMULATIONS
    申请人:PICKAR James Harrison
    公开号:US20120252769A1
    公开(公告)日:2012-10-04
    The present invention relates to new formulations containing one or more estrogens and 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole compounds which are useful as estrogenic agents, as well as pharmaceutical compositions and methods of treatment utilizing these compounds, which have the general structures below:
    本发明涉及一种包含一种或多种雌激素和2-苯基-1-[4-(2-氨乙氧基)-苯基]-吲哚化合物的新配方,这些化合物可用作雌激素类药剂,以及利用这些化合物的制药组合物和治疗方法,这些化合物具有以下一般结构:
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