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4-(3-phenylpropyl)phenol | 34591-21-4

中文名称
——
中文别名
——
英文名称
4-(3-phenylpropyl)phenol
英文别名
(3-phenylpropyl)phenol;4-Hydroxy-1-(3-phenyl-propyl)-benzol;4-(3-Phenyl-propyl)-phenol;α-Phenyl-γ-(4-oxy-phenyl)-propan;4-(γ-Phenyl-propyl)-phenol;1-<4-Hydroxy-phenyl>-3-phenyl-propan
4-(3-phenylpropyl)phenol化学式
CAS
34591-21-4
化学式
C15H16O
mdl
——
分子量
212.291
InChiKey
YIZXYWSYCYOOPR-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

物化性质

  • 沸点:
    200 °C(Press: 13 Torr)
  • 密度:
    1.072±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:68469cc91b5a1f9a561e91cd346dfbad
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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:
    4-(3-phenylpropyl)phenol正丁基锂 、 sodium hydride 、 二异丙胺 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 8.5h, 生成 2,2-Dimethyl-5-[4-(3-phenylpropyl)phenoxy]pentanoic acid
    参考文献:
    名称:
    2-取代异丁酸衍生物的合成及其降血脂活性。
    摘要:
    已经合成了一系列2-取代的异丁酸衍生物,并将其评估为降血脂药。已发现化合物11和20降低实验性高血脂症大鼠的血浆总胆固醇水平的程度要大于氯贝特(CF),并将血浆高密度脂蛋白胆固醇的水平增加至与吉非贝齐(GF)相同的程度。这些化合物引起的肝脏重量增加小于CF和GF。
    DOI:
    10.1021/jm00401a022
  • 作为产物:
    描述:
    (E)-3-(4-羟基苯基)-1-苯基丙-2-烯-1-酮 在 20% palladium hydroxide-activated charcoal 、 氢气 作用下, 以 乙酸乙酯 为溶剂, 以23%的产率得到4-(3-phenylpropyl)phenol
    参考文献:
    名称:
    含磺酰胺侧链的还原查耳酮的合成及生物活性
    摘要:
    研究了通过与减少的查尔酮缩合增加脂类溶解性基团,对抗菌素磺胺类药物对疟疾和结核病的生物活性的影响。磺酰胺衍生物(8a – 8d)是通过1,3-二芳基丙烷骨架获得的,该骨架是通过还原相关的查耳酮而制备的,然后通过曼尼希(Mannich)和曼尼希(Mannich)交换反应添加磺酰胺部分。ClogP值表明,8a – 8d以及中间还原的查耳酮和N-烷基化还原的查耳酮(5a – 7a)的亲脂性远高于磺酰胺类药物(1a – 1c))。N-烷基化的还原查耳酮衍生物6和7表现出最高的抗疟疾(恶性疟原虫(NF54株))活性。即使有些ClogP值较高,磺酰胺基团的加入也会减弱活性,而1a – 1c则没有活性。还原的查耳酮5a和5对结核分枝杆菌(H37Rv株)表现出有效的生长抑制作用,但磺酰胺衍生物8a和8d对结核分枝杆菌无活性或微不足道的活性(分别为0和14%)。,尽管ClogP值较高。因此,预期的ClogP
    DOI:
    10.1021/acs.jnatprod.7b00570
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文献信息

  • 2-IMIDAZOLINES
    申请人:Galley Guido
    公开号:US20090018180A1
    公开(公告)日:2009-01-15
    The present invention relates to compounds of formula I wherein X—Y, R 1 , and n are as defined herein and to their pharmaceutically active salts. Compounds of formula I have a good affinity to the trace amine associated receptors (TAARs), especially for TAAR1 and are useful for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及式I的化合物,其中X—Y、R1和n如本文所定义,并且涉及它们的药用活性盐。式I的化合物对痕量胺相关受体(TAARs)具有良好的亲和力,特别是对TAAR1,适用于治疗抑郁症、焦虑障碍、双相情感障碍、注意力缺陷多动障碍(ADHD)、与压力有关的障碍、精神分裂症等精神障碍、帕金森病等神经系统疾病、阿尔茨海默病等神经退行性疾病、癫痫、偏头痛、高血压、物质滥用以及代谢性障碍,如进食障碍、糖尿病、糖尿病并发症、肥胖症、血脂异常、能量消耗和吸收障碍、体温稳态障碍、睡眠和昼夜节律障碍,以及心血管疾病。
  • INDUSTRIAL PROCESS FOR PRODUCTION OF HIGH-PURITY DIARYL CARBONATES
    申请人:Asahi Kasei Chemicals Corporation
    公开号:EP1961731A1
    公开(公告)日:2008-08-27
    It is an object of the present invention to provide a specific process that enables a high-purity diaryl carbonate required for producing a high-quality high-performance aromatic polycarbonate to be produced industrially in a large amount (e.g. not less than 1 ton / hr) stably for a prolonged period of time (e.g. not less than 1000 hours, preferably not less than 3000 hours, more preferably not less than 5000 hours) from a cyclic carbonate and an aromatic monohydroxy compound. When producing a high-purity diaryl carbonate from a cyclic carbonate and an aromatic monohydroxy compound, the above object can be attained by carrying out a process of the present invention which comprises the steps of: (I) producing a dialkyl carbonate and a diol using a reactive distillation column having a specified structure; (II) producing a diaryl carbonate using two reactive distillation columns each having a specified structure; and (III) purifying the diaryl carbonate so as to obtain a high-purity diaryl carbonate.
    本发明的目的是提供一种特定工艺,使得可以在工业上大量稳定地生产所需用于生产高质量高性能芳香族聚碳酸酯的高纯度二芳基碳酸酯(例如,每小时不少于1吨),并且可以在较长时间内(例如,不少于1000小时,最好不少于3000小时,更好不少于5000小时)从环状碳酸酯和芳香族单羟基化合物中生产。当从环状碳酸酯和芳香族单羟基化合物生产高纯度二芳基碳酸酯时,可以通过执行本发明的工艺步骤来实现上述目的,该工艺步骤包括:(I)使用具有特定结构的反应精馏塔生产二烷基碳酸酯和二醇;(II)使用具有特定结构的两个反应精馏塔生产二芳基碳酸酯;和(III)纯化二芳基碳酸酯以获得高纯度二芳基碳酸酯。
  • INDUSTRIAL PROCESS FOR PRODUCTION OF AROMATIC CARBONATE
    申请人:Asahi Kasei Chemicals Corporation
    公开号:EP1961732A1
    公开(公告)日:2008-08-27
    It is an object of the present invention to provide a specific process that enables an aromatic carbonate required for producing a high-quality high-performance aromatic polycarbonate to be produced industrially in a large amount (e.g. not less than 1 ton / hr) stably for a prolonged period of time (e.g. not less than 1000 hours, preferably not less than 3000 hours, more preferably not less than 5000 hours) from a cyclic carbonate and an aromatic monohydroxy compound. When producing an aromatic carbonate from a cyclic carbonate and an aromatic monohydroxy compound, the above object can be attained by carrying out a step of: (I) producing a dialkyl carbonate and a diol using a reactive distillation column having a specified structure, and (II) producing the an aromatic carbonate using a first reactive distillation column having a specified structure.
    本发明的目的是提供一种特定的工艺,使得可以从环状碳酸酯和芳香单羟基化合物中稳定地大量(例如不少于1吨/小时)工业化生产所需用于生产高质量高性能芳香聚碳酸酯的芳香碳酸酯,且在较长时间内(例如不少于1000小时,更好地不少于3000小时,更好地不少于5000小时)。当从环状碳酸酯和芳香单羟基化合物生产芳香碳酸时,可以通过进行以下步骤实现上述目的:(I)使用具有特定结构的反应精馏塔生产二烷基碳酸酯和二元醇,以及(II)使用具有特定结构的第一反应精馏塔生产芳香碳酸。
  • Antimicrobial Properties of Natural Phenols and Related Compounds II: Cinnamylated Phenols and Their Hydrogenation Products
    作者:L. Jurd、K.L. Stevens、A.D. King、K. Mihara
    DOI:10.1002/jps.2600601145
    日期:1971.11
    A variety of nuclear alkylated C-cinnamylphenols were synthesized and tested for antimicrobial activity. These compounds are particularly effective against Gram-positive bacteria.
    合成了多种核烷基化的C-肉桂基酚,并测试了其抗菌活性。这些化合物对革兰氏阳性细菌特别有效。
  • [EN] METHOD AND APPARATUS FOR THE PRODUCTION OF DIARYL CARBONATE<br/>[FR] PROCÉDÉ ET APPAREIL DE PRODUCTION DE CARBONATE DE DIARYLE
    申请人:SABIC GLOBAL TECHNOLOGIES BV
    公开号:WO2016151508A1
    公开(公告)日:2016-09-29
    The present application describes a method for producing diaryl carbonate. The method includes a step of reacting dialkyl carbonate, aromatic alcohol and a catalyst precursor in a first distillation column to give rise to diaryl carbonate. The method includes a step for reacting, in the first distillation column, the aromatic alcohol with the catalyst precursor to produce a catalyst. The method also includes a step of recovering from the first distillation column a first top stream that comprises an alkyl alcohol evolved in the first distillation column. The present application also describes a system for the production of diaryl carbonate. The system includes a first distillation column including one or more inlets.
    本申请描述了一种生产二苯基碳酸酯的方法。该方法包括在第一蒸馏塔中反应二烷基碳酸酯、芳香醇和催化剂前体的步骤,以产生二苯基碳酸酯。该方法包括在第一蒸馏塔中将芳香醇与催化剂前体反应以产生催化剂的步骤。该方法还包括从第一蒸馏塔中回收包含在第一蒸馏塔中产生的烷基醇的第一顶部流的步骤。本申请还描述了一种用于生产二苯基碳酸酯的系统。该系统包括一个第一蒸馏塔,其中包括一个或多个进料口。
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