摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-hydroxy-α-ethylbenzylalcohol | 22805-42-1

中文名称
——
中文别名
——
英文名称
4-hydroxy-α-ethylbenzylalcohol
英文别名
(+/-)-1-(4-hydroxyphenyl)propan-1-ol;1-(p-Hydroxyphenyl)propan-1-ol;p-α-hydroxyethylphenol;4-(1-hydroxypropyl)phenol;4-(1'-hydroxypropyl)phenol;α-ethyl-4-hydroxy-benzenemethanol
4-hydroxy-α-ethylbenzylalcohol化学式
CAS
22805-42-1
化学式
C9H12O2
mdl
MFCD08443339
分子量
152.193
InChiKey
WEKMUBUZJDWJIR-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:
    284.0±15.0 °C(Predicted)
  • 密度:
    1.123±0.06 g/cm3(Predicted)
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:8b651be4f5d1337de676df0e1120f272
查看

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
  • 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:
    参考文献:
    名称:
    4-hydroxy-benzopyran-2-ones and 4-hydroxy-cycloalkyl\x9bb!pyran-2-ones
    摘要:
    本发明涉及式I化合物,它们是4-羟基苯并吡喃-2-酮和4-羟基环烷基并吡喃-2-酮,用于抑制哺乳动物细胞中感染的逆转录病毒。其中,R10和R20共同为:##STR2##。
    公开号:
    US05686486A1
  • 作为产物:
    描述:
    (1'R,S)-1'-hydroxychavicol 在 palladium on activated charcoal 氢气 作用下, 以 甲醇 为溶剂, 生成 4-hydroxy-α-ethylbenzylalcohol
    参考文献:
    名称:
    Structure–activity relationships of 1′S-1′-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages
    摘要:
    1'S-1'-Acetoxychavicol acetate from the rhizomes of Alpinia galanga inhibited nitric oxide (NO) production in lipopolysaccharide-activated mouse peritoneal macrophages with an IC50 value of 2.3 mu M. To clarify the structure-activity relationship of 1'S-1'-acetoxychavicol acetate, various natural and synthetic phenylpropanoids and synthetic phenylbutanoids were examined, and the following structural requirements were clarified. (1) The para or ortho substitution of the acetoxyl and 1-acetoxypropenyl groups at the benzene ring was essential. (2) The S configuration of the 1'-acetoxyl group was preferable. (3) The presence of the 3-methoxyl group and disappearance of the 2'-3' double bond by hydrogenation reduced the activity. (4) The substitution of acetyl groups with propionyl or methyl groups reduced the activity. (5) Lengthening of the carbon chain between the 1'- and 2'-positions reduced the activity. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.01.070
点击查看最新优质反应信息

文献信息

  • Oxalic Acid-catalyzed Reaction of Alcohols with NaSCN: The Effects of Additives NaI and I<sub>2</sub>
    作者:Hideyoshi Miyake、Yuichi Nakao、Mitsuru Sasaki
    DOI:10.1246/cl.2006.1262
    日期:2006.11
    Oxalic acid-mediated conversion of alcohols to thiocyante and/or isothiocyanate is described. Aliphatic tertiary alcohols give isothiocyanate by the reaction with NaSCN in the presence of I2, whereas they give thiocyanate without it.
    草酸介导的将醇转化为硫氰酸盐和/或异硫氰酸盐的方法被描述。脂肪族叔醇在I2存在下与NaSCN反应生成异硫氰酸盐,而在无I2的情况下生成硫氰酸盐。
  • A molybdenum based metallomicellar catalyst for controlled and chemoselective oxidation of activated alcohols in aqueous medium
    作者:Prabaharan Thiruvengetam、Rajan Deepan Chakravarthy、Dillip Kumar Chand
    DOI:10.1016/j.jcat.2019.06.013
    日期:2019.8
    A surfactant based oxodiperoxo molybdenum complex, which could activate molecular oxygen, has been employed as a catalyst for controlled oxidation of benzylic alcohols to corresponding carbonyls. The oxidation reactions were carried out under aqueous environment, however, in the absence of any extraneous base or co-catalyst. Sensitive/oxidizable functional groups like cyano, sulfide, hydroxyl, aryl-hydroxyl
    基于表面活性剂的氧二过氧络合物可以活化分子氧,已被用作催化剂,以控制苄基醇氧化为相应的羰基。氧化反应在性环境下进行,但是在没有任何无关的碱或助催化剂的情况下进行。在转化过程中可以耐受敏感/可氧化的官能团,例如基,硫化物,羟基,芳基-羟基,烯烃(内部/末端),炔烃(内部/末端)和乙缩醛。这种选择性归因于催化剂的温和性质。该方法还可以扩大规模以用于多克合成,并且该方案很可能会得到实际应用,因为它需要廉价的可回收催化剂和易于获得的氧化剂(在绿色条件下)。
  • NANOSTRUCTURED METALS
    申请人:Ying Jackie Y.
    公开号:US20120136164A1
    公开(公告)日:2012-05-31
    The invention relates to a nanoparticulate material comprising long ultrathin metal nanowires, and to processes for making it. The nanoparticulate material may be used as a catalyst and, in the presence of a chiral modifier, can catalyse enantioselective reactions.
    这项发明涉及一种包含长超薄属纳米线的纳米颗粒材料,以及制备该材料的方法。这种纳米颗粒材料可以用作催化剂,并在手性修饰剂的存在下,可以催化对映选择性反应。
  • [EN] SUBSTITUTED PYRAZOLES FFA4/GPR120 RECEPTOR AGONISTS<br/>[FR] PYRAZOLES SUBSTITUÉS AGONISTES DU RÉCEPTEUR FFA4/GPR120
    申请人:AXXAM SPA
    公开号:WO2019175152A1
    公开(公告)日:2019-09-19
    The present invention refers to compounds of formula (I) or a pharmaceutically acceptable salt thereof: Formula (I). These compounds have FFA4/GPR120 receptor (FFA4) agonistic properties. The invention refers also to pharmaceutical compositions comprising these compounds, chemical processes for preparing them and their use in the treatment or prophylaxis of diseases associated with FFA4 receptor activity in animals, in particular humans.
    本发明涉及式(I)的化合物或其药学上可接受的盐:式(I)。这些化合物具有FFA4/GPR120受体(FFA4)激动性特性。该发明还涉及包含这些化合物的药物组合物,用于制备它们的化学过程以及它们在治疗或预防与动物(特别是人类)FFA4受体活性相关的疾病中的用途。
  • Method For Producing Low Molecular Weight Aromatic Lignin-Derived Compounds
    申请人:CMBLU PROJEKT AG
    公开号:US20190085006A1
    公开(公告)日:2019-03-21
    The present invention relates to a method for producing one or more low molecular weight aromatic lignin-derived compounds. The method preferably comprises providing lignocellulosic material, subjecting the lignocellulosic material to a pulping process, separating pulp to provide a substantially pulp-free process stream comprising a modified lignin-derived component, isolating the modified lignin-derived component, subjecting the isolated modified lignin-derived component to a decomposition step comprising oxidative cracking (cracking and oxidizing) or reducing under the influence of a catalyst or electro-oxidation, and subjecting the resulting products to an isolation step, to provide a low molecular weight aromatic lignin-derived compound. Said compound may be further modified, e.g. by annulation. The inventive method preferably comprises further oxidizing said compound to a redox active compound. Additionally, the present invention relates to compounds obtainable by the inventive method and to an assembly for carrying out the inventive method. Furthermore, the present invention refers to a method for providing an existing pulp and/or paper manufacturing plant with said assembly.
    本发明涉及一种生产一种或多种低分子量芳香木质素衍生化合物的方法。该方法优选包括提供木质纤维素材料,将木质纤维素材料经过制浆过程,分离纸浆以提供含有改性木质素衍生组分的基本无纸浆过程流,分离改性木质素衍生组分,将分离的改性木质素衍生组分经过分解步骤,包括在催化剂或电氧化的影响下进行氧化裂解(裂解和氧化)或还原,然后将产生的产物经过隔离步骤,以提供一种低分子量芳香木质素衍生化合物。该化合物可以进一步通过环化等方式进行改性。该创新方法优选包括将该化合物进一步氧化为一种氧化还原活性化合物。此外,本发明涉及通过该创新方法获得的化合物以及用于执行该创新方法的装配。此外,本发明涉及一种用所述装配为现有的制浆和/或造纸制造工厂提供的方法。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫