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1-(2-hydroxy-4-methoxyphenyl)-2-phenylpropan-1-one | 76856-80-9

中文名称
——
中文别名
——
英文名称
1-(2-hydroxy-4-methoxyphenyl)-2-phenylpropan-1-one
英文别名
2-hydroxy-4-methoxy-α-C-methyldesoxybenzoin;1-(2-Hydroxy-4-methoxyphenyl)-2-phenyl-1-propanon
1-(2-hydroxy-4-methoxyphenyl)-2-phenylpropan-1-one化学式
CAS
76856-80-9
化学式
C16H16O3
mdl
——
分子量
256.301
InChiKey
ZRCQQAWNWIVUGI-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

  • 熔点:
    108 °C(Solv: ethanol (64-17-5))
  • 沸点:
    415.7±30.0 °C(Predicted)
  • 密度:
    1.157±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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-(2-hydroxy-4-methoxyphenyl)-2-phenylpropan-1-one 生成 2,4-dimethoxy-α-C-methyldesoxybenzoin
    参考文献:
    名称:
    JAIN, A. C.;PALIWAL, POONAM, INDIAN J. CHEM. B, 27,(1988) N1, C. 985-988
    摘要:
    DOI:
  • 作为产物:
    描述:
    7-甲氧基异黄酮lithium 作用下, 以 为溶剂, 以65%的产率得到1-(2-hydroxy-4-methoxyphenyl)-2-phenylpropan-1-one
    参考文献:
    名称:
    Major, A.; Nagy, Z.; Nogradi, M., Acta Chimica Academiae Scientiarum Hungaricae, 1980, vol. 104, p. 85 - 88
    摘要:
    DOI:
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文献信息

  • Synthesis of 2-Acylphenol and Flavene Derivatives from the Ruthenium-Catalyzed Oxidative C-H Acylation of Phenols with Aldehydes
    作者:Hanbin Lee、Chae S. Yi
    DOI:10.1002/ejoc.201403518
    日期:2015.3
    [(C6H6)(PCy3)(CO)RuH]+BF4- has been found to be an effective catalyst for the oxidative C-H coupling reaction of phenols with aldehydes to give 2-acylphenol compounds. The coupling of phenols with α,β-unsaturated aldehydes selectively gives the flavene derivatives. The catalytic method mediates direct oxidative C-H coupling of phenol and aldehyde substrates without using any metal oxidants or forming wasteful byproducts
    已发现阳离子氢化钌络合物 [(C6H6)(PCy3)(CO)RuH]+BF4- 是苯酚与醛的氧化 CH 偶联反应生成 2-酰基苯酚化合物的有效催化剂。酚与α,β-不饱和醛的偶联选择性地产生黄酮衍生物。该催化方法介导苯酚和醛底物的直接氧化 CH 偶联,而不使用任何金属氧化剂或形成浪费的副产物。
  • Synthesis of α-methyldeoxybenzoins
    作者:A. Salakka、K. Wähälä
    DOI:10.1039/a904946k
    日期:——
    methoxy-substituted isoflavones using LiAlH4 in refluxing THF provides an easy access to a number of α-methyldeoxybenzoins, possible metabolites of phytoestrogens in man. The synthesis of O-demethylangolensin 2b, 6′-hydroxyangolensin 2c, angolensin 2d, 1-(2,4-dihydroxyphenyl)-2-phenylpropan-1-one 2e, 1-(2-hydroxy-4-methoxyphenyl)-2-(4-hydroxyphenyl)propan-1-one 2f, 4′-O-methylangolensin 2g, 1-(2-hydroxy-4-metho
    在回流的THF中使用LiAlH 4还原羟基和/或甲氧基取代的异黄酮,可轻松获得大量α-甲基脱氧安息香素,可能是人体植物雌激素的代谢产物。的合成Ô -demethylangolensin 2b中,6'- hydroxyangolensin 2C,2D angolensin,1-(2,4-二羟基苯基)-2-苯基丙-1-酮2E,1-(2-羟基-4-甲氧基苯基)-2- (4-羟基苯基)丙烷-1-酮2f,4'- O-甲基血管紧张素2g,1-(2-羟基-4-甲氧基苯基)-2-苯基丙烷-1-酮2h和1-(2-羟基苯基)-描述了2-苯基丙烷-1-酮2i。
  • Major, A.; Nagy, Z.; Nogradi, M., Acta Chimica Academiae Scientiarum Hungaricae, 1980, vol. 104, p. 85 - 88
    作者:Major, A.、Nagy, Z.、Nogradi, M.
    DOI:——
    日期:——
  • Jain, A. C.; Paliwal, Poonam, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1988, vol. 27, # 1-12, p. 985 - 988
    作者:Jain, A. C.、Paliwal, Poonam
    DOI:——
    日期:——
  • MAJOR A.; NAGY Z.; NOGRADI M., ACTA CHIM. ACAD. SCI. HUNG., 1980, 104, NO 1, 85-87
    作者:MAJOR A.、 NAGY Z.、 NOGRADI M.
    DOI:——
    日期:——
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同类化合物

安哥拉紫檀素 2-羟基-3-苯基苯丙酮 1-(2,4-二羟基苯基-3,5-d2)-2-(4-羟基苯基-3,5-d2)丙烷-1-酮-2-d1 1-(2,4-二羟基苯基)-2-(4-羟基苯基)丙-1-酮 1-(1-羟基萘-2-基)-2-甲基-2-苯基丙烷-1-酮 1-(2-hydroxy-5-methylphenyl)-3-(naphthalen-1-yl)-2-phenylpropan-1-one 2,4,5,4'-tetramethoxy-α-methyldesoxybenzoin 1-[2-(1-hydroxynaphthyl)]-2-phenyl-1-propanone 1-(4-(cyc lohexyloxy)-2-methoxyphenyl)-2-(3,4-dimethoxyphenyl)propan-1-one 2-(3,4-dimethoxyphenyl)-1-(4-hydroxy-2-methoxyphenyl)propan-1-one 1-(2-Hydroxy-4-methoxyphenyl)-2-(4-hydroxyphenyl)propan-1-one 1-(2-methoxyphenyl)-2-phenylpropan-1-one 2-(2-fluorophenyl)-1-(2-methoxy-4-(piperidin-1-yl)phenyl)propan-1-one (-)-angolensin (-)-angolensin-4-methyl ether 1-(2-methoxyphenyl)-2-phenyl-2-(trimethylsilyloxy)propan-1-one 1-(2,5-dimethoxy-4-methylphenyl)-2-phenylpropan-1-one (+/-)-1-<2,5-Dimethyl-phenyl>-2-phenyl-propan-1-on 1-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)-[1,2,3-(13)C3]propan-1-one 1,2-bis(2-hydroxybenzoyl)-1-propanone 2-(3,4-dimethoxyphenyl)-1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl)-2-methylpropan-1-one (+/-)-2-<2,4-Bis(methoxymethoxy)phenyl>-1-<2-hydroxy-4-(methoxymethoxy)phenyl>propan-1-on 1-(2-hydroxyphenyl)-2-(4-methoxyphenyl)propan-1-one 1-(2,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-2-methylpropan-1-one 1-(2-hydroxy-4-methoxyphenyl)-2-(4-methoxyphenyl)-2-methylpropan-1-one 1-(2-hydroxy-4-methoxyphenyl)-2-phenylpropan-1-one 1-(2-hydroxyphenyl)-2-(2-hydroxy-4-methoxyphenyl)-1-propanone 2-hydroxy-3,4-dimethoxy-α-C-methoxydesoxybenzoin (R)-2-(3,4-dimethoxyphenyl)-1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl)propan-1-one 2-(3,4-dimethoxyphenyl)-1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl)propan-1-one 1-(2,5-dihydroxy-4-methoxyphenyl)-2-(4'-hydroxyphenyl)-1-propanone 1-(5-Bromo-2-hydroxyphenyl)-2-(2-nitrophenyl)propan-1-one 1-(2,5-dihydroxy-4-methoxyphenyl)-2-phenyl-1-propanone 1-(2,4-Dihydroxyphenyl)-2-phenylpropan-1-one 1-(2,3,4-trihydroxyphenyl)-2-phenyl-1-propanone (S)-2-(3,4-dimethoxyphenyl)-1-(5-methoxy-2,2-dimethyl-2H-chromen-6-yl)propan-1-one Ethyl 4-[1-[4-(dimethylamino)-2-hydroxyphenyl]-1-oxopropan-2-yl]benzoate 2-[[2-(2-Methyl-2-phenylpropanoyl)phenoxy]methoxy]propyl benzoate (2S)-1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)propan-1-one 1-[2,4-Bis(trimethylsiloxy)phenyl]-2-[(4-trimethylsiloxy)phenyl]propan-1-one 1-(2,4-dimethoxyphenyl)-2-(4-methoxyphenyl)propan-1-one (+/-)-Di-O-acetyl-angolensin 4'-hydroxy-2,4-dimethoxy-α-methyldeoxybenzoin 1-(2,3,4-dihydroxyphenyl)-2-(4'-hydroxyphenyl)-1-propanone 1-(2,4-Dihydroxyphenyl)-2-(3-hydroxy-4-methoxyphenyl)propan-1-one 2-(4-Methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one 1-(2,4-Dihydroxyphenyl)-2-(3,5-dimethoxyphenyl)propan-1-one 1-[4-[(1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-yl)oxy]-2-hydroxyphenyl]-2-(4-methoxyphenyl)propan-1-one 1-(2,4-Dihydroxy-5-methoxyphenyl)-2-(4-hydroxyphenyl)propan-1-one (+/-)-4-O-methylangolensin