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(E)-3-(3-(adamantan-1-yl)-4-benzyloxyphenyl)prop-2-en-1-ol | 932017-94-2

中文名称
——
中文别名
——
英文名称
(E)-3-(3-(adamantan-1-yl)-4-benzyloxyphenyl)prop-2-en-1-ol
英文别名
(E)-3-[3-(1-adamantyl)-4-phenylmethoxyphenyl]prop-2-en-1-ol
(E)-3-(3-(adamantan-1-yl)-4-benzyloxyphenyl)prop-2-en-1-ol化学式
CAS
932017-94-2
化学式
C26H30O2
mdl
——
分子量
374.523
InChiKey
JNQNKMUGFAZFFQ-QPJJXVBHSA-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):
    6.5
  • 重原子数:
    28
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 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
  • 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:
    New synthetic approach to atypical retinoids: application of a versatile annulation procedure
    摘要:
    A new approach to an atypical retinoid is presented. The C-15 skeleton was built up by exploiting a step-by-step sequence: the C-9 fragment of an intermediate was homologated by reaction with a C-4 phosphorane, and then submitted to a benzannulation reaction. The last two carbon atoms were inserted by a Wittig reaction with the C-2 phosphorane of ethyl bromoacetate. Manipulation of functional groups was then performed. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.12.038
  • 作为产物:
    描述:
    参考文献:
    名称:
    New synthetic approach to atypical retinoids: application of a versatile annulation procedure
    摘要:
    A new approach to an atypical retinoid is presented. The C-15 skeleton was built up by exploiting a step-by-step sequence: the C-9 fragment of an intermediate was homologated by reaction with a C-4 phosphorane, and then submitted to a benzannulation reaction. The last two carbon atoms were inserted by a Wittig reaction with the C-2 phosphorane of ethyl bromoacetate. Manipulation of functional groups was then performed. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.12.038
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文献信息

  • New synthetic approach to atypical retinoids: application of a versatile annulation procedure
    作者:Elisabetta Brenna、Claudio Fuganti、Giovanni Fronza、Francesco G. Gatti、Federico Sala、Stefano Serra
    DOI:10.1016/j.tet.2006.12.038
    日期:2007.3
    A new approach to an atypical retinoid is presented. The C-15 skeleton was built up by exploiting a step-by-step sequence: the C-9 fragment of an intermediate was homologated by reaction with a C-4 phosphorane, and then submitted to a benzannulation reaction. The last two carbon atoms were inserted by a Wittig reaction with the C-2 phosphorane of ethyl bromoacetate. Manipulation of functional groups was then performed. (c) 2007 Elsevier Ltd. All rights reserved.
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同类化合物

(R)-斯替戊喷酯-d9 隐甲藻 苯酚,2-(1-氯-3-乙基-3-羟基-1-戊烯基)-,(E)- 苯甲醛甘油缩醛 苯(甲)醛,2-[(1E,3S,4S,5E)-3,4-二羟基-1,5-庚二烯-1-基]-6-羟基- 肉桂醇 稻瘟醇 烯效唑 烯效唑 烯唑醇 (E)-(S)-异构体 氯化2-[(4-氨基-2-氯苯基)偶氮]-1,3-二甲基-1H-咪唑正离子 戊基肉桂醇 咖啡酰基乙醇 反式-3,4,5-三甲氧基肉桂醇 alpha-苯乙烯基-4-吡啶甲醇 R-烯效唑 R-烯唑醇 6-甲基-1-(3,4-亚甲二氧基苯基)-1-庚烯-3-醇 5-甲基-1-(3,4,5-三甲氧基苯基)-1-己烯-3-醇 5-甲基-1-(1,3-苯并二氧戊环-5-基)-1-己烯-3-醇 4-苯基-3-丁烯-2-醇 4-羟基肉桂醇 4-羟基-6-苯基己-5-烯-2-酮 4-硝基肉桂醇 4-甲基-1-苯基戊-1-烯-3-醇 4-(4-硝基苯基)丁-3-烯-2-醇 4-(4-溴苯基)丁-3-烯-2-醇 4-(4,4-二甲基-3-羟基-1-戊烯基)邻苯二酚 4-(3-羟基丙烯基)-2,6-双(3-甲基-2-丁烯基)苯酚 4-(3-羟基丙-1-烯基)苯酚 4-(2-苯基乙烯基)庚-1,6-二烯-4-醇 4,4-二氯-5,5,5-三氟-1-苯基戊-1-烯-3-醇 4,4,5,5,5-五氟-1-苯基戊-1-烯-3-醇 3-苯基戊-2-烯-1,5-二醇 3-苯基丙-2-烯-1-醇 3-甲基肉桂醇 3-甲基-4-苯基丁-3-烯-2-醇 3-甲基-4-苯基丁-3-烯-1,2-二醇 3-甲基-1-苯基戊-1-烯-4-炔-3-醇 3-甲基-1-苯基戊-1-烯-3-醇 3-氯-4-氟-4-苯基丁-3-烯-2-醇 3-(4-甲基苯基)丙-2-烯-1-醇乙酸酯 3-(4-溴苯基)丙-2-烯-1-醇 3-(3-硝基苯基)丙-2-烯-1-醇 3-(3,5-二氟苯基)丙醇 3-(3,4-二氯苯基)丙-2-烯-1-醇 3-(3,4,5-三甲氧基苯基)-2-丙烯-1-醇 3-(2-溴苯基)丙-2-烯-1-醇 3-(2-氟苯基)丙-2-烯-1-醇 3-(2,4-二氯苯基)-2-丙烯-1-醇