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(3s)-3-(羟基甲基)-n-[(1s)-1-(1-萘)乙基]-4-戊烯酰胺 | 214976-90-6

中文名称
(3s)-3-(羟基甲基)-n-[(1s)-1-(1-萘)乙基]-4-戊烯酰胺
中文别名
——
英文名称
4-Pentenamide, 3-(hydroxymethyl)-N-[(1S)-1-(1-naphthalenyl)ethyl]-, (3S)-
英文别名
(3S)-3-(hydroxymethyl)-N-[(1S)-1-naphthalen-1-ylethyl]pent-4-enamide
(3s)-3-(羟基甲基)-n-[(1s)-1-(1-萘)乙基]-4-戊烯酰胺化学式
CAS
214976-90-6
化学式
C18H21NO2
mdl
——
分子量
283.37
InChiKey
ZNSWFZCGMQTFHD-UONOGXRCSA-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:
    527.1±50.0 °C(Predicted)
  • 密度:
    1?+-.0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    21
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (3s)-3-(羟基甲基)-n-[(1s)-1-(1-萘)乙基]-4-戊烯酰胺 在 palladium on activated charcoal 氢氧化钾氢气对甲苯磺酸 作用下, 以 乙醇乙二醇 为溶剂, 反应 10.17h, 生成 (R)-4-ethyldihydrofuran-2(3H)-one
    参考文献:
    名称:
    Synthesis and absolute configuration of the insecticidal sesquilignan (+)-HAEDOXAN a in honour of professor G. H. Neil Towers 75th birthday
    摘要:
    The insecticidal neolignan, (+)-haedoxan A, was synthesized from (S)-(+)-beta-vinyl-gamma-butyrolactone and (2R,3R)-(+)-6-formyl-7-methoxy-3-methoxymethyl-2-(3,4-methylenedioxyphenyl)-1,4-benzodioxane, and its absolute configuration was unequivocally established as 1S,2R,5R,6S,2"R,3''R. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0031-9422(98)00270-2
  • 作为产物:
    描述:
    4-乙烯基二氢呋喃-2(3H)-酮(S)-(-)-1-(1-萘基)乙胺2-羟基吡啶 作用下, 反应 10.0h, 以3.58 g的产率得到(3s)-3-(羟基甲基)-n-[(1s)-1-(1-萘)乙基]-4-戊烯酰胺
    参考文献:
    名称:
    Synthesis and absolute configuration of the insecticidal sesquilignan (+)-HAEDOXAN a in honour of professor G. H. Neil Towers 75th birthday
    摘要:
    The insecticidal neolignan, (+)-haedoxan A, was synthesized from (S)-(+)-beta-vinyl-gamma-butyrolactone and (2R,3R)-(+)-6-formyl-7-methoxy-3-methoxymethyl-2-(3,4-methylenedioxyphenyl)-1,4-benzodioxane, and its absolute configuration was unequivocally established as 1S,2R,5R,6S,2"R,3''R. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0031-9422(98)00270-2
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文献信息

  • Synthesis and absolute configuration of the insecticidal sesquilignan (+)-HAEDOXAN a in honour of professor G. H. Neil Towers 75th birthday
    作者:Fumito Ishibashi、Eiji Taniguchi
    DOI:10.1016/s0031-9422(98)00270-2
    日期:1998.9
    The insecticidal neolignan, (+)-haedoxan A, was synthesized from (S)-(+)-beta-vinyl-gamma-butyrolactone and (2R,3R)-(+)-6-formyl-7-methoxy-3-methoxymethyl-2-(3,4-methylenedioxyphenyl)-1,4-benzodioxane, and its absolute configuration was unequivocally established as 1S,2R,5R,6S,2"R,3''R. (C) 1998 Elsevier Science Ltd. All rights reserved.
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