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[(E,1S)-1-cyclohexylpentadec-4-en-2-ynyl] naphthalene-2-carboxylate | 1263786-24-8

中文名称
——
中文别名
——
英文名称
[(E,1S)-1-cyclohexylpentadec-4-en-2-ynyl] naphthalene-2-carboxylate
英文别名
——
[(E,1S)-1-cyclohexylpentadec-4-en-2-ynyl] naphthalene-2-carboxylate化学式
CAS
1263786-24-8
化学式
C32H42O2
mdl
——
分子量
458.684
InChiKey
BHKUYMCITNOTDC-LYJXMUGZSA-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):
    11.5
  • 重原子数:
    34
  • 可旋转键数:
    13
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    [(E,1S)-1-cyclohexylpentadec-4-en-2-ynyl] acetate 在 4-二甲氨基吡啶1,2-二氯乙烷 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 50.0h, 生成 [(E,1S)-1-cyclohexylpentadec-4-en-2-ynyl] naphthalene-2-carboxylate
    参考文献:
    名称:
    Faulknerynes A−C from a Bahamian Sponge Diplastrella sp.: Stereoassignment by Critical Application of Two Exciton Coupled CD Methods
    摘要:
    Long-chain polyacetylene alcohols, faulknerynes A-C, along with known compounds diplynes A, C and E, were isolated from two specimens of the encrusting sponge, Diplastrella sp., collected from the surface of coral in the Bahamas. Two CD methods were critically evaluated for their suitability to terminal propargylic glycols and applied to assignment of configurations of faulkneryne A and diplyne C.
    DOI:
    10.1021/jo102188q
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文献信息

  • Faulknerynes A−C from a Bahamian Sponge <i>Diplastrella</i> sp.: Stereoassignment by Critical Application of Two Exciton Coupled CD Methods
    作者:Jaeyoung Ko、Brandon I. Morinaka、Tadeusz F. Molinski
    DOI:10.1021/jo102188q
    日期:2011.2.4
    Long-chain polyacetylene alcohols, faulknerynes A-C, along with known compounds diplynes A, C and E, were isolated from two specimens of the encrusting sponge, Diplastrella sp., collected from the surface of coral in the Bahamas. Two CD methods were critically evaluated for their suitability to terminal propargylic glycols and applied to assignment of configurations of faulkneryne A and diplyne C.
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