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4α,24β-dimethyl-5α-cholest-22E-en-3β-ol | 77982-80-0

中文名称
——
中文别名
——
英文名称
4α,24β-dimethyl-5α-cholest-22E-en-3β-ol
英文别名
4α,24R-dimethyl-5α-cholest-22E-en-3β-ol;4α-24R-dimethyl-5α-cholest-22-en-3β-ol;(24R)-4α,24-dimethyl-22-dehydrocholestanol;(3S,4S,5S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-4,10,13-trimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
4α,24β-dimethyl-5α-cholest-22E-en-3β-ol化学式
CAS
77982-80-0
化学式
C29H50O
mdl
——
分子量
414.715
InChiKey
DGJHBFBQAQKVKB-GSQFFBPDSA-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):
    9.3
  • 重原子数:
    30
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 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:
    描述:
    4α,24β-dimethyl-5α-cholest-22E-en-3β-ol 在 palladium on activated charcoal 氢气 作用下, 以 甲醇 为溶剂, 生成 4α,24β-dimethyl-5α-cholestan-3β-ol
    参考文献:
    名称:
    Marine Sterols X.★★Part IX, Kobayashi, M., Hayashi, T., Nakajima, F., and Mitsuhashi, H., STEROIDS, 34, 285 (1979). minor constituents of the sterols of the soft coral Sarcophyton glaucum
    摘要:
    DOI:
    10.1016/0039-128x(82)90034-4
  • 作为产物:
    参考文献:
    名称:
    Marine 4-methyl sterols: Synthesis of C-24 epimers of 4α,24-dimethyl-5α-cholestan-3β-OL and 360 MHz 1HNMR comparisons to the natural product from Plexaura homomalla
    摘要:
    Comparison of the highfield 1HNMR spectrum of 4 alpha, 24-dimethyl-5 alpha-cholestan-3 beta-o1 isolated by open column adsorptive chromatography and reversed-phase HPLC from P. homomalla with those of the corresponding synthetic 24 alpha and 24 beta compounds demonstrate that the gorgonian natural product is purely 24 beta, the same C-24 configuration found in sterols related to dinosterol and gorgosterol. 360 MHz 1HNMR data are also reported for synthetic 4 alpha, 24 beta-dimethyl-5 alpha-cholest-22E-en-3 beta-o1 (another P. homomalla natural product). The use of 1HNMR correlations in assigning C-24 configurations of 24-methyl marine sterols possessing various nuclei is examined and discussed. Analyses of the methyl sterol components of P. homomalla are tabulated and discussed with regard to origin and plausible biosynthetic interrelationships in light of the C-24 configurational findings.
    DOI:
    10.1016/s0039-128x(83)90220-9
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文献信息

  • Identification and complete spectral assignment for two 4?-methylsterols in an inseparable mixture using 2D NMR
    作者:William F. Reynolds、Stewart McLean、Haydelba T. D'Armas、Baldwin S. Mootoo
    DOI:10.1002/1097-458x(200102)39:2<94::aid-mrc793>3.0.co;2-c
    日期:2001.2
  • Marine 4-methyl sterols: Synthesis of C-24 epimers of 4α,24-dimethyl-5α-cholestan-3β-OL and 360 MHz 1HNMR comparisons to the natural product from Plexaura homomalla
    作者:W.C. Dow、T. Gebreyesus、S. Popov、R.M.K. Carlson、Carl Djerassi
    DOI:10.1016/s0039-128x(83)90220-9
    日期:1983.8
    Comparison of the highfield 1HNMR spectrum of 4 alpha, 24-dimethyl-5 alpha-cholestan-3 beta-o1 isolated by open column adsorptive chromatography and reversed-phase HPLC from P. homomalla with those of the corresponding synthetic 24 alpha and 24 beta compounds demonstrate that the gorgonian natural product is purely 24 beta, the same C-24 configuration found in sterols related to dinosterol and gorgosterol. 360 MHz 1HNMR data are also reported for synthetic 4 alpha, 24 beta-dimethyl-5 alpha-cholest-22E-en-3 beta-o1 (another P. homomalla natural product). The use of 1HNMR correlations in assigning C-24 configurations of 24-methyl marine sterols possessing various nuclei is examined and discussed. Analyses of the methyl sterol components of P. homomalla are tabulated and discussed with regard to origin and plausible biosynthetic interrelationships in light of the C-24 configurational findings.
  • Marine Sterols X.★★Part IX, Kobayashi, M., Hayashi, T., Nakajima, F., and Mitsuhashi, H., STEROIDS, 34, 285 (1979). minor constituents of the sterols of the soft coral Sarcophyton glaucum
    作者:Masaru Kobayashi、Takashi Ishizaka、Hiroshi Mitsuhashi
    DOI:10.1016/0039-128x(82)90034-4
    日期:1982.8
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