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(5α)-pregnan-3-one | 14778-11-1

中文名称
——
中文别名
——
英文名称
(5α)-pregnan-3-one
英文别名
5α-Pregnan-3-on;5alpha-pregnan-3-one;Pregnan-3-one, (5alpha)-;(5S,8S,9S,10S,13R,14S,17S)-17-ethyl-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one
(5α)-pregnan-3-one化学式
CAS
14778-11-1
化学式
C21H34O
mdl
——
分子量
302.5
InChiKey
JMAPHBFIBIHSIT-PMJYHDSJSA-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):
    6.3
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    描述:
    (5α)-pregnan-3-one三氟乙酸2-碘酰基苯甲酸 作用下, 以 二甲基亚砜 为溶剂, 反应 17.0h, 以91%的产率得到5α-pregn-1-en-3-one
    参考文献:
    名称:
    Regioselective dehydrogenation of 3-keto-steroids to form conjugated enones using o-iodoxybenzoic acid and trifluoroacetic acid catalysis
    摘要:
    Mild and regioselective conversion of 3-keto-5 alpha- and 3-keto-5 beta-steroids (trans A/B- and cis A/B-ring juncture, respectively) to the corresponding enones (Delta(1)- and Delta(4)-3-ketones) by treatment with oiodoxybenzoic acid (IBX) catalyzed by trifluoroacetic acid (TFA) in DMSO, is described. The IBX-mediated reaction involved dehydrogenation of the alpha- and beta-hydrogen atoms of the 3-ketones to give the enones regioselectively in good isolated yields without concomitant formation of related dienones and trienones. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
    DOI:
    10.1016/j.chemphyslip.2013.11.007
  • 作为产物:
    描述:
    5α-pregnan-3β-olchromium(VI) oxide溶剂黄146 作用下, 以 氯仿 为溶剂, 生成 (5α)-pregnan-3-one
    参考文献:
    名称:
    梨形肉球菌生物碱C
    摘要:
    摘要 早先从梨形肉球菌中分离的生物碱 C 已被证明是 3 a -甲氧基-20 a -二甲氨基-孕-5-烯。
    DOI:
    10.1016/s0031-9422(00)94070-6
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文献信息

  • Reactions photochimiques d'amines tertiaires et d'alcaloides—III
    作者:D. Herlem、Y. Hubert-Brierre、F. Khuong-Huu、R. Goutarel
    DOI:10.1016/0040-4020(73)80164-4
    日期:1973.1
    Photo-oxidation reactions, sensitized by methylene blue, of various tertiary amines and alkaloids have been studied. An immonium ion is postulated as an intermediate in the formation of secondary amines and of some cyclization and dimerization products.
    已经研究了由亚甲基蓝敏化的各种叔胺和生物碱的光氧化反应。假定离子是仲胺形成以及某些环化和二聚产物中的中间体。
  • Facilitating Children's Understanding of Misinterpretation: Explanatory Efforts and Improvements in Perspective Taking
    作者:Bradford H. Pillow、Clay Mash、Samuel Aloian、Valerie Hill
    DOI:10.1080/00221320209598673
    日期:2002.6
    The authors investigated children's understanding of how mistaken beliefs can arise through misinterpretation of ambiguous information. Children (N = 91), aged 4 to 5 years, were given pre- and posttests on their ability to infer a puppet's interpretation of a restricted-view drawing after the puppet had been led to an erroneous expectation about the drawing's identity. Before the posttest, the children received either self-explanation training or other-explanation training in which they explained the source of their own or a puppet's misinterpretations of drawings; a control group received no training. The children who received training improved from pre- to posttest, and those who had practiced explaining misinterpretations by referring to previously viewed pictures or to features of a target picture showed the greatest improvement. These results indicate that learning to explain misinterpretations can help children recognize situations in which misinterpretations are likely to occur.
  • Janot,M.-M. et al., Bulletin de la Societe Chimique de France, 1961, p. 2109 - 2113
    作者:Janot,M.-M. et al.
    DOI:——
    日期:——
  • Über Steroide und Sexualhormone (58. Mitteilung) Umwandlung von 17-Äthinyl-androstendiol-(3,17) in Pregnadienol-(3)
    作者:L. Ruzicka、M. W. Goldberg、E. Hardegger
    DOI:10.1002/hlca.193902201165
    日期:——
  • Janot,M.-M. et al., Bulletin de la Societe Chimique de France, 1960, p. 1669 - 1673
    作者:Janot,M.-M. et al.
    DOI:——
    日期:——
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同类化合物

(5β)-17,20:20,21-双[亚甲基双(氧基)]孕烷-3-酮 (5α)-2′H-雄甾-2-烯并[3,2-c]吡唑-17-酮 (3β,20S)-4,4,20-三甲基-21-[[[三(异丙基)甲硅烷基]氧基]-孕烷-5-烯-3-醇-d6 (25S)-δ7-大发酸 (20R)-孕烯-4-烯-3,17,20-三醇 (11β,17β)-11-[4-({5-[(4,4,5,5,5-五氟戊基)磺酰基]戊基}氧基)苯基]雌二醇-1,3,5(10)-三烯-3,17-二醇 齐墩果酸衍生物1 黄麻属甙 黄芪皂苷III 黄芪皂苷 II 黄芪甲苷 IV 黄芪甲苷 黄肉楠碱 黄果茄甾醇 黄杨醇碱E 黄姜A 黄夹苷B 黄夹苷 黄夹次甙乙 黄夹次甙乙 黄夹次甙丙 黄体酮环20-(乙烯缩醛) 黄体酮杂质EPL 黄体酮杂质1 黄体酮杂质 黄体酮杂质 黄体酮EP杂质M 黄体酮EP杂质G(RRT≈2.53) 黄体酮EP杂质F 黄体酮6-半琥珀酸酯 黄体酮 17alpha-氢过氧化物 黄体酮 11-半琥珀酸酯 黄体酮 麦角甾醇葡萄糖苷 麦角甾醇氢琥珀酸盐 麦角甾烷-6-酮,2,3-环氧-22,23-二羟基-,(2b,3b,5a,22R,23R,24S)-(9CI) 麦角甾烷-3,6,8,15,16-五唑,28-[[2-O-(2,4-二-O-甲基-b-D-吡喃木糖基)-a-L-呋喃阿拉伯糖基]氧代]-,(3b,5a,6a,15b,16b,24x)-(9CI) 麦角甾烷-26-酸,5,6:24,25-二环氧-14,17,22-三羟基-1-羰基-,d-内酯,(5b,6b,14b,17a,22R,24S,25S)-(9CI) 麦角甾-8-烯-3-醇 麦角甾-8,24(28)-二烯-26-酸,7-羟基-4-甲基-3,11-二羰基-,(4a,5a,7b,25S)- 麦角甾-7,22-二烯-3-酮 麦角甾-7,22-二烯-17-醇-3-酮 麦角甾-5,24-二烯-26-酸,3-(b-D-吡喃葡萄糖氧基)-1,22,27-三羟基-,d-内酯,(1a,3b,22R)- 麦角甾-5,22,25-三烯-3-醇 麦角甾-4,6,8(14),22-四烯-3-酮 麦角甾-1,4-二烯-3-酮,7,24-二(乙酰氧基)-17,22-环氧-16,25-二羟基-,(7a,16b,22R)-(9CI) 麦角固醇 麦冬皂苷D 麦冬皂苷D 麦冬皂苷 B