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3β-hydroxy-5-methyl-19-nor-5β,9β,10β-androstan-17β-yl cyclohexanecarboxylate | 402713-59-1

中文名称
——
中文别名
——
英文名称
3β-hydroxy-5-methyl-19-nor-5β,9β,10β-androstan-17β-yl cyclohexanecarboxylate
英文别名
——
3β-hydroxy-5-methyl-19-nor-5β,9β,10β-androstan-17β-yl cyclohexanecarboxylate化学式
CAS
402713-59-1
化学式
C26H42O3
mdl
——
分子量
402.618
InChiKey
GVFQWRVDZIYLHV-SFESNHAHSA-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

反应信息

  • 作为反应物:
    描述:
    3β-hydroxy-5-methyl-19-nor-5β,9β,10β-androstan-17β-yl cyclohexanecarboxylate 在 jones reagent 作用下, 以 丙酮 为溶剂, 反应 0.17h, 以91%的产率得到3-oxo-5-methyl-19-nor-5β,9β,10β-androstan-17β-yl cyclohexanecarboxylate
    参考文献:
    名称:
    Analogues of androgen hormones with inverted configuration at carbons 5, 9, and 10
    摘要:
    On catalytic hydrogenation of Delta (9)-steroids (e.g. 3 beta -hydroxy-5-methyl-19-nor-5 beta -androst-9-en-17-one), four isomers were formed: 9 alpha ,10 alpha-, 9 alpha ,10 beta-, 9 beta ,10 alpha- and 9 beta ,10 beta -adducts. The product distribution was affected by the nature of the C-3 substituent. A chair conformation of A, B, and C rings was found in all of the products with the exception of the 9 alpha ,10 alpha -adduct whose B ring adopts a twist boat conformation. The products were utilized for the synthesis of dihydrotestosterone analogues. (C) 2002 Elsevier Science Inc. All rights reserved.
    DOI:
    10.1016/s0039-128x(01)00135-0
  • 作为产物:
    描述:
    5-methyl-19-nor-3-oxo-5β-androst-9-en-17β-yl benzoate 在 platinum(IV) oxide sodium tetrahydroborate 、 氢气 作用下, 以 乙醇二氯甲烷溶剂黄146 为溶剂, 反应 19.0h, 生成 3β-hydroxy-5-methyl-19-nor-5β,9β,10β-androstan-17β-yl cyclohexanecarboxylate
    参考文献:
    名称:
    Analogues of androgen hormones with inverted configuration at carbons 5, 9, and 10
    摘要:
    On catalytic hydrogenation of Delta (9)-steroids (e.g. 3 beta -hydroxy-5-methyl-19-nor-5 beta -androst-9-en-17-one), four isomers were formed: 9 alpha ,10 alpha-, 9 alpha ,10 beta-, 9 beta ,10 alpha- and 9 beta ,10 beta -adducts. The product distribution was affected by the nature of the C-3 substituent. A chair conformation of A, B, and C rings was found in all of the products with the exception of the 9 alpha ,10 alpha -adduct whose B ring adopts a twist boat conformation. The products were utilized for the synthesis of dihydrotestosterone analogues. (C) 2002 Elsevier Science Inc. All rights reserved.
    DOI:
    10.1016/s0039-128x(01)00135-0
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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