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17β-acetoxy-3,3-ethanediyldioxy-androst-5-ene | 6173-28-0

中文名称
——
中文别名
——
英文名称
17β-acetoxy-3,3-ethanediyldioxy-androst-5-ene
英文别名
17β-Acetoxy-3,3-aethandiyldioxy-androst-5-en;[(8R,9S,10R,13S,14S,17S)-10,13-dimethylspiro[1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,2'-1,3-dioxolane]-17-yl] acetate
17β-acetoxy-3,3-ethanediyldioxy-androst-5-ene化学式
CAS
6173-28-0
化学式
C23H34O4
mdl
——
分子量
374.521
InChiKey
JVXLQGKEDVFQKL-WLNPFYQQSA-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

  • 熔点:
    203-205 °C
  • 沸点:
    467.3±45.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.87
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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

点击查看最新优质反应信息

文献信息

  • Synthesis and characterization by 1H and 13C nuclear magnetic resonance spectroscopy of 17α-cyano, 17α-aminomethyl, and 17α-alkylamidomethyl derivatives of 5α-dihydrotestosterone and testosterone
    作者:Elisabeth Mappus、Christophe Chambon、Marc Rolland de Ravel、Catherine Grenot、Claude Y. Cuilleron
    DOI:10.1016/s0039-128x(97)00046-9
    日期:1997.8
    17 alpha-Aminomethyl, 17 alpha-acetamidomethyl, and 17 alpha-hemiglutaramidomethyl derivatives of dihydrotestosterone and testosterone have been prepared by hydrocyanation of 3,3'-(ethylenedioxy)-5 alpha-androstan-17-one and 3,3'-ethylenedioxyandrost-5-en-17-one, reduction of the corresponding acetylated 17 alpha-cyanohydrins with lithium aluminium hydride, and acylation of the resulting 17 alpha-aminomethyl
    二氢睾丸激素睾丸激素的17α-基甲基,17α-乙酰基甲基和17α-半谷酰胺甲基衍生物已通过3,3'-(乙撑二氧基)-5α-雄烷-17-和3,3'-乙撑二氧基雄烷的氢化反应制得-5--1-17,用氢化铝锂还原相应的乙酰化的17α-醇,并用乙酸酐戊二酸单甲酯的单酰酰化所得的17个α-基甲基衍生物。皂化17种α-半戊二酰胺基甲基甲酯可得到相应的半戊酰胺基衍生物,而酸解17种α-乙酰酰胺基甲基和17种α-半戊二酰胺基甲基衍生物的3-乙烯缩酮可再生3-氧代和3-氧代-4-烯功能。通过1H和13C NMR确定了17个取代的类固醇的17α-构型,并通过与17个α-和17个β-基-17-羟基和4-4-烯-3-酮,17个β-基的NMR数据进行比较来确认具有已知17-构型的二氢睾丸激素睾丸激素的-3,3'-(亚乙二氧基)androst-5-en-17-ol,17α-炔基和17α-己酸
  • Steroids—CXX synthesis of halogenated steroid hormones
    作者:A. Bowers、L. Cuéllar Ibáñez、H.J. Ringold
    DOI:10.1016/0040-4020(59)80061-2
    日期:1959.1
    The conformational and electronic factors involved in the fission of steroid 5α,6α-epoxides with boron trifluoride-etherate are discussed with particular reference to C-3-keto-5α,6α-epoxides and their cycloethylene-dioxy derivatives.
    讨论了类固醇5α,6α-环氧化合物与三氟化硼-醚化物的裂变所涉及的构象和电子因素,特别是涉及C-3-酮5α,6α-环氧化合物及其环乙二氧基衍生物
  • 7-Keto Steroids. I. Steroidal 3-Hydroxy-3,5-dien-7-ones
    作者:C. W. Marshall、Richard E. Ray、Ivar Laos、Byron Riegel
    DOI:10.1021/ja01580a051
    日期:1957.12
  • A selectivity study of activated ketal reduction with borane dimethyl sulfide
    作者:Birgit Bartels、Roger Hunter
    DOI:10.1021/jo00076a041
    日期:1993.11
    A chemo- and regioselectivity study of the reagent combination BH3.SMe2/TMSOTf for ketal reduction has been undertaken. It has revealed that simple 1,3-dioxanes reduce cleanly at low temperature in CH2Cl2 while simple 1,3-dioxolanes may give complete ring cleavage and dimerization products. A study of reduction of 4-substituted 1,3-dioxolanes has revealed a solvent-directed regioselectivity which in THF favors the secondary protected derivative. A mechanism is postulated to account for the selectivities based on recent thinking on acetal substitution reactions.
  • Preparation of dehydroepiandrosterone, testosterone and progesterone antigens through 7-carboxymethyl derivatives: Characteristics of the antisera to testosterone and progesterone
    作者:Danièle Duval、Bernard Desfosses、Romeo Emiliozzi
    DOI:10.1016/0039-128x(80)90037-9
    日期:1980.3
    Dehydroepiandrosterone, testosterone and progesterone 7-carboxymethyl derivatives were prepared: 7 alpha and 7 beta epimers were separated and coupled to bovine serum albumin. Preliminary studies of the antisera induced by these antigens showed that they have high affinity and good specificity.
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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