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4aβ,5,6,7,8,8aα-hexahydro-2(1H)-naphthalenone | 2384-50-1

中文名称
——
中文别名
——
英文名称
4aβ,5,6,7,8,8aα-hexahydro-2(1H)-naphthalenone
英文别名
bicyclo(4.4.0)decene-4 one-3 trans;(+/-)-6-oxo-trans-1.2.3.4.4a.5.6.8a-octahydro-naphthalene;(+/-)-6-Oxo-trans-1.2.3.4.4a.5.6.8a-octahydro-naphthalin;2-Oxo-trans-1,2,4a,5,6,7,8,8a-octahydro-naphthalin;(+/-)-trans-Δ1-Octalon-(3);trans-Δ3-2-Decalon;(4aS,8aR)-4a,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one
4aβ,5,6,7,8,8aα-hexahydro-2(1H)-naphthalenone化学式
CAS
2384-50-1;18317-63-0;55999-54-7;71956-17-7
化学式
C10H14O
mdl
——
分子量
150.221
InChiKey
RZWOGVZREQGWCL-RKDXNWHRSA-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

  • 沸点:
    125-128 °C(Press: 14 Torr)
  • 密度:
    1.013±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2914299000

SDS

SDS:f669b0278cafe1335148206a29313e7f
查看

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

反应信息

  • 作为反应物:
    描述:
    4aβ,5,6,7,8,8aα-hexahydro-2(1H)-naphthalenoneplatinum(IV) oxide 三氯化铝氢气 作用下, 以 乙醇 为溶剂, 25.0~40.0 ℃ 、101.33 kPa 条件下, 反应 9.67h, 生成 1α-methyl-1,2,3,4,4aβ,4bβ,5,6,7,8,8aα,10aβ-dodecahydro-10(9H)-phenanthrenone
    参考文献:
    名称:
    Diels-Alder reactions of cycloalkenones. 12. Reaction of trans-.DELTA.1,2-3-octalone with (E)-piperylene
    摘要:
    DOI:
    10.1021/jo00242a015
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 硫酸 作用下, 生成 4aβ,5,6,7,8,8aα-hexahydro-2(1H)-naphthalenone
    参考文献:
    名称:
    Lehmann; Kraetschell, Chemische Berichte, 1934, vol. 67, p. 1867,1868
    摘要:
    DOI:
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文献信息

  • Improved Dienophilicity of Nitrocycloalkenes: Prospects for the Development of a <i>trans</i>-Diels−Alder Paradigm
    作者:Woo Han Kim、Jun Hee Lee、Samuel J. Danishefsky
    DOI:10.1021/ja9058926
    日期:2009.9.9
    The development of an efficient and stereoselective trans-Diels-Alder paradigm is described. A central element of this transformation is the introduction of a temporary dienophilic functionality (A), which serves both to activate the substrate for Diels-Alder cycloaddtion and, through its subsequent removal, to facilitate conversion of the cis-fused cycloadducts to the trans-fused series.
    描述了一种高效和立体选择性的 trans-Diels-Alder 范式的发展。这种转变的一个核心要素是引入了一个临时的亲双烯官能团 (A),它既可以激活 Diels-Alder 环加成的底物,又可以通过随后的去除促进顺式稠合环加成物转化为反式-融合系列。
  • Über cyclische β-Diketone. 3. Mitteilung. Die Methylierung von (±)-<i>cis</i>- und (±)-<i>trans</i>-Decalindion-(1,3), sowie von (±)-2-Methyl-<i>trans</i>-decalindion-(1,3) mit Diazomethan
    作者:H. Mühle、Ch. Tamm
    DOI:10.1002/hlca.19620450513
    日期:——
    (±)-trans-decalin-1, 3-dione (V) yields (±)-3-methoxy-trans-Δ2-octalin-1-one (VII) and (±)-1-methoxy-trans-Δ1-octalin-3-one (IX) in a ratio of 2:1. Methylation in the cis-series gives the analogous products XVI and XVIII in the same ratio. The structure of the four isomeric enol-methylethers VII, IX, XVI and XVIII is proven by their conversion into the corresponding α,β-unsaturated octalenones and the saturated
    上用乙醚-甲醇重氮甲烷(在202小时°)处理,(±) -反式-decalin-1,-1,3-二酮(V)的产率的(±)-3-甲氧基反式-Δ 2 -octalin -1-酮(VII)和(±)-1-甲氧基-反式-Δ 1 -octalin -3-酮(IX)中的2:1的比例。顺式系列的甲基化以相同的比例得到类似的产物XVI和XVIII。四个异构的烯醇甲基醚VII,IX,XVI和XVIII的结构通过将其转化为相应的α,β-不饱和八烯酮和饱和十酮而得到证明。
  • 4-(Substituted phenyl)-naphthalen-2(1H)-ones and 2-ols, processes for their preparation, and pharmaceutical compositions containing them
    申请人:PFIZER INC.
    公开号:EP0049953A2
    公开(公告)日:1982-04-21
    Compounds having the formula wherein A when taken individually is hydrogen; B when taken individually is hydroxy or alkanoyloxy having from one to five carbon atoms; A and B when taken together are oxo; R, is hydrogen, benzyl, or R1' wherein R1' is alkanoyl having from one to five carbon atoms, P(O) (OH)2 and mono-and disodium and potassium salts thereof, -CO(CH2)2COOH and the sodium and potassium salts thereof, or -CO(CH2)pNR4R5 wherein p is 0 or an integer from 1 to 4, each of R4 and R5 when taken individually is hydrogen or alkyl having from one to four carbon atoms; R4 and R5 when taken together with the nitrogen to which they are attached are piperidino, pyrrolo, pyrrolidino, morpholino or N-alkylpiperazino having from one to four carbon atoms in the alkyl group; R2 when taken individually is hydrogen; R3 when taken individually is hydrogen, methyl, hydroxy, hydroxymethyl, -OR,' or -CH2OR1'; R2 and R3 when taken together are oxo, methylene or alkylenedioxy having from two to four carbon atoms; W is hydrogen, pyridyl, or wherein W, is hydrogen, chloro or fluoro; when W is hydrogen, Z is (a) alkylene having from five to thirteen carbon atoms; or (b) -lalk1)m-O-(alk2)n- wherein each of (alk,) and (alk2) is alkylene having from one to thirteen carbon atoms; each of m and n is 0 or 1; with the provisos that the summation of carbon atoms in (alk1) plus (alk2) is not less than five or greater than thirteen; and at least one of m and n is 1; when W is other than hydrogen, Z is (a) alkylene having from three to eight carbon atoms; or (b) -(elk1)m-O-(alk2)n- wherein each of (alk1) and (alk2) is alkylene having from one to eight carbon atoms; each of m and n is 0 or 1; with the provisos that the summation of carbon atoms in (alk,) plus (alk2) is not less than three or greater than eight; and at least one of m and n is 1; or a pharmaceutically acceptable acid addition salt of those compounds wherein R, is -CO(CH2)pNR4R5 and/or W is pyridyl; pharmaceutical compositions containing them, and processes for their preparation. The compounds are particularly useful in the treatment of nausea and as analgesics.
    具有以下式子的化合物 其中 A 单独取值时为氢;B 单独取值时为具有 1 至 5 个碳原子的羟基或烷酰氧基; A 和 B 合在一起时为氧代; R,是氢、苄基或 R1',其中 R1'是具有 1 至 5 个碳原子的烷酰基、P(O) (OH)2 及其单钠盐、二钠盐和盐、-CO(CH2)2COOH 及其钠盐和盐,或-CO( )pNR4R5,其中 p 是 0 或 1 至 4 的整数,R4 和 R5 单独使用时各自是氢或具有 1 至 4 个碳原子的烷基;R4 和 R5 与它们所连接的氮一起为哌啶基吡咯基、吡咯烷基、吗啉基或 N-烷基哌嗪基,烷基中含有 1 至 4 个碳原子; R2 单独使用时为氢 R3 单独为氢、甲基、羟基、羟甲基、-OR、'或- OR1';R2 和 R3 合在一起为具有 2 至 4 个碳原子的氧代、亚甲基或亚烷基二氧基; W 是氢、吡啶基或 其中 W 是氢、; 当 W 是氢时,Z 是 (a) 具有 5 至 13 个碳原子的亚烷基;或 (b) -lalk1)m-O-(alk2)n- 其中(alk,)和(alk2)各自为具有一至十三个碳原子的亚烷基;m 和 n 各自为 0 或 1;但前提是(alk1)和(alk2)中碳原子的总和不小于五个或大于十三个;且 m 和 n 中至少有一个为 1; 当 W 不是氢时,Z 是 (a) 具有三至八个碳原子的亚烷基;或 (b) -(elk1)m-O-(alk2)n- 其中(alk1)和(alk2)各为具有 1 至 8 个碳原子的亚烷基;m 和 n 各为 0 或 1;但前提是(alk,)加(alk2)中碳原子的总和不小于 3 或大于 8;且 m 和 n 中至少有一个为 1; 或这些化合物的药学上可接受的酸加成盐,其中 R, 是-CO( )pNR4R5 和/或 W 是吡啶基;含有这些化合物的药物组合物及其制备工艺。这些化合物特别适用于治疗恶心和镇痛。
  • Synthesis of .gamma.-dimethylaminomethyl-.alpha.-phenylcycloalkyl propionates as potential analgetics
    作者:Mathias P. Mertes、Arthur A. Ramsey、Patrick E. Hanna、Duane D. Miller
    DOI:10.1021/jm00299a001
    日期:1970.9
  • Potin,P.; Wylde,R., Bulletin de la Societe Chimique de France, 1967, p. 4445 - 4453
    作者:Potin,P.、Wylde,R.
    DOI:——
    日期:——
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