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(4aR,4bS,8aS,8bR)-4a,4b-Diphenyl-dodecahydro-biphenylene | 72258-07-2

中文名称
——
中文别名
——
英文名称
(4aR,4bS,8aS,8bR)-4a,4b-Diphenyl-dodecahydro-biphenylene
英文别名
(4aR,4bS,8aS,8bR)-8a,8b-diphenyl-1,2,3,4,4a,4b,5,6,7,8-decahydrobiphenylene
(4aR,4bS,8aS,8bR)-4a,4b-Diphenyl-dodecahydro-biphenylene化学式
CAS
72258-07-2
化学式
C24H28
mdl
——
分子量
316.486
InChiKey
LPUHZRRLTWWWTG-NVPYSNMXSA-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):
    7.9
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

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文献信息

  • Photodimerization of 1-Phenylcyclohexene. A Novel Transient−Transient Component
    作者:David J. Unett、Richard A. Caldwell、Duane C. Hrncir
    DOI:10.1021/ja9533860
    日期:1996.1.1
    Low-temperature irradiations of 1-phenylcyclohexene (PC6) yield two singlet state 2 + 2 photodimers and two 4 + 2 cycloadducts. The 4 + 2 adducts are not observed in low intensity lamp irradiations at room temperature but are produced in significant quantities when PC6 solutions are subjected to higher intensity laser irradiation. The results indicate a reaction mechanism involving two trans-PC6 molecules
    1-苯基环己烯 (PC6) 的低温照射产生两个单线态 2 + 2 光二聚体和两个 4 + 2 环加合物。4 + 2 加合物在室温下在低强度灯照射下未观察到,但当 PC6 溶液受到更高强度的激光照射时会大量产生。结果表明涉及两个反式PC6分子的反应机制。这些发现与早期的动力学观察一致,即反式 PC6 的衰变在较低温度下采用显着的二阶成分。瞬态-瞬态反应也发生在三重敏化低温/低强度或室温/高强度辐照条件下。三重敏化辐射还产生大量的 2 + 2 光二聚体,这是由 PC6 三重态对其基态的攻击产生的。量子产率研究表明,3PC6* 添加到其基态的速率在 0.28 到 4.0 × 105 L mol-1 s-1 的范围内,与 t...
  • Photochemistry of cis-1-phenylcyclohexene. Proof of involvement of trans isomer in reaction processes
    作者:W. G. Dauben、H. C. H. A. Van Riel、J. D. Robbins、G. J. Wagner
    DOI:10.1021/ja00515a036
    日期:1979.10
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同类化合物

3,4-双(4-羟基苯基)环丁烷-1,2-二羧酸 3,4-二苯基环丁烷-1,2-二羧酸 1-[2,3-二甲基-4-(2,4,5-三甲氧基苯基)环丁基]-2,4,5-三甲氧基苯 (2,3,4-三苯基环丁基)苯 DL-(1R,2R,3S,4S)-3,4-bis(4-methoxyphenyl)cyclobutane-1,2-dicarboxylic acid tetrakis-1,2,3,4-(4’- carboxyphenyl)cyclobutane 3,3'-dinitro-β-truxinic acid diphenyl 3,4-diphenylcyclobutane-1,2-dicarboxylate DL-(1R,2R,3S,4S)-diphenyl 3,4-diphenylcyclobutane-1,2-dicarboxylate 3,4-bis(2-hydroxy-5-methylphenyl)cyclobutane-1,2-dicarboxylic acid N-(n-pentyl)-3β,4β-bis(3',4'-dimethoxyphenyl)-1α,2α-cyclobutanedicarboximide trans-1,2-diphenylbicyclo[3.1.0.02,4]hexane 8β,8'α-dimethyl-7α,7'β-bis(3-methoxy-4-hydroxyphenyl)cyclobutane 4,4'-((1R,2R,3S,4S)-3,4-dimethylcyclobutane-1,2-diyl)bis(methoxybenzene) caracasandiamide 3β,4β-bis(3',4'-dimethoxyphenyl)-1α-carboxy-2α-<butyl>cylobutanecarboxamide quinic acid diester of 3,4,3',4'-tetrahydroxy-β-truxinic acid 3,3′-difluoro-β-truxinic acid endiandrin B 3,3-Dimethyl-2,4-diphenyl-tricyclo[3.2.0.02,4]heptane (1R,6S,7S,8R)-7,8-Diphenyl-bicyclo[4.2.0]octane 1,5-Diphenyl-quadricyclan dimethyl t-3,t-4-di-(3,4,5-trimethoxyphenyl)cyclobutane-r-1,c-2-dicarboxylate (±)-(1R,5S,6R,7S)-6,7-bis(4-methoxyphenyl)-3-oxabicyclo[3.2.0]heptane 2-((1R,2S,3R,4R)-2-methyl-2-nitro-3,4-diphenylcyclobutyl)acetaldehyde 1α,2α-Di-(2-methoxy-phenyl)-cyclobutan-dicarbonsaeure-(3β,4β)-dimethylester o,o'-Dimethyl-β-truxillsaeuredimethylester 1,2-diisobutyryl-3,4-diphenyl-cyclobutane 3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid (17S,18R,19S,20R)-18,19-bis(3,4-dimethylphenyl)-15,22-diazahexacyclo[21.2.2.211,14.12,6.017,20.010,30]triaconta-1(25),2,4,6(30),7,9,11(29),12,14(28),23,26-undecaene-16,21-dione 3,3-Dimethyl-2,4-diphenyl-endo-tricyclo<3.3.0.02,4>oct-6-en ((1S,2R,3S,4R)-3-Hydroxymethyl-1,4-diphenyl-bicyclo[2.2.0]hex-2-yl)-methanol (1R,7S,8R,11S)-8,11-Diphenyl-3,5-dioxa-4-thia-tricyclo[5.4.0.08,11]undecane 4,4-dioxide 4a,4b-Bis(4-methoxyphenyl)decahydrobiphenylene-1,8-dione 4a,4b-Bis(4-nitrophenyl)decahydrobiphenylene-1,8-dione 8-Methyl-4,4a-diphenyltetrahydro-1h,5h-3,4,4b-(methanetriyl)cyclopenta[1,3]cyclopropa[1,2-b]pyridin-2(3h)-one (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(4-tert-butyl-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester (S,S,S,S)-3,4-bis(2-diphenylphosphinylphenyl)-1,2-cyclobutanedimethyl di(diphenylphosphine) (1R,2R,3R,4R)-3,4-Bis-[2-(diphenyl-phosphinoyl)-phenyl]-cyclobutane-1,2-dicarboxylic acid diethyl ester (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(3,5-dimethyl-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester 4,4'-(3,4-diphenyl-cyclobutane-1,2-diyl)-bis-benzo[h]quinoline 4,4'-(3,4-diphenyl-cyclobutane-1,2-diyl)-bis-benzo[h]quinoline 3,4-diphenyl-3,4-dichlorocyclobutanodicarbox-1,2-dianilide (1S,5R,6R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(4-methoxy-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester 1,2-Diphenyl-1,2,2a,10b-tetrahydro-cyclobuta[l]phenanthrene all-cis-1,2-Dibenzyl-3,4-diphenylcyclobutan (3,4-diphenylcyclobutane-1,2-diyl)bis(phenylmethanone) 1,2-dibenzoyl-3,4-diphenyl-cyclobutane