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2,3-dihydro-2,2-dimethyl-1H-phenalene-1,3-dione | 20494-84-2

中文名称
——
中文别名
——
英文名称
2,3-dihydro-2,2-dimethyl-1H-phenalene-1,3-dione
英文别名
2,2-dimethyl-2,3-dihydrophenalene-1,3-dione;2,3-dihydro-2,2-dimethylphenalene-1,3-dione;2,2-dimethyl-1H-phenalene-1,3(2H)-dione;2,2-dimethyl-phenalene-1,3-dione;2,2-Dimethyl-phenalen-1,3-dion;2.2-Dimethyl-perinaphthindandion-(1.3);2,2-Dimethylphenalene-1,3-dione
2,3-dihydro-2,2-dimethyl-1H-phenalene-1,3-dione化学式
CAS
20494-84-2
化学式
C15H12O2
mdl
——
分子量
224.259
InChiKey
AYWMGPVWKRJKOT-UHFFFAOYSA-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:
    83-84 °C
  • 沸点:
    385.2±22.0 °C(Predicted)
  • 密度:
    1.218±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Potential Protein Kinase C Inhibitors. 8,9,10,11α:-Tetrahydro-7αH-7,11-methano-12,12-dimethylcycloocta[de]naphthyl-9-amines
    作者:Martin P Wilson、Ralph E Bowman、H John Smith、Paul J Nicholls、Michael J E Hewlins
    DOI:10.1111/j.2042-7158.1996.tb07116.x
    日期:2011.4.12
    Abstract

    The synthesis of the 9α- and 9β-epimers of 8, 9, 10, 1 1α-tetrahydro-7αH-7, 11-methano-12, 12-dimethylcycloocta [de] naphthyl-9-amine is described.

    摘要

    本文描述了8, 9, 10, 11α-四氢-7αH-7, 11-甲基-12, 12-二甲基环辛[de]萘基-9-胺的9α和9β-异构体的合成。

  • Conjugated Biradical Intermediates: Spectroscopic, Kinetic, and Trapping Studies of 2,2-Dimethyl-1,3-perinaphthadiyl
    作者:Erich Hasler、Ernst Gassmann、Jakob Wirz
    DOI:10.1002/hlca.19850680328
    日期:1985.5.15
    decay of this reactive intermediate which is persistent at 77 K in the triplet ground state (3a) and rather long-lived (400 μs) at room temperature. When formed in its lowest singlet state (1a), the biradical is too short-lived to undergo intersystem crossing to 3a or bimolecular reactions. Thus, 3a is formed exclusively from the excited triplet state of the precursor compounds, 31* or 33*. The monomolecular
    所述双基-2,2-二甲基-1,3- perinaphthadiyl(一)是从两个不同的前体,所述naphthocyclopropane产生1和偶氮化合物2,并从每个由三个不同的途径(热解,直接光解,和三线态敏化,流程1)。来自闪速光解,低温光谱和产物分析的综合证据提供了这种活性中间体的形成和衰变的详细机理图,该中间体在三重态基态(3 a)下持续存在于77 K且寿命较长(室温下约400μs)。以最低的单重态(1 a),所述双基是过于短暂经历系间窜越到3一个或双分子反应。因此,3一从所述前体化合物的激发三重态,仅仅形成3 1 *或3 3 *。自旋势垒可阻止3 a的单分子衰减;3个一个发起丙烯腈聚合,并通过捕获3 Ò 2。
  • Preparation, X-ray structures and unique redox reactions of novel 2,2′-(2,2-dimethylpropane-1,3-diylidene)bis(1,3-benzodithiole)-type electron donors fused with a naphthalene ring
    作者:Takanori Suzuki、Tsuyoshi Yoshino、Masakazu Ohkita、Takashi Tsuji
    DOI:10.1039/b005078o
    日期:——
    The title π-extended TTF derivatives 1 and 2 were prepared from the corresponding diketones by Wittig–Horner reactions. Donor 1 with a naphthalene-1,8-diyl skeleton adopts a butterfly-shaped geometry; its oxidation caused transannular C–C bonding to give the dicationic cyclopropane derivative 42+2+2+, from which 1 was regenerated upon 2e-reduction. The 2,3-diyl isomer 2 possesses, on the other hand, an almost planar π-system and underwent 2-stage 1e-oxidation, thus allowing the isolation of both 2˙+++ and 22+2+2+ as stable salts.
    标题α-延伸的TTF衍生物1和2是通过Wittig-Horner反应从相应的二酮制备的。具有萘-1,8-二基骨架的给体1采用蝴蝶形几何形状;它的氧化引起跨环C-C键合,得到双阳离子环丙烷衍生物42+2+2+,其中1在2e-还原后再生。另一方面,2,3-二基异构体 2 拥有几乎平面的 α-系统,并经历了 2 阶段 1e-氧化,因此可以分离 2α+++ 和 22+2+2+稳定的盐。
  • Microsystems Technology (MST) and MEMS Applications: An Overview
    作者:Job Elders、Vincent Spiering、Steve Walsh
    DOI:10.1557/mrs2001.69
    日期:2001.4

    Microelectromechanical systems (MEMS), microsystems technology (MST), and micromachines are roughly synonymous terms applied in the United States, Europe, and Japan, respectively, for manufacturing technologies that are enabling miniaturization and the development of useful products.

    微电子机械系统(MEMS),微系统技术(MST)和微机器是在美国,欧洲和日本分别应用的大致同义词,用于启用微型化和有用产品的开发的制造技术。
  • Knorr, Rudolf; Ruhdorfer, Jakob; Mehlstaeubl, Johann, Chemische Berichte, 1993, vol. 126, # 3, p. 747 - 754
    作者:Knorr, Rudolf、Ruhdorfer, Jakob、Mehlstaeubl, Johann、Boehrer, Petra、Stephenson, David S.
    DOI:——
    日期:——
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同类化合物

迫萘合環己-1,3-二酮 赫金青霉素 萘嵌苯酮 富拉烯酮 9-羟基-萘嵌苯-1-酮 9-甲基氨基-萘嵌苯-1-酮 9-巯基-萘嵌苯-1-酮 9-去甲基FR-901235 9-二甲基氨基-1H-萘嵌苯-1-酮 9-丁氧基-1H-萘嵌苯-1-酮 6b,7a-二氢-7H-环丙并[a]苊烯-7-胺盐酸盐(1:1) 6-羟基-3-甲基-1H-萘嵌苯-1-酮 6-羟基-1H-萘嵌苯-1-酮 6-溴-1H-萉 6-氨基-1-萉酮 3-羟基-1H-PHENALEN-1-酮 2-甲氧基非那烯酮 2-甲基-1-氧代-1H-非那烯-3-乙酸 2-氯-6-(3-羟基丙基)氨基-1H-萉-1-酮 2,3-二氢-6-甲氧基萘嵌苯-1-酮 2,3-二氢-1H-萉 2,3-二氢-1H-苯并-1-酮 1H-非那烯并[2,1-d][1,3]噻唑 1H-非那烯 1H-萘嵌苯-1-酮腙 1-硫酮-9-甲基氨基-非那烯 (R)-8,9-二氢-4,5,6,7-四羟基-1,8,8,9-四甲基-3H-非那烯并(1,2-b)呋喃-3-酮 2-hydroxy-2-piperidino-phenalene-1,3-dione 9-[(4-pyrimidin-2-yl)piperazin-1-yl]-1H-phenalen-1-one N-[2-(4,9-dimethoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]butanamide N-[2-(9-methoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]butanamide 9-methyl-9-(2-methylpropenyl)-8,9-dihydrophenaleno[1,2-b]furan-7-one 3-((cyclohexylmethyl)amino)-6-(cyclohexylthio)-1-oxo-1H-phenalene-2-carbonitrile 9-(4-benzylpiperazin-1-yl)-1H-phenalen-1-one perchlorophenalenyl radical 6-((4-bromophenyl)thio)-1-oxo-1H-phenalene-2,3-dicarbonitrile methyl 3-((6-((4-bromophenyl)thio)-2-cyano-1-oxo-1H-phenalen-3-yl)amino)propanoate 3-((6-((4-bromophenyl)thio)-2-cyano-1-oxo-1H-phenalen-3-yl)amino)propanoic acid 3-((6-((4-bromophenyl)thio)-2-cyano-1-oxo-1H-phenalen-3-yl)amino)-N-(2-(2-hydroxyethoxy)ethyl)propanamide 1,1-dimethyl-1a,11b-dihydro-1H-benzo[k]cyclopropa[4,5]cyclopent[1,2,3-cd]fluoranthene 6-(cyclopentylthio)-1-oxo-1H-phenalene-2,3-dicarbonitrile 5-propyl-9-hydroxyphenalenone N-[2-(4,9-dimethoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]propanamide N-[2-(4-methoxy-2,3-dihydro-1H-1-phenalenyl)ethyl]propanamide N-benzyl-1,2,3,10-tetrahydronaphtho[1,8-fg]indol-7-yl trifluoromethanesulfonate N-benzyl-7-ethyl-1,2,3,10-tetrahydronaphtho[1,8-fg]indole 1-oxo-1H-phenalene-2,3-dicarbonitrile 1-((1-oxo-1H-phenalen-2-yl)methyl)pyridinium chloride 9-[(2-hydroxyethyl)(methyl)amino]-1H-phenalen-1-one 6-phenylsulfanyl-2,3-dicyanophenalenone