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9,10-dihydro-9,10-ethanoanthracene-11,12-dicarbohydrazide | 38253-49-5

中文名称
——
中文别名
——
英文名称
9,10-dihydro-9,10-ethanoanthracene-11,12-dicarbohydrazide
英文别名
9,10-Dihydro-9,10-ethanoanthracene-11,12-dicarboxylic dihydrazide;tetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaene-15,16-dicarbohydrazide
9,10-dihydro-9,10-ethanoanthracene-11,12-dicarbohydrazide化学式
CAS
38253-49-5
化学式
C18H18N4O2
mdl
——
分子量
322.367
InChiKey
VSIXZNXJYWMUMM-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    110
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    9,10-dihydro-9,10-ethanoanthracene-11,12-dicarbohydrazide乙醇 为溶剂, 反应 9.0h, 生成
    参考文献:
    名称:
    新型多齿缩氨基硫脲的 Zn(II)、Cd(II) 和 Hg(II) 配合物的合成、表征、DFT 分子建模和生物学研究
    摘要:
    摘要 新型配体 2,2'-(9,10-dihydro-9,10-ethanoanthracene-11,12-dicarbonyl)bis(N-ethyl hydrazine-1-carbothioamide) (H6ETS) 及其与 Zn(II )、Cd(II) 和 Hg(II) 是使用物理化学技术合成和表征的。配体的 IR 和 1H-NMR 光谱数据表明它以两种形式存在,酮硫酮和烯醇硫酮。金属配合物光谱数据显示,在 Zn(II) 配合物中,配体作为双负六齿,而在 Hg(II) 配合物中,它以双负四齿方式反应。此外,配体通过羰基和 N2H 基团以中性双齿方式与 Cd(II) 离子螯合。Cd(II) 配合物的热重分析证实配位球外部或内部不存在水分子。此外,使用 Coats-Redfern 和 Horowitz-Metzger 方法评估热力学参数。配体及其 Cd (II) 配合物的键长和角度
    DOI:
    10.1016/j.molstruc.2018.12.064
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文献信息

  • Novel VO (IV) complexes derived from a macrochelates: Synthesis, characterization, molecular modeling and<i>in vivo</i>insulin‐mimic activity studies
    作者:Ola A. El‐Gammal、M. Gaber、Sh. A. Mandour
    DOI:10.1002/aoc.5699
    日期:2020.9
    into a potential medicinal application of vanadium coordination compounds for the oral treatment of diabetes, new mono and bimetallic VO (IV) complexes with N,N′‐(2,2′‐(9,10‐dihydro‐9,10‐ethanoanthracene‐11,12‐dicarbonyl) bis (hydrazine‐1‐carbonothioyl)) dibenzamide (H6EBT) and 2,2′‐((9S,10S,11R,12R)‐9,10‐dihydro‐9,10‐ethanoanthracene‐11, 12‐dicarbonyl) bis (N‐phenylhydrazine‐1‐carboxamide) (H6EPH) have
    为了广泛研究钒配位化合物在糖尿病的口服治疗中的潜在医学应用,新的单和双金属VO(IV)配合物与N,N'-(2,2'-(9,10-dihydro- 9,10-乙基蒽-11,12-二羰基)双(肼-1-碳硫基)二苯甲酰胺(H 6 EBT)和2,2'-((9S,10S,11R,12R)-9,10-二氢分离并鉴定了9,10-乙基蒽-11,12-二羰基)双(N-苯基肼-1-羧酰胺)(H 6 EPH)。FTIR和NMR光谱数据表明,H 6 EBT充当中性三齿和二元六齿,而H 6EPH为二元三齿和四元六齿。电子和ESR光谱表明配合物具有八面体几何形状。[(VO)(H的ESR谱6 EBT)(SO 4)]。5H 2 O的表达式良好分辨的超精细八线图案典型的单核络合物氧钒与G G光谱⊥ = 1.9这表明该配体的供电子原子ONS与形成八面体几何形状的两个螯合环共面。另外,高平行超精细分裂值,A = 0.0108,比一个垂直(A
  • Synthesis, characterization, biological activity of binuclear Co(II), Cu(II) and mononuclear Ni(II) complexes of bulky multi-dentate thiosemicarbazide
    作者:O.A. El-Gammal、I.M. Abd Al-Gader、A.A. El-Asmy
    DOI:10.1016/j.saa.2014.01.119
    日期:2014.7
    ground state. Also, the thermal behavior and kinetic parameters were determined. Furthermore, the title compounds were investigated for their antibacterial activity using inhibition zone diameter and for DNA degradation, superoxide-scavenging activity as well as hydroxyl radicals that generated by the oxidation of cytochrome c in L-ascorbic acid/CuSO4-cytochrome c system.
    9,10-二氢-9,10-乙基蒽-11,12-二羰基)双(N-乙基肼-1-碳硫酰胺)(H6ETS)(1)对Co(2 +),Ni(2+)的螯合行为和Cu(2+)已被研究。光谱数据表明,配体充当双负和/或单负多齿。分离的Ni(II)和Cu(II)络合物为方形,而Co(II)为四面体。Cu(II)配合物的EPR谱证实模拟轴向自哈密顿体,显示出四线模式,具有源自亚胺氢氮原子的氮超超细偶合,并具有大量四面体形变,导致拟方平面几何具有不成对电子的电子具有d(x(2)-y(2))基态。此外,确定了热行为和动力学参数。此外,
  • Synthesis and characterization of novel dicarbohydrazide derivatives with electrochemical and theoretical approaches as potential corrosion inhibitors for N80 steel in a 3.5% NaCl solution
    作者:Y. M. Abdallah、Ola. A. El-Gammal、Hany M. Abd El-Lateef、K. Shalabi
    DOI:10.1039/d2ra01751b
    日期:——

    Two novel dicarbohydrazide derivatives (H2HEH) and (H2MEH) were synthesized and tested as corrosion inhibitors for N80 steel in 3.5% NaCl solutionviaelectrochemical and theoretical approaches.

    两种新的二氨基甲酰肼衍生物(H2HEH)和(H2MEH)被合成,并通过电化学和理论方法测试其作为3.5% NaCl溶液中N80钢的缓蚀剂。
  • Waterborne adhesive formulations
    申请人:Akzo Nobel Coatings International B.V.
    公开号:EP2246403A1
    公开(公告)日:2010-11-03
    This application relates to floor or contact adhesives which are provided as a water-borne formulation comprising: a cross-linkable binder resin having a glass transition temperature (Tg) of less than +10°C; Optionally, a crosslinking agent;, and, optionally a tackifier and / or a plasticiser; wherein the volatile organic compound (VOC) level of said formulation is less than 0.5% by weight. The cross-linkable binder resin should preferably have a glass transition temperature (Tg) in the range from +10°C to -90°C and furthermore should preferably comprise a carbonyl functional (meth)acrylate or vinyl copolymer prepared from a monomer mixture comprising alkyl (meth)acrylate ester monomers and / or vinyl monomers, and diacetonacrylamide (DAAM) monomers. The preferred utility of the water-borne formulation is as a floor or flooring adhesive.
    本申请涉及以水性配方形式提供的地板胶或接触胶,其中包括:玻璃化转变温度(Tg)小于 +10°C 的可交联粘合剂树脂;可选的交联剂;以及可选的增粘剂和/或增塑剂;其中所述配方的挥发性有机化合物(VOC)含量按重量计小于 0.5%。可交联粘合剂树脂的玻璃化转变温度(Tg)最好在 +10°C 至 -90°C 之间,此外,最好包含由烷基(甲基)丙烯酸酯单体和/或乙烯基单体以及二丙酮丙烯酰胺(DAAM)单体组成的单体混合物制备的羰基官能团(甲基)丙烯酸酯或乙烯基共聚物。水性配方的首选用途是地板或地坪粘合剂。
  • One part, fast-setting, aqueous adhesive emulsions
    申请人:3M INNOVATIVE PROPERTIES COMPANY
    公开号:US10221343B2
    公开(公告)日:2019-03-05
    The present disclosure relates to acrylic adhesive emulsions comprising a core-shell polymeric component comprising an inner core and an outer shell containing at least one pendent functional group; a polyfunctional component capable of reacting with at least one of the pendent functional groups on the outer shell; wherein the inner core is free of functional groups reactive with the pendent functional groups on the outer shell; and wherein the pH of the emulsion is 6.5 or less; and wherein the emulsion is a fast-setting, one part, aqueous, adhesive. Bonded articles made therefrom, and methods of bonding articles using these emulsions are also disclosed.
    本公开涉及丙烯酸粘合剂乳液,该乳液包含核壳聚合物成分,该聚合物成分包括内核和外壳,外壳含有至少一个悬垂官能团;能够与外壳上的至少一个悬垂官能团反应的多功能成分;其中内核不含与外壳上的悬垂官能团反应的官能团;乳液的 pH 值为 6.5 或更低;乳液是一种快速固化的单组分水性粘合剂。此外,还公开了由其制成的粘合制品以及使用这些乳液粘合制品的方法。
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同类化合物

鬼臼酸哌啶基腙氮氧自由基 鬼臼酸 鬼臼毒醇 苦鬼臼毒醇 米托肼 甘尔布林 珠子草次素 消泡剂 愈创木素 异落叶松脂素 异紫杉脂素9,9'-缩丙酮 异紫杉脂素 大侧柏酸 四环[6.6.2.02,7.09,14]十六烷-2(7),3,5,9(14),10,12-己烯-15,15,16,16-四甲腈 叶下珠新素 五脂素A1 7,8,9,9-四去氢异落叶松树脂醇 7,14-二氢-7,14-乙桥二苯并[a,h]蒽-15,16-二羧酸二钠盐 7,14-二氢-7,14-乙桥二苯并[a,h]蒽-15,16-二甲酸 6,8-二溴-4-氧代-4H-1-苯并吡喃-3-甲醛 5a-苯基-5a,14c-二氢苯并[a]茚并[2,1-c]芴-5,10-二酮 1-苯基-1,2,3,4-四氢-萘-2,3-二羧酸 1-(3,4-二羟基苯基)-6,7-二羟基-1,2-二氢萘-2,3-二甲酸 1-(3,4-二甲氧基苯基)-1,2,3,4-四氢-6,7-二甲氧基-2,3-萘二甲醇 1-(3,4-二甲氧基-苯基)-6,7-二甲氧基-1,2,3,4-四氢-萘-2,3-二羧酸 (7S,8S,9R)-9-(3,4-二甲氧基苯基)-6,7,8,9-四氢-4-甲氧基-7,8-双(甲氧基甲基)萘并[1,2-D]-1,3-二恶茂 (7S,8R,9R)-9-(1,3-苯并二氧戊环-5-基)-7,8-二甲基-6,7,8,9-四氢苯并[g][1,3]苯并二氧戊环 (1S,2R,3S)-1-(3,4-二甲氧基苯基)-1,2,3,4-四氢-6,7-二甲氧基-2,3-二甲基-萘 (11S,12R)-9,10-乙桥-9,10-二氢蒽-11,12-二甲酸 (-)-南烛木树脂酚 (+)-异落叶松脂素 (1RS,2SR)-1,2-dihydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxynaphthalene-2,3-dicarboxylic acid dimethyl ester (+/-)-(1R,2S,3R)-12-benzyl-4-hydroxy-6,7-methylenedioxy-1-phenyl-2,3,4-trihydrobenzo[f]isoindol-13-one (+/-)-dimethoxy-epi-isopicropodophyllin N-benzyl lactam (+/-)-(1R,2R,3S)-12-benzyl-6,7-methylenedioxy-4-oxo-1-phenyl-2,3-dihydrobenzo[f]isoindol-13-one (+)-ovafolinin B (5R,6R)-methyl 7-(6-fluoro-1H-benzo[d]imidazol-2-yl)-5-(3,4,5-trimethoxyphenyl)-5,6-dihydronaphtho[2,3-d][1,3]dioxole-6-carboxylate 2,5,8-trimethoxy-4a,9,9a,10-tetrahydro-9,10-[1,2]benzenoanthracene-1,4-dione 2,11-dichloro-13b-phenylbenzo[a]indeno[1,2-c]fluorene-9,14(8bH,13bH)-dione rel-(1R,4aR,9S,9aS,10R)-4a,9,9a,10-tetrahydro-9,10-diphenylspiro[9,10-epoxyanthracene-1(4H),2'-oxiran]-4-one 1,4-diphenyl-1,2,3,4-tetrahydro-1,4-epoxido-naphthalene-2,3-dicarboxylic acid diethyl ester rel-(1R,4aS,9R,9aS,10S)-4a,9,9a,10-tetrahydro-9,10-diphenylspiro[9,10-epoxyanthracene-1(4H),2'-oxetane]-4-one endo-2,5-diphenyl-3,4-benzo-14-oxatetracyclo<7.2.2.12,5.01,6>tetradec-3-ene 1a,2,7,7a-tetrahydro-2,7-epoxy-1a-methyl-1,2,7-triphenylbenzonaphthothiophenium triflate endo-2,5-diphenyl-3,4-benzo-14-oxatetracyclo<6.3.2.12,5.01,6>tetradec-3-ene (1S,8R,9S,10S)-1,8-diphenyl-10-methyl-11-oxa-tricyclo[6.2.1.02,7]undeca-2(7),3,5-triene-9-carboxaldegyde 13b-phenylbenzo[a]indeno[1,2-c]fluorene-9,14(8bH,13bH)-dione (1R,2R)-7-methyl-1,2,3-tris(4-methylphenyl)-1,2-dihydronaphthalene methyl 9-deoxy-9-oxo-α-apopicropodophyllate 9-n-hexylimine (15R)-13-(4-fluorophenyl)-10-hydroxy-10,11-dihydro-9H-9,10-[3,4]epipyrroloanthracene-12,14(13H,15H)-dione