摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,9-diphenyl-1,8-nonadiyne-3,7-dione | 303142-47-4

中文名称
——
中文别名
——
英文名称
1,9-diphenyl-1,8-nonadiyne-3,7-dione
英文别名
1,9-Diphenylnona-1,8-diyne-3,7-dione;1,9-diphenylnona-1,8-diyne-3,7-dione
1,9-diphenyl-1,8-nonadiyne-3,7-dione化学式
CAS
303142-47-4
化学式
C21H16O2
mdl
——
分子量
300.357
InChiKey
VZUIDTUHTAZGKD-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):
    4.4
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 下游产品
    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:
    参考文献:
    名称:
    Synthesis and Protein Degradation Capacity of Photoactivated Enediynes
    摘要:
    The viability of proteins as targets of thermally and photoactivated enediynes has been confirmed at the molecular level. Model studies using a labeled substrate confirmed the efficacy of atom transfer from diyl radicals produced from enediynes to form captodatively stabilized carbon centered aminoacyl radicals, which then undergo either fragmentation or dimerization. To exploit this finding, a family of enediynes was developed using an intramolecular coupling strategy. Derivatives were prepared and used to target specific proteins, showing good correlation between affinity and photoinduced protein degrading activity. The findings have potential applications in the design of artificial chemical proteases and add to our understanding of the mechanism of action of the clinically important enediyne antitumor antibiotics.
    DOI:
    10.1021/jo051403q
  • 作为产物:
    描述:
    戊二酰基二氯正丁基锂三乙胺 作用下, 以 四氢呋喃正己烷二氯甲烷 为溶剂, 反应 2.0h, 生成 1,9-diphenyl-1,8-nonadiyne-3,7-dione
    参考文献:
    名称:
    Synthesis and Protein Degradation Capacity of Photoactivated Enediynes
    摘要:
    The viability of proteins as targets of thermally and photoactivated enediynes has been confirmed at the molecular level. Model studies using a labeled substrate confirmed the efficacy of atom transfer from diyl radicals produced from enediynes to form captodatively stabilized carbon centered aminoacyl radicals, which then undergo either fragmentation or dimerization. To exploit this finding, a family of enediynes was developed using an intramolecular coupling strategy. Derivatives were prepared and used to target specific proteins, showing good correlation between affinity and photoinduced protein degrading activity. The findings have potential applications in the design of artificial chemical proteases and add to our understanding of the mechanism of action of the clinically important enediyne antitumor antibiotics.
    DOI:
    10.1021/jo051403q
点击查看最新优质反应信息

文献信息

  • The Photo-Dehydro-Diels-Alder (PDDA) Reaction - A Powerful Method for the Preparation of Biaryls
    作者:Pablo Wessig、Gunnar Müller、Charlotte Pick、Annika Matthes
    DOI:10.1055/s-2006-958949
    日期:2007.2
    The photochemically initiated dehydro-Diels-Alder (PDDA) reaction is an efficient and versatile method for the prepa- ration of biaryls. The ring closure may take place both inter- and in- tramolecularly, of which the intramolecular variant is more productive from the preparative point of view. A variety of linkers can be employed to connect the ynone moiety, which acts as the chromophore, with another
    光化学引发的脱氢-狄尔斯-阿尔德 (PDDA) 反应是制备联芳基化合物的一种有效且通用的方法。闭环可以发生在分子间和分子内,从制备的角度来看,分子内变体的生产效率更高。可以使用多种接头将充当发色团的ynone部分与另一个乙炔基团连接起来,从而实现大的结构多功能性。此处还将讨论影响 PDDA 反应位点选择性的原理。
  • Synthesis of carbonyl and dicarbonyl compounds from organometallic reagents and N-imidazolium-N-methyl amides and bis-amides
    作者:María A. de las Heras、Juan J. Vaquero、JoséL. García Navio、Julio Alvarez-Builla
    DOI:10.1016/0040-4020(96)00882-4
    日期:1996.11
    A new method for the synthesis of selective acylating agents is described from the reaction of carboxylic acids with 3-methyl-1-methylamino-3H-imidazol-1-ium salts in the presence of appropriate coupling reagents. The amides and bis-amides thus prepared reacted selectively with organometallics to afford ketones and diketones and with DIBALH to give aldehydes and dialdehydes in high yields.
    在适当的偶联剂存在下,由羧酸与3-甲基-1-甲基氨基-3 H-咪唑-1-鎓盐的反应描述了一种合成选择性酰化剂的新方法。如此制备的酰胺和双酰胺与有机金属选择性反应,得到酮和二酮,与DIBALH反应以高产率得到醛和二醛。
  • Dental Restorative Materials Based on Polymerizable Azides and Alkynes
    申请人:Ivoclar Vivadent AG
    公开号:US20150164750A1
    公开(公告)日:2015-06-18
    The invention relates to a dental restorative material on the basis of at least one compound of one of the Formulae The invention also relates to the use of the dental restorative materials according to the invention for preparing dental composites, preferably composite blanks, which are suitable in particular for mechanical processing by means of computer-aided processing techniques such as milling and grinding processes, and which are suitable above all for preparing dental restoration materials such as inlays, onlays, crowns, bridges or veneering materials.
    本发明涉及一种牙科修复材料,其基础是至少一种符合以下式之一的化合物。本发明还涉及根据本发明的牙科修复材料用于制备牙科复合材料,优选是适用于通过计算机辅助加工技术(如铣削和研磨过程)进行机械加工的复合坯料,特别适用于制备牙科修复材料,如嵌体、套体、冠、桥梁或贴面材料。
  • The Photo-Dehydro-Diels-Alder Reaction: An Efficient Route to Naphthalenes
    作者:Pablo Wessig、Gunnar Müller、Andreas Kühn、Robert Herre、Haiko Blumenthal、Stefanie Troelenberg
    DOI:10.1055/s-2005-865316
    日期:——
    photochemical route to naphthalenes is presented. The [4+2] cycloaddition takes place between 3-arylynones and arylacetylenes, in which these moieties may be located intwo molecules (intermolecular PDDA, 1) or in the same molecule (intramolecular PDDA, 5 and 9). Especially the latter approach is attractive from a preparative point of view and permits a straightforward access to highly functionalized naphthalenes
    提出了一种新的光化学合成萘的途径——光脱氢狄尔斯阿尔德反应(PDDA)。[4+2] 环加成发生在 3-芳基酮和芳基乙炔之间,其中这些部分可能位于两个分子(分子间 PDDA,1)或同一分子(分子内 PDDA,5 和 9)中。特别是后一种方法从制备的角度来看是有吸引力的,并且允许直接获得高度官能化的萘。与对称反应物5相比,不对称反应物9的辐照提供了两种异构萘。我们发现区域选择性很容易受到芳环中适当定位的取代基和封闭不需要的位置的影响。值得注意的是,PDDA 可用于制备联萘,如 14 和 16 的形成所示。
  • Dentalwerkstoffe auf Basis von polymerisierbaren Aziden und Alkinen
    申请人:Ivoclar Vivadent AG
    公开号:EP2883528A1
    公开(公告)日:2015-06-17
    Die Erfindung betrifft einen Dentalwerkstoff auf Basis mindestens einer Verbindung mit einer der Formeln Die Erfindung betrifft auch die Verwendung der erfindungsgemässen Dentalwerkstoffe zur Herstellung von dentalen Kompositen, vorzugsweise Komposit-Formkörpern, die insbesondere für die maschinelle Bearbeitung mittels computergestützter Verarbeitungstechniken wie Fräs- und Schleifverfahren geeignet sind und sich vor allem zur Herstellung von dentalen Restaurationsmaterialien wie Inlays, Onlays, Kronen, Brücken oder Verblendmaterialien eignen.
    本发明涉及一种牙科材料,其基础是至少一种具有以下式子之一的化合物 本发明还涉及根据本发明的牙科材料用于生产牙科复合材料,最好是复合材料模制件,这种模制件特别适合通过计算机辅助加工技术(如铣削和研磨工艺)进行加工,特别适合生产牙科修复材料,如嵌体、镶嵌体、牙冠、牙桥或贴面材料。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐