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2-Ethyl-1,2-dihydro-isochinolin | 37039-54-6

中文名称
——
中文别名
——
英文名称
2-Ethyl-1,2-dihydro-isochinolin
英文别名
2-ethyl-1,2-dihydro-isoquinoline;2-ethyl-1H-isoquinoline
2-Ethyl-1,2-dihydro-isochinolin化学式
CAS
37039-54-6
化学式
C11H13N
mdl
——
分子量
159.231
InChiKey
LDKOKMMYTFCGMT-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

  • 沸点:
    134 °C(Press: 12 Torr)
  • 密度:
    1.006±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    2-Ethyl-1,2-dihydro-isochinolinC,N-Diphenylnitrilimine三乙胺 作用下, 以 为溶剂, 反应 5.0h, 以66%的产率得到(3aS,4S,9bS)-4-Ethyl-1,3-diphenyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline
    参考文献:
    名称:
    Stereochimie de la cycloadditton des diarylnitrilimines sur les n-alkyl et les dialkyl-1,2 dihydro-1,2 isoquinoleines
    摘要:
    DOI:
    10.1016/s0040-4020(01)91394-8
  • 作为产物:
    描述:
    异喹啉 在 lithium aluminium tetrahydride 作用下, 生成 2-Ethyl-1,2-dihydro-isochinolin
    参考文献:
    名称:
    Stereochimie de la cycloadditton des diarylnitrilimines sur les n-alkyl et les dialkyl-1,2 dihydro-1,2 isoquinoleines
    摘要:
    DOI:
    10.1016/s0040-4020(01)91394-8
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文献信息

  • [EN] IONIC LIQUIDS BASED ON OXALIC ACID MONO ESTERS<br/>[FR] LIQUIDES IONIQUES À BASE DE MONOESTERS DE L'ACIDE OXALIQUE
    申请人:BASF SE
    公开号:WO2014056844A1
    公开(公告)日:2014-04-17
    Monosubstituted oxalic acid derivatives of the general formula (I) [A]+[O-C(O)-C(O)-O-X]-, wherein the meaning is: for [A]+, a cation made from an organic moiety A having a formally positively charged heteroatom selected from the group consisting of nitrogen, phosphorus and sulfur, X is a C1 to C30 organic residue, and wherein the following compounds (I) are disclaimed:tetramethylammonium monomethyloxalate methyltri(alkyl)ammonium monomethyloxalate trimethyl(1-hydroxyethyl)ammonium monomethyloxalate methyltriethylammonium monomethyloxalate tetraethylammonium monomethyloxalate n-propyltriethylammonium mono-n-propyloxalate n-butyltriethylammonium mono-n-butyloxalate benzyltriethylammonium monobenzyloxalate cyclohexyldimethylammonium monomethyloxalate dimethyl-phenylammonium monomethyloxalate. Tetrabutylammonium monomethyloxalate N-methylpyridinium monomethyloxalate N-ethylpyridinium monoethyloxalate N-n-propylpyridinium mono-n-propyloxalate N-n-butylpyridinium mono-n-butyl-oxalate N-benzylpyridinium monobenzyloxalate N-methyl-isochinolinium monomethyloxalate N-ethyl-isochinolinium monoethyloxalate N-n-propyl-isochinoliniummono-n-propyloxalate N-n-butyl-isochinolinium mono-n-butyloxalate N-benzyl-isochinolinium monobenzyloxalate.
    单取代草酸衍生物的一般式(I) [A]+[O-C(O)-C(O)-O-X]-,其中含义为:对于[A]+,是由有机基团A形成的阳离子,其正式带正电的杂原子选自氮、磷和硫组成的群,X是一个C1到C30的有机残基,且以下化合物(I)被否认:四甲基铵单甲氧草酸酯 甲基三(烷基)铵单甲氧草酸酯 三甲基(1-羟乙基)铵单甲氧草酸酯 甲基三乙基铵单甲氧草酸酯 四乙基铵单甲氧草酸酯 正丙基三乙基铵单正丙氧草酸酯 正丁基三乙基铵单正丁氧草酸酯 苄基三乙基铵单苄氧草酸酯 环己基二甲基铵单甲氧草酸酯 二甲基苯基铵单甲氧草酸酯。 四丁基铵单甲氧草酸酯 N-甲基吡啶铵单甲氧草酸酯 N-乙基吡啶铵单乙氧草酸酯 N-正丙基吡啶铵单正丙氧草酸酯 N-正丁基吡啶铵单正丁氧草酸酯 N-苄基吡啶铵单苄氧草酸酯 N-甲基异喹啉铵单甲氧草酸酯 N-乙基异喹啉铵单乙氧草酸酯 N-正丙基异喹啉铵单正丙氧草酸酯 N-正丁基异喹啉铵单正丁氧草酸酯 N-苄基异喹啉铵单苄氧草酸酯。
  • ORGANIC ELECTRONIC MATERIAL, POLYMERIZATION INITIATOR AND THERMAL POLYMERIZATION INITIATOR, INK COMPOSITION, ORGANIC THIN FILM AND PRODUCTION METHOD FOR SAME, ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, LIGHTING DEVICE, DISPLAY ELEMENT, AND DISPLAY DEVICE
    申请人:Ishitsuka Kenichi
    公开号:US20130037753A1
    公开(公告)日:2013-02-14
    Disclosed is an organic electronic material comprising charge transporting compounds and ionic compounds having electron-accepting properties and high solubility in a solvent. The organic electronic material is characterized by comprising charge transporting compounds and ionic compounds, and in that at least one of the ionic compounds is any one kind of compounds represented by general formulas (1b)-(3b). (In the formulas Y 1 -Y 6 each independently represent a divalent linking group, R 1 -R 6 each independently represent an electron-attracting organic substituent (these structures can further have substituents and hetero-atoms, and R 1 , R 2 and R 3 , or, R 4 -R 6 can respectively combine and become a ring shape or a polymer shape) and L + represents a monovalent cation.)
    本文揭示了一种有机电子材料,包括具有电荷传输化合物和具有接受电子性质且在溶剂中具有高溶解度的离子化合物。该有机电子材料的特点在于包括电荷传输化合物和离子化合物,并且至少其中一个离子化合物是由通用式(1b)-(3b)表示的化合物中的任意一种。(在式中,Y1-Y6分别表示二价连接基团,R1-R6分别表示吸引电子的有机取代基(这些结构可以进一步具有取代基和杂原子,且R1、R2和R3,或者R4-R6可以分别结合形成环状或聚合物形状),L+表示一价阳离子。)
  • POLARIZED FILM, OPTICAL FILM, AND IMAGE DISPLAY DEVICE
    申请人:NITTO DENKO CORPORATION
    公开号:US20150049380A1
    公开(公告)日:2015-02-19
    A polarizing film, comprising a polarizer; transparent protective films with a water-vapor permeability of 150 g/m2/24 hours or less provided on both sides of the polarizer; and adhesive layers each interposed between the polarizer and one of the transparent protective films, wherein the adhesive layers are formed by applying an active energy ray to an active energy ray-curable adhesive composition containing a radically polymerizable compound, and the transparent protective films are bonded to the polarizer with the adhesive layers.
    一种偏光膜,包括偏光器;透明保护膜,在偏光器的两侧提供,其水汽渗透率为每平方米每24小时150克或以下;以及粘合层,每个粘合层夹在偏光器和一个透明保护膜之间,其中粘合层是通过将活性能量射线应用于含有自由基聚合化合物的活性能量射线可固化粘合剂组成的,透明保护膜与偏光器通过粘合层粘合在一起。
  • SULFONIUM SALT, PHOTOACID GENERATOR, AND PHOTOCURABLE COMPOSITION AND CURED BODY THEREOF
    申请人:Suzuki Issei
    公开号:US20110039205A1
    公开(公告)日:2011-02-17
    An object of the present invention is to provide a sulfonium salt that has sufficient photosensitivity by active energy rays, such as visible light, ultraviolet rays, electron beams, and X-rays. The present invention is a sulfonium salt represented by formula (1). It is noted that R 1 is a group represented by formula (2); R 2 and R 3 each represent an aryl group having 6 to 30 carbon atoms, a heterocyclic hydrocarbon group having 4 to 30 carbon atoms, an alkyl group having 1 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, or an alkynyl group having 2 to 30 carbon atoms; X − represents a monovalent polyatomic anion; R 4 to R 6 each represent an alkyl group, or the like; k represents an integer of 0 to 4; m represents an integer of 0 to 3; n represents an integer of 0 to 4; and A represents a group represented by —S—, —O—, —SO—, —SO 2 —, or —CO—.
    本发明的目的是提供一种具有足够光敏度的烷基硫鎓盐,能够通过活性能量射线,如可见光、紫外线、电子束和X射线来激发。本发明是一种由式(1)表示的烷基硫鎓盐。其中,R1是由式(2)表示的基团;R2和R3分别表示具有6至30个碳原子的芳基基团、具有4至30个碳原子的杂环烃基团、具有1至30个碳原子的烷基基团、具有2至30个碳原子的烯基基团或具有2至30个碳原子的炔基基团;X-表示单价多原子阴离子;R4至R6分别表示烷基基团或类似物;k表示0至4的整数;m表示0至3的整数;n表示0至4的整数;A表示由—S—、—O—、—SO—、—SO2—或—CO—表示的基团。
  • indenoisoquinolines as topoisomerase inhibitors I useful as antineoplastic agents
    申请人:Purdue Research Foundation
    公开号:EP2050452A1
    公开(公告)日:2009-04-22
    A number of indenoisoquinolines were prepared and evaluated for cytotoxicity in human cancer cell cultures and for activity vs. topoisomerase I. The two most cytotoxic indenoisoquinolines proved to be cis-6-ethyl-5,6,12,13-tetrahydro-2,3-dimethoxy-8,9-(methylenedioxy)-5,11-dioxo-11H-indeno[1,2-c]isoquinoline and cis-6-allyl-5,6,12,13-tetrahydro-2,3-dimethoxy-8,9-(methylenedioxy)-5,11-dioxo-(11H)indeno[1,2-c]isoquinoline. Two of the most potent topoisomerase I inhibitors were 6-(3-carboxy-1-propyl)-5,6-dihydro-5,11-dioxo-11H-indeno[1,2-c]isoquinoline (26) and 6-ethyl-2,3-dimethoxy-8,9-(methylenedioxy)11H-indeno[1,2-c]isoquinolinium chloride (27). Two additional potent topoisomerase I inhibitors, 6-allyl-5,6-dihydro-2,3-dimethoxy-8,9-(methylenedioxy)-5,11-dioxo-11H-indeno[1,2-c]isoquinoline (13c) and 5,6-dihydro-6-(4-hydroxybut-1-yl)-2,3-dimethoxy-8,9-methylenedioxy-5,11-dioxo-(11H)indeno[1,2-c]isoquinoline (19a), did not unwind DNA and did not affect topoisomerase II.
    研究人员制备了多种茚并异喹啉,并对其在人类癌细胞培养物中的细胞毒性以及对拓扑异构酶 I 的活性进行了评估。结果表明,两种细胞毒性最强的茚异喹啉分别是顺式-6-乙基-5,6,12,13-四氢-2,3-二甲氧基-8,9-(亚甲基二氧基)-5,11-二氧代-11H-茚并[1、2-c]异喹啉和顺式-6-烯丙基-5,6,12,13-四氢-2,3-二甲氧基-8,9-(亚甲基二氧基)-5,11-二氧代-11H-茚并[1,2-c]异喹啉。两种最有效的拓扑异构酶 I 抑制剂是 6-(3-羧基-1-丙基)-5,6-二氢-5,11-二氧代-11H-茚并[1,2-c]异喹啉(26)和 6-乙基-2,3-二甲氧基-8,9-(亚甲二氧基)11H-茚并[1,2-c]异喹啉氯化铵(27)。另外两种强效拓扑异构酶 I 抑制剂是 6-烯丙基-5,6-二氢-2,3-二甲氧基-8,9-(亚甲基二氧基)-5,11-二氧代-11H-茚并[1,2-c]异喹啉(13c)和 5、6-(4-羟基丁-1-基)-2,3-二甲氧基-8,9-亚甲基二氧基-5,11-二氧代-11H-茚并[1,2-c]异喹啉(19a)不会解开 DNA,也不会影响拓扑异构酶 II。
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