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1H-thieno[3,4-d]imidazol-2(3H)-one | 75960-44-0

中文名称
——
中文别名
——
英文名称
1H-thieno[3,4-d]imidazol-2(3H)-one
英文别名
1H,3H-thieno[3,4-d]imidazol-2-one;1H,3H-Thieno[3,4-d]imidazol-2-on;1,3-dihydrothieno[3,4-d]imidazol-2-one
1H-thieno[3,4-d]imidazol-2(3H)-one化学式
CAS
75960-44-0
化学式
C5H4N2OS
mdl
——
分子量
140.166
InChiKey
LIKMRBJSBUADIU-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:
    200 °C
  • 沸点:
    122.7±9.0 °C(Predicted)
  • 密度:
    1.451±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.2
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    69.4
  • 氢给体数:
    2
  • 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:
    π-electron conjugated compound, manufacturing method therefor, and π-electron conjugated polymer obtained using same
    摘要:
    提供了一种π-电子共轭聚合物,其具有适用于作为电致变色材料的结构单元,该结构单元由一般式(2)表示,从预期的有色状态变为无色状态,一种作为该聚合物原料的新化合物,以及一种制备该聚合物的方法:其中每个X独立地表示从氧原子、硫原子、—NH—和—NR1—(其中R1是具有1到20个碳原子的可选择取代的烷基基团或具有6到20个碳原子的可选择取代的芳基基团)中选择的一个;每个Y独立地表示氧原子或硫原子;每个Z独立地表示选择自氢原子和具有1到20个碳原子的可选择取代的有机基团的一种;W是选择自乙炔基团、可选择取代的乙烯基团、可选择取代的芳基基团和可选择取代的二价杂环芳基团的一种;n是大于或等于2的整数。
    公开号:
    US08519150B2
  • 作为产物:
    描述:
    碳酸乙烯酯3,4-diaminothiophene dihydrochloridesodium carbonate 作用下, 以 1,3-dimethyl-2-imidazolidinone (DMI) 为溶剂, 反应 4.25h, 生成 1H-thieno[3,4-d]imidazol-2(3H)-one
    参考文献:
    名称:
    Heterocyclic fused imidazolone, dioxolone, imidazolethione and dioxolethione monomers
    摘要:
    揭示了一种制备如下式化合物的方法:其中Z为Se或S;Y为NH或O;X为O或S,W和W′从羟基,-C═ONH2,-C═ONHR′,-C═ONR′R′,-C≡N和R′为C1-6烷基的组中独立选择,以及所得的单体化合物。该方法包括将3,4-二取代噻吩或硒吩或二取代噻吩或硒吩衍生物与含有羰基或硫代羰基的化合物接触,所述化合物从尿素,硫脲,碳酸酯,硫代碳酸酯,硫代碳酸酯酯或正碳酸酯中选择。单体化合物适用于形成聚合物,用于各种电子应用。
    公开号:
    US20070282099A1
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文献信息

  • PI-ELECTRON CONJUGATED COMPOUND, MANUFACTURING METHOD THEREFOR, AND PI-ELECTRON CONJUGATED POLYMER OBTAINED USING SAME
    申请人:Kondou Yoshirou
    公开号:US20110201777A1
    公开(公告)日:2011-08-18
    Provided are a π-electron conjugated polymer having a constitutional unit represented by general formula (2) that is suitable as an electrochromic material that changes from a desired colored state to a decolored state, a new compound that is a raw material of the polymer, and a method for producing the polymer: wherein each X independently represents one selected from the group consisting of an oxygen atom, a sulfur atom, —NH—, and —NR 1 — (wherein R 1 is an optionally substituted alkyl group having 1 to 20 carbon atoms or an optionally substituted aryl group having 6 to 20 carbon atoms); each Y independently represents an oxygen atom or a sulfur atom; each Z independently represents one selected from the group consisting of a hydrogen atom and optionally substituted organic groups having 1 to 20 carbon atoms, and W is one selected from the group consisting of an ethynylene group, an optionally substituted ethenylene group, optionally substituted arylene groups, and optionally substituted divalent heteroaromatic ring groups; and n is an integer of 2 or greater.
    提供了一种π-电子共轭聚合物,其具有适用于电致变色材料的构成单元,该材料从所需的有色状态变为无色状态,一种作为该聚合物原料的新化合物以及一种制备该聚合物的方法:其中,每个X独立地表示从由氧原子、原子、—NH—和—NR1—(其中R1是具有1至20个碳原子的可选取代烷基或具有6至20个碳原子的可选取代芳基)组成的群体中选择的一个;每个Y独立地表示氧原子或原子;每个Z独立地表示从氢原子和具有1至20个碳原子的可选取代有机基团中选择的一个,W从乙炔基、可选取代的乙烯基、可选取代的芳基基团和可选取代的双价杂环芳基环组成的群体中选择一个;n为大于或等于2的整数。
  • Hydrogenation of Compounds Containing Divalent Sulfur
    作者:Ralph Mozingo、Stanton A. Harris、Donald E. Wolf、Charles E. Hoffhine、Nelson R. Easton、Karl Folkers
    DOI:10.1021/ja01228a011
    日期:1945.12
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同类化合物

沙维拉唑 4H-吡咯并[1,2-a]噻吩并[3,2-D]咪唑 3H-噻吩并[2,3-d]咪唑-5-羧酸 3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮 2-(氯甲基)-1H-噻吩并[3,4-d]咪唑 1H-噻吩并[3,2-D]咪唑-2(3H)-酮 1H-噻吩并[2,3-d]咪唑,1-乙烯基-(9CI) 1H-噻吩并(3,4-d)咪唑,2-(((5-甲基-2-吡啶基)甲基)亚硫酰基)- 1-甲基-1H-噻吩并[2,3-D]咪唑基-2(3H)-酮 1-乙烯基-1H-噻吩并[2,3-d]咪唑-5-羧酸 1,3-二氢噻吩并[3,4-d]咪唑-2-硫酮 2-(3-Chloro-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-(1-isopropyl-pyrrolo[3,2-b]pyridin-5-yl)-4-methyl-1,3-thiazole-5-carboxylic acid isopropyl ester 2-(3-cyano-1-isopropyl-pyrrolo[3,2-b]pyridin-5-yl)-4-methyl-1,3-thiazole-5-carboxylic acid isopropyl ester 2-(5-Methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-(4-ethoxy-benzyl)-1(3)H-thieno[2,3-d]imidazole 3,4,8-triamino-1H-pyrazolo<3,4-d>thieno<2,3-b>pyridin-7-carbonsaeure-ethylester 1-[2-(5-Methyl-pyridin-2-ylmethanesulfinyl)-3H-thieno[3,4-d]imidazol-6-yl]-ethanone 2-Oxo-2,3-dihydro-4-methyl-1H-thieno<3,4-d>imidazol 2-[4-(2,2,2-trifluoroethyloxy)-2-picolylsulfinyl]-4,6-dimethyl-1H-thieno[3,4-d]imidazole 1,2-dimethyl-N-{2-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]ethyl}-1H-thieno[3, 4-d]imidazole-4-carboxamide 2-[4-(2,2,3,3,3-pentafluoropropyloxy)-2-picolylsulfinyl]-4,6-dimethyl-1H-thieno[3,4-d]imidazole 2-(3-Fluoro-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-[(3-methoxypyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole 2-(5-Methyl-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole; hydrobromide 2-(3,5-Dimethyl-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole; hydrochloride ethyl 6-ethyl-1-methyl-3-(1-methylethoxy)-5-[(thiophen-2-ylcarbonyl)amino]-1H-pyrrolo[2,3-b]pyridine-2-carboxylate 1H-thieno[3,4-d]imidazol-2(3H)-one 2-(4-piperidino-3-chloro-2-picolylmercapto)-1H-thieno[3,4-d]imidazole 4,6-Dimethyl-2-(pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole; hydrochloride 2-(3-Methyl-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole; hydrochloride ethyl 2-benzylthio-1-methoxymethyl-1H-thieno<2,3-d>imidazole-5-carboxylate 2-(6-Methyl-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole; hydrochloride 2-(4-Methoxy-pyridin-2-ylmethylsulfanyl)-4,6-dimethyl-1H-thieno[3,4-d]imidazole; hydrochloride 2-(4-Ethoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole; hydrochloride 2-[(3-methylpyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole Methyl 2-oxo-1,3-dihydrothieno[3,4-d]imidazole-4-carboxylate 2-oxo-2,3-dihydro-4-(δ-N-methylcarbamidobutyl)-1H-thieno<3,4-d>imidazole methyl 2-hexylthio-4-methylthieno[3,4-d]imidazole-6-carboxylate methyl 2-butylthio-4-methylthieno[3,4-d]imidazole-6-carboxylate dimethyl 4-methyl-4H-pyrrolo[3,2-d][1,3]thiazole-2,5-dicarboxylate 2-[4-(2,2,3,3,4,4,4-heptafluorobutyloxy)-2-picolylsulfinyl]-4,6-dimethyl-1H-thieno[3,4-d]imidazole 2-(3,5-Dimethyl-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 4,6-Dimethyl-2-(pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(4-Ethoxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(4-Methoxy-pyridin-2-ylmethanesulfinyl)-4,6-dimethyl-1H-thieno[3,4-d]imidazole 2-bromo-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid amide 4-phenyl-2-(pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-bromo-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfanyl]-4-(4-methoxyphenyl)-1H-thieno[3,4-d]imidazole