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7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene

中文名称
——
中文别名
——
英文名称
7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene
英文别名
7-Propyl-3,11-dithia-5,7,9-triazatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene;7-propyl-3,11-dithia-5,7,9-triazatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene
7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene化学式
CAS
——
化学式
C9H9N3S2
mdl
——
分子量
223.323
InChiKey
XBWMWPHBPVSFLW-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):
    3.1
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    87.2
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    描述:
    7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene四(三苯基膦)钯正丁基锂 作用下, 以 四氢呋喃 为溶剂, 生成 2-cyano-3-(5-{5-[5-(2,2-dicyanovinyl)thiophen-2-yl]-7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalen-2-yl}thiophen-2-yl)acrylonitrile
    参考文献:
    名称:
    Evaporable organic semiconductive material and use thereof in an optoelectronic component
    摘要:
    这项发明涉及一般式IIIa的化合物及其在光电子元件中的应用。
    公开号:
    US09127020B2
  • 作为产物:
    描述:
    7-propyl-2,5-bis(triisopropylsilanyl)-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 在 四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 生成 7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene
    参考文献:
    名称:
    Evaporable organic semiconductive material and use thereof in an optoelectronic component
    摘要:
    这项发明涉及一般式IIIa的化合物及其在光电子元件中的应用。
    公开号:
    US09127020B2
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文献信息

  • EVAPORABLE ORGANIC SEMICONDUCTIVE MATERIAL AND USE THEREOF IN AN OPTOELECTRONIC COMPONENT
    申请人:Hildebrandt Dirk
    公开号:US20130167930A1
    公开(公告)日:2013-07-04
    The invention relates to compounds of general formula IIIa and their use in optoelectronic components.
    本发明涉及通式IIIa化合物及其在光电组件中的使用。
  • VERDAMPFBARES ORGANISCH HALBLEITENDES MATERIAL UND DESSEN VERWENDUNG IN EINEM OPTOELEKTRONISCHEN BAUELEMENT
    申请人:Heliatek GmbH
    公开号:EP2483267B9
    公开(公告)日:2014-05-14
  • US9127020B2
    申请人:——
    公开号:US9127020B2
    公开(公告)日:2015-09-08
  • Evaporable organic semiconductive material and use thereof in an optoelectronic component
    申请人:Hildebrandt Dirk
    公开号:US09127020B2
    公开(公告)日:2015-09-08
    The invention relates to compounds of general formula IIIa and their use in optoelectronic components.
    这项发明涉及一般式IIIa的化合物及其在光电子元件中的应用。
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同类化合物

4H-吡咯并[2.3-d][1,3]噻唑-5-羧酸乙酯 4H-吡咯并[2,3-d]噻唑-5-羧酸 4H-吡咯并[2,3-d]噻唑 (7aS)-1-(1-cyanoethenyl)tetrahydro-1H,3H-pyrrolo[1,2-c]thiazole-3-thione 4-methyl-4,6-dihydro-5H-thiazolo[5‘,4‘:4,5]pyrrolo[2,3-d]pyridazin-5-one 3-((2,4-dimethyl-5-oxo-4H-thiazolo[5’,4’:4,5]pyrrolo[2,3-d]pyridazin-6(5H)-yl)methyl)benzonitrile 7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 7-propyl-2,5-bis(trimethylstannyl)-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 4-methyl-4H-pyrrolo[2,3-d]thiazole-5-carboxylic acid 3-morpholino-4-(2,4,5-trimethyl-4H-pyrrolo[3,2-d][1,3]thiazol-6-yl)cyclobut-3-ene-1,2-dione (S)-3-thia-1-azabicyclo[3.3.0]octan-2-one 3,3-dioxide methyl 4H-pyrrolo[2,3-d]thiazole-5-carboxylate (4H-pyrrolo[2,3-d]thiazol-5-yl)methanol 5-methyl-4H-pyrrolo[2,3-d]thiazole tert-butyl 2-amino-4H-pyrrolo[3,2-d]thiazole-4-carboxylate 2-ethoxycarbonylamino-4-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid methyl ester (4-methyl-6-nitro-4H-pyrrolo[2,3-d]thiazol-2-yl)-carbamic acid ethyl ester 2-ethoxycarbonylamino-4-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid ethyl ester (5-bromo-4-methyl-6-nitro-4H-pyrrolo[3,2-d]thiazol-2-yl)-carbamic acid ethyl ester 2-Ethoxycarbonylamino-4-methylpyrrolo<3,2-d>thiazol (Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine (5-bromo-4-methyl-6-nitro-4H-pyrrolo[2,3-d]thiazol-2-yl)-carbamic acid ethyl ester ethyl 2-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylate ethyl 5-methyl-5H-pyrrolo[3,4-d]thiazolo-2-carboxylate 2-phenyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid ethyl ester 5-benzyl-4H-pyrrolo[2,3-d]thiazole 4-(4H-pyrrolo[2,3-d]thiazol-5-yl)pyridin-2-ylamine ethyl 4H-pyrrolo[3,2-d]thiazole-5-carboxylate 2,6-dibromo-4-(2-octyldodecyl)-4H-pyrrolo[3,2-d:4,5-d]bisthiazole tetrahydro-pyrrolo[1,2-c]thiazole-3-thione (-)-(1R,7aS)-1-methyltetrahydropyrrolo[1,2-c]thiazol-3(1H)-thione (-)-(1S,7aS)-1-methyltetrahydropyrrolo[1,2-c]thiazol-3(1H)-thione methyl (2R,6R,7R,8S,11R)-5-oxo-11-phenyl-10-thia-1-azatricyclo[6.3.0.02,6]undecane-7-carboxylate (2R,6R,7R,8S,11R)-11-phenyl-7-[(E)-2-phenylethenyl]-10-thia-1-azatricyclo[6.3.0.02,6]undecan-5-one N-[[4-(propan-2-ylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(pyridin-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(morpholine-4-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(thiophen-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(pyridin-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(morpholine-4-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(cyclopropylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(furan-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(pyrrolidine-1-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide (1S,2S,7S,8R)-10-[2-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]ethyl]-7-[(E)-2-phenylethenyl]-4-thia-6,10-diazatricyclo[6.3.0.02,6]undecane-9,11-dione (1S,2S,7R,8R)-10-[2-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]ethyl]-7-[(E)-2-phenylethenyl]-4-thia-6,10-diazatricyclo[6.3.0.02,6]undecane-9,11-dione 4-[(3,4-Dichlorophenyl)methyl]pyrrolo[2,3-d][1,3]thiazole-5-carboxylic acid 2-(4H-pyrrolo[2,3-d][1,3]thiazol-5-yl)acetic acid Methyl 4-(3,4-dichlorobenzyl)-2-methyl-4 H-pyrrolo[3,2-d ][1,3]thiazole-5-carboxylate Ethyl 4-[(3,4-dichlorophenyl)methyl]pyrrolo[2,3-d][1,3]thiazole-5-carboxylate methyl 4-(3,4-dichlorobenzyl)-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxylate