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1H-二苯并[去,H]喹啉-2,7-二酮 | 31293-07-9

中文名称
1H-二苯并[去,H]喹啉-2,7-二酮
中文别名
——
英文名称
2-Hydroxy-7H-dibenzochinolin-7-on
英文别名
16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,9,11,13-heptaene-8,15-dione
1H-二苯并[去,H]喹啉-2,7-二酮化学式
CAS
31293-07-9
化学式
C16H9NO2
mdl
——
分子量
247.253
InChiKey
NHOYROCTVIDOJP-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:
    248 °C (decomp)
  • 沸点:
    650.8±55.0 °C(Predicted)
  • 密度:
    1.43±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Process for the preparation of 7-oxo-7H-dibenzo-[d e,h]-quinolin-2-ol
    申请人:Aziende Colori Nazionali Affini ACNA S.p.A.
    公开号:US04011224A1
    公开(公告)日:1977-03-08
    7-OXO-7H-dibenzo-[d e,h]-quinolin-2-ol which is useful as an intermediate in the preparation of dyestuffs is prepared by cycloisomerizing the novel compound, N-phenylacetyl phthalimide in an inert solvent and in the presence of a Friedel-Crafts catalyst to form the novel compound O-(3-hydroxy-1-isoquinolinyl)-benzoic acid which is then cyclized by dehydrating condensation to form the 7-oxo-7H-dibenzo-[d e,h]-quinolin-2-ol.
    用于染料制备中间体的7-OXO-7H-dibenzo-[d e,h]-quinolin-2-ol是通过在惰性溶剂中,在Friedel-Crafts催化剂的存在下,将新化合物N-苯乙酰邻苯二甲酰亚胺环化制备而成。然后,通过脱水缩合将新化合物O-(3-羟基-1-异喹啉基)-苯甲酸环化,形成7-氧代-7H-二苯并[d e,h]-喹啉-2-酚。
  • O-(3-hydroxy-1-isoquinolinyl)-benzoic acid
    申请人:Aziende Colori Nazionali Affini ACNA S.p.A.
    公开号:US04011227A1
    公开(公告)日:1977-03-08
    7-OXO-7H-dibenzo-[d e,h]-quinolin-2-ol which is useful as an intermediate in the preparation of dyestuffs is prepared by cycloisomerizing the novel compound, N-phenylacetyl phthalimide in an inert solvent and in the presence of a Friedel-Crafts catalyst to form the novel compound O-(3-hydroxy-1-isoquinolinyl)-benzoic acid which is then cyclized by dehydrating condensation to form the 7-oxo-7H-dibenzo-[d e,h]-quinolin-2-ol.
    本发明涉及一种用作染料制备中间体的7-OXO-7H-dibenzo-[d e,h]-quinolin-2-ol,其通过在惰性溶剂中,在Friedel-Crafts催化剂存在下环化新化合物N-苯乙酰基邻苯二甲酰亚胺,形成新化合物O-(3-羟基-1-异喹啉基)-苯甲酸,然后通过脱水缩合环化形成7-氧代-7H-二苯并[d e,h]-喹啉-2-醇。
  • Mikhailova, T. A.; Zaitsev, B. E.; Gorelik, M. V., Journal of Organic Chemistry USSR (English Translation), 1981, vol. 17, p. 703 - 710
    作者:Mikhailova, T. A.、Zaitsev, B. E.、Gorelik, M. V.
    DOI:——
    日期:——
  • GORELIK M. V.; KAZANKOV M. V.; BERNADSKIJ M. I., ZH. ORGAN. XIMII <ZORK-AE>, 1976, 12, HO 9, 2041-2042
    作者:GORELIK M. V.、 KAZANKOV M. V.、 BERNADSKIJ M. I.
    DOI:——
    日期:——
  • GORELIK M. V.; KAZANKOV M. V.; BERNADSKIJ M. I., ZH. ORGAN. XIMII, 1978, 14, HO 7, 1535-1544
    作者:GORELIK M. V.、 KAZANKOV M. V.、 BERNADSKIJ M. I.
    DOI:——
    日期:——
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同类化合物

蝙蝠葛辛 蝙蝠葛波酚碱 蝙蝠葛定 蝙蝠葛宁 山豆根波芬诺灵碱 7H-二苯并[de,H]喹啉-7-酮 6-羟基-5,10-二甲氧基-7H-二苯并[De,h]喹啉-7-酮 3-溴-1H-二苯并[去,H]喹啉-2,7-二酮 1H-二苯并[去,H]喹啉-2,7-二酮 5-methoxy-6-hydroxy-7H-dibenzo[de,h]quinolin-7-one N-(8-oxo-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2(7),3,5,9,11,13(17),14-octaen-5-yl)-3-piperidin-1-ylpropanamide 5-methoxy-4-nitro-7H-dibenzo[de,h]quinolin-7-one 5-methoxy-4-amino-1-azabenzanthrone 3-Bromo-5-methoxy-1-azabenzanthrone 5-methoxy-6-nitro-1-azabenzanthrone 5-Methoxy-2,3,7,11b-tetrahydro-1H-1-aza-benzo[de]anthracen-7-ol 2-hydroxy-3-ethoxycarbonyl-7H-dibenzoquinolin-7-one N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)-3-((2-((7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-11-yl)amino)ethyl)amino)propanamide 9-[3-(Dimethylamino)propionamido]-1-azabenzanthrone 9-[4-(Dimethylamino)butyramido]-1-azabenzanthrone N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)-2-((2-((7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-11-yl)amino)ethyl)amino)acetamide 9-(4-Pyrrolidinobutyramido)-1-azabenzanthrone 9-(Pyrrolidinoacetamido)-1-azabenzanthrone 9-[3-Pyrrolidinopropionamido]-1-azabenzanthrone 9-[(Dimethylamino)acetamido]-1-azabenzanthrone N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)-3-((3-((7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-11-yl)amino)propyl)amino)propanamide N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)-3-((3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)amino)propanamide 9-[3-(Diethylamino)propionamido]-1-azabenzanthrone 10-(2-pyrrolidinoethylamino)-7H-dibenzo[de,h]quinolin-7-one 10-(3-piperidinopropylamino)-7H-dibenzo[de,h]quinolin-7-one 10-(2-hydroxyethylamino)-7H-dibenzo[de,h]quinolin-7-one 10-(2-morpholinoethylamino)-7H-dibenzo[de,h]quinolin-7-one 10-(3-(diethylamino)propylamino)-7H-dibenzo[de,h]quinolin-7-one 3-((2-((2,3-dihydro-1H-cyclopenta[b]quinolin-9-yl)amino)ethyl)amino)-N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)propanamide 2-((2-((2,3-dihydro-1H-cyclopenta[b]quinolin-9-yl)amino)ethyl)amino)-N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)acetamide 3-((3-((2,3-dihydro-1H-cyclopenta[b]quinolin-9-yl)amino)propyl)amino)-N-(7-oxo-7H-dibenzo[de,h]quinolin-9-yl)propanamide 10-(2-(dimethylamino)ethylamino)-7H-dibenzo[de,h]quinolin-7-one 4-(2-(4-methylpiperazin-1-yl)ethoxy)-7H-dibenzo[de,h]quinolin-7-one 4-(3-(4-methylpiperazin-1-yl)propoxy)-7H-dibenzo[de,h]quinolin-7-one 2,3-dihydro-7H-dibenzo[de,h]quinolin-7-one 4-(2-(diethylamino)ethoxy)-7H-dibenzo[de,h]quinolin-7-one 4-(3-(piperidin-1-yl)propoxy)-7H-dibenzo[de,h]quinolin-7-one 4-(3-(diethylamino)propoxy)-7H-dibenzo[de,h]quinolin-7-one 5-methoxy-6-nitro-7H-dibenzo[de,h]quinolin-7-one Trimethyl-[2-[(8-oxo-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-14-yl)oxy]ethyl]azanium;iodide 14-[2-(1-Methylpiperidin-1-ium-1-yl)ethoxy]-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-8-one;iodide 14-[2-(1-Methylpyrrolidin-1-ium-1-yl)ethoxy]-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-8-one;iodide Diethyl-methyl-[2-[(8-oxo-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-14-yl)oxy]ethyl]azanium;iodide 4-Bromo-5-methoxy-1-azabenzanthrone 3-(1-methylpiperidin-1-ium-1-yl)-N-(8-oxo-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2(7),3,5,9,11,13(17),14-octaen-5-yl)propanamide;iodide