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7-amino-6-chloro-4-phenylquinolin-2-one | 769954-16-7

中文名称
——
中文别名
——
英文名称
7-amino-6-chloro-4-phenylquinolin-2-one
英文别名
7-amino-6-chloro-4-phenylquinol-2-one;7-amino-6-chloro-4-phenyl-1H-quinolin-2-one
7-amino-6-chloro-4-phenylquinolin-2-one化学式
CAS
769954-16-7
化学式
C15H11ClN2O
mdl
——
分子量
270.718
InChiKey
WKWJEMJLFOOVTD-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):
    2.5
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    55.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    7-amino-6-chloro-4-phenylquinolin-2-one盐酸 、 sodium nitrite 作用下, 以 溶剂黄146 为溶剂, 反应 1.5h, 生成
    参考文献:
    名称:
    [EN] BISAZOQUINOLONE PIGMENTS, PROCESSES FOR THEIR PREPARATION AND THEIR USE
    [FR] PIGMENTS DE BISAZOQUINOLONE, PREPARATION ET UTILISATION
    摘要:
    Bisazoquinolone颜料,其中在其互变异构形式之一中,对应于式(1),其中W是未取代或取代的C6-C24芳基的基团或未取代或取代的杂芳基的基团,Ar1是未取代或取代的C6-C24芳基或未取代或取代的杂芳基,Ar11是未取代或取代的C6-C24芳基或未取代或取代的杂芳基,R1、R2、R10、R11和R12各自独立地是氢、C1-C6烷基、卤素、氰基、CF3、硝基、NR3R4、COOR4、NR4COR3、COOX+、COR4、OR4、SR3、SO2R3、SO2NR3R4、SO3-X+,或未取代或由R5单独或多取代的C6-C24芳基,R3是C1-C6烷基,或未取代或由卤素、羟基、OR7、氰基、硝基、SR7、NR6R7、COOR7、CONR6R7、NR6COR7、NR6COOR7、COO-X+、COR4、OR4、SO2R7、SO2NR6R7、SO3-X+或由SO3R7单独或多取代的C6-Cl2芳基,R4是氢或具有与R3相同的含义,R5是氢、C1-C4烷基、卤素、硝基、NR7R8或OR7,R6是氢或C1-C3烷基,R7和R8各自独立地是氢、C1-C3烷基、未取代或由卤素、硝基、OR5或由NR16R17取代的苯基,或未取代或由卤素、硝基、OR5或由NR16R17取代的苄基,X+是H+、Li+、Na+、K+、Mg++1/2、Ca++1/2、Sr++1/2、Ba++1/2、Cu+、Cu++1/2、Zn++1/2、Mn++1/2、Al+++1/3或[NR19R20R21R22]+其中R19、R20、R21和R22各自独立地是氢、C1-C6烷基、未取代或由C1-C6烷基、卤素、硝基、OR5或由NR16R17取代的苯基,或未取代或由C1-C6烷基、卤素、硝基、OR5或由NR16R17取代的苄基,R16和R17各自独立地是氢或C1-C6烷基,Z1是-NH-或-0-,Z2是-NH或-0-,适用于着色高分子量材料,并以所得的色彩具有良好的耐久性特性而著称。
    公开号:
    WO2004111134A1
  • 作为产物:
    描述:
    4-氯-1,3-苯二胺苯甲酰乙酸乙酯吡啶对甲苯磺酸 作用下, 以 xylene 为溶剂, 反应 11.0h, 以88%的产率得到7-amino-6-chloro-4-phenylquinolin-2-one
    参考文献:
    名称:
    [EN] MONOAZOQUINOLONE PIGMENTS, PROCESS FOR THEIR PREPARATION AND THEIR USE
    [FR] PIGMENTS DE MONOAZOQUINOLONE, LEUR PROCEDE DE PREPARATION ET LEUR UTILISATION
    摘要:
    单氮基喹啉酮颜料,在它们的互变异构形式之一中,对应于式(1),其中W是未取代或取代的C6-C24芳基或未取代或取代的杂环芳基,或是式(1a)中的基团,其中Ar2是未取代或取代的C6-C24芳基或未取代或取代的杂环芳基,Ar1是未取代或取代的C6-C24芳基或未取代或取代的杂环芳基,R、R1和R2分别独立地是氢、C1-C6烷基、卤素、氰基、CF3、硝基、NR3R4、COOR4、NR4COR3、COO-X+、COR4、OR4、SR3、S02R3、SO2NR3R4、SO3-X+或未取代或经R5单取代或多取代的C6-C24芳基,R3是C1-C6烷基,或未取代或经卤素、羟基、OR7、氰基、硝基、SR7、NR6R7、COOR7、CONR6R7、NR6COR7、NR6COOR7、COO-X+、COR4、OR4、SO2R7、SO2NR6R7、SO3-X+或S03R7单取代或多取代的C6-C12芳基,R4是氢或具有R3的含义,R5是氢、C1-C4烷基、卤素、硝基、NR7R8或OR7,R6是氢或C1-C3烷基,R7和R8分别独立地是氢、C1-C3烷基、未取代或经卤素、硝基、OR5、NR16R17单取代或多取代的苯基,或未取代或经卤素、硝基、OR5、NR16R17单取代或多取代的苄基,X+是H+、Li+、Na+、K+、Mg++1/2、Ca++1/2、Sr++1/2、Ba++1/2、Cu+、Cu++1/2、Zn++1/2、Mn++1/2、Al+++1/3或[NR9R10R11R12]+,其中R9、R10、R11和R12分别独立地是氢、C1-C6烷基、未取代或经C1-C6烷基、卤素、硝基、OR5、NR16R17单取代或多取代的苯基,或未取代或经C1-C6烷基、卤素、硝基、OR5、NR16R17单取代或多取代的苄基,R16和R17分别独立地是氢或C1-C6烷基,适用于高分子量材料的着色,并以所得色彩的良好牢度特性而著称。
    公开号:
    WO2004085540A1
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文献信息

  • Monoazoquinolone pigments, process for their preparation and their use
    申请人:Benkhoff Johannes
    公开号:US20060219134A1
    公开(公告)日:2006-10-05
    Monoazoquinolone pigments which, in one of their tautomeric forms, correspond to formula (1), wherein W is unsubstituted or substituted C 6 -C 24 aryl or unsubstituted or substituted heteroaryl or is a radical of formula (1a), wherein Ar 2 is unsubstituted or substituted C 6 -C 24 aryl or unsubstituted or substituted heteroaryl, Ar 1 is unsubstituted or substituted C 6 -C 24 aryl or unsubstituted or substituted heteroaryl, R, R 1 , and R 2 are each independently of the others hydrogen, C 1 -C 6 alkyl, halogen, cyano, CF 3 , nitro, NR 3 R 4 , COOR 4 , NR 4 COR 3 , COO − X + , COR 4 , OR 4 , SR 3 , SO 2 R 3 , SO 2 NR 3 R 4 , SO 3 −X + , or C 6 -C 24 aryl which is unsubstituted or mono- or polysubstituted by R 5 , R 3 is C 1 -C 6 alkyl, or C 6 -C 12 aryl which is unsubstituted or mono- or poly-substituted by halogen, hydroxy, OR 7 , cyano, nitro, SR 7 , NR 6 R 7 , COOR 7 , CONR 6 R 7 , NR 6 COR 7 , NR 6 COOR 7 , COO − X + , COR 4 , OR 4 , SO 2 R 7 , SO 2 NR 6 R 7 , SO 3 − X + or by SO 3 R 7 , R 4 is hydrogen or has the meanings of R 3 , R 5 is hydrogen, C 1 -C 4 alkyl, halogen, nitro, NR 7 R 8 or OR 7 , R 6 is hydrogen or C 1 -C 3 alkyl, R 7 and R 8 are each independently of the other hydrogen; C 1 -C 3 alkyl; phenyl which is unsubstituted or mono- or poly-substituted by halogen, nitro, OR 5 , NR 16 R 17 ; or benzyl which is unsubstituted or mono- or poly-substituted by halogen, nitro, OR 5 , NR 16 R 17 , and X + is a cation H + , Li + , Na + , K + , Mg ++ 1/2 , Ca ++ 1/2 , Sr ++ 1/2 , Ba ++1/2 , Cu + , Cu ++ 1/2 , Zn ++ 1/2 , Mn ++ 1/2 , Al +++ 1/3 or [NR 9 R 10 R 11 R 12 ] + , wherein R 9 , R 10 , R 11 and R 12 are each independently of the others hydrogen; C 1 -C 6 alkyl; phenyl which is unsubstituted or mono- or poly-substituted by C 1 -C 6 alkyl, halogen, nitro, OR 5 , NR 16 R 17 ; or benzyl which is unsubstituted or mono- or poly-substituted by C 1 -C 6 alkyl, halogen, nitro,OR 5 , NR 16 R 17 , and R 16 and R 17 are each independently of the other hydrogen or C 1 -C 6 alkyl, are suitable for the colouring of high molecular weight material and are distinguished by good fastness properties of the resulting colourations.
    单偶氮喹啉酮颜料,其同分异构体形式之一符合式 (1),其中 W 是未取代或取代的 C 6 -C 24 芳基或未取代或取代的杂芳基,或为式 (1a) 的基团,其中 Ar 2 是未取代或取代的 C 6 -C 24 芳基或未取代或取代的杂芳基,Ar 1 是未取代或取代的 C 6 -C 24 芳基或未取代或取代的杂芳基,R、R 1 和 R 2 各自独立地为氢、C 1 -C 6 烷基、卤素、氰基、CF 3 硝基、NR 3 R 4 、COOR 4 , NR 4 COR 3 , COO - X + , COR 4 , OR 4 , SR 3 , SO 2 R 3 , SO 2 NR 3 R 4 , SO 3 -X + 或 C 6 -C 24 未被取代或被 R 5 , R 3 是 C 1 -C 6 烷基,或 C 6 -C 12 未被取代或被卤素、羟基、OR 7 、氰基、硝基、SR 7 、NR 6 R 7 , COOR 7 , CONR 6 R 7 , NR 6 COR 7 , NR 6 COR 7 , COO - X + , COR 4 , OR 4 , SO 2 R 7 , SO 2 NR 6 R 7 , SO 3 - X + 或 SO 3 R 7 , R 4 是氢或具有 R 3 , R 5 是氢、C 1 -C 4 烷基、卤素、硝基、NR 7 R 8 或 OR 7 , R 6 是氢或 C 1 -C 3 烷基,R 7 和 R 8 各自独立地为氢;C 1 -C 3 烷基;未被取代或被卤素、硝基、OR 5 、NR 16 R 17 或未被卤素、硝基、OR 5 、NR 16 R 17 和 X + 是阳离子 H + , Li + , Na + , K + , Mg ++ 1/2 , Ca ++ 1/2 , Sr ++ 1/2 钡 ++1/2 , Cu + , Cu ++ 1/2 , Zn ++ 1/2 锰 ++ 1/2 , Al +++ 1/3 或 [NR 9 R 10 R 11 R 12 ] + 其中 R 9 , R 10 , R 11 和 R 12 各自独立地为氢; C 1 -C 6 烷基;未被 C 1 -C 6 烷基、卤素、硝基、OR 5 、NR 16 R 17 或未取代的苄基,或被 C 1 -C 6 烷基、卤素、硝基、OR 5 、NR 16 R 17 和 R 16 和 R 17 各自独立地为氢或 C 1 -C 6 烷基,适用于高分子量材料的着色,并具有良好的染色牢度特性。
  • MONOAZOQUINOLONE PIGMENTS, PROCESS FOR THEIR PREPARATION AND THEIR USE
    申请人:Ciba Specialty Chemicals Holding Inc.
    公开号:EP1606352A1
    公开(公告)日:2005-12-21
  • BISAZOQUINOLONE PIGMENTS, PROCESSES FOR THEIR PREPARATION AND THEIR USE
    申请人:Ciba Specialty Chemicals Holding Inc.
    公开号:EP1633817A1
    公开(公告)日:2006-03-15
  • Bisazoquinolone pigments, processes for their preparation and their use
    申请人:Benkhoff Johannes
    公开号:US20070066724A1
    公开(公告)日:2007-03-22
    Bisazoquinolone pigments which, in one of the tautomeric forms thereof, correspond to formula (1) wherein W is the radical of an unsubstituted or substituted C 6 -C 24 aryl or the radical of an unsubstituted or substituted heteroaryl, Ar 1 is unsubstituted or substituted C 6 -C 24 aryl or unsubstituted or substituted heteroaryl, Ar 11 is unsubstituted or substituted C 6 -C 24 aryl or unsubstituted or substituted heteroaryl, R 1 R 1 , R 2 , R 10 , R 11 , and R 12 are each independently of the others hydrogen, C 1 -C 6 alkyl, halogen, cyano, CF 3 , nitro, NR 3 R 4 , COOR 4 , NR 4 COR 3 , COOX + , COR 4 , OR 4 , SR 3 , S0 2 R 3 , S0 2 NR 3 R 4 , S0 3 -X + , or C 6 -C 24 aryl unsubstituted or mono- or poly-substituted by R 5 , R 3 is C 1 -C 6 alkyl, or C 6 -C 12 aryl unsubstituted or mono- or polysubstituted by halogen, hydroxy, OR 7 , cyano, nitro, SR 7 , NR 6 R 7 , COOR 7 , CONR 6 R 7 , NR 6 COR 7 , NR 6 COOR 7 , COO—X + , COR 4 , OR 4 , S0 2 R 7 , S0 2 NR 6 R 7 , S0 3 -X + or by S0 3 R 7 , R 4 is hydrogen or has the same meanings as R 3 , R 5 is hydrogen, C 1 -C 4 alkyl, halogen, nitro, NR 7 R 8 or OR 7 , R 6 is hydrogen or C 1 -C 3 alkyl, R 7 and R 8 are each independently of the other hydrogen, C 1 -C 3 alkyl, phenyl unsubstituted or mono- or poly-substituted by halogen, nitro, OR 5 or by NR 16 R 17 , or benzyl unsubstituted or mono- or poly-substituted by halogen, nitro, OR 5 or by NR 16 R 17 , and X + is a cation H + , Li + , Na + , K + , Mg + + 1/2 , Ca ++ 1/2 , Sr ++ 1/2 , Ba ++ 1/2 , Cu + , Cu ++ 1/2 , Zn ++ 1/2 , Mn ++ 1/2 , Al +++ 1/3 or [NR 19 R 20 R 21 R 22 ] + wherein R 19 , R 20 , R 21 and R 22 are each independently of the others hydrogen, C 1 -C 6 alkyl, phenyl unsubstituted or mono- or polysubstituted by C 1 -C 6 alkyl, halogen, nitro, OR 5 or by NR 16 R 17 , or benzyl unsubstituted or mono- or poly-substituted by C 1 -C 6 alkyl, halogen, nitro, OR 5 or by NR 16 R 17 , R 16 and R 17 are each independently of the other hydrogen or C 1 -C 6 alkyl, Z 1 , is —NH— or -0-, and Z 2 is —NH or -0- are suitable for colouring high molecular weight material and are distinguished by the resulting colorations having good fastness properties.
  • [EN] BISAZOQUINOLONE PIGMENTS, PROCESSES FOR THEIR PREPARATION AND THEIR USE<br/>[FR] PIGMENTS DE BISAZOQUINOLONE, PREPARATION ET UTILISATION
    申请人:CIBA SC HOLDING AG
    公开号:WO2004111134A1
    公开(公告)日:2004-12-23
    Bisazoquinolone pigments which, in one of the tautomeric forms thereof, correspond to formula (1) wherein W is the radical of an unsubstituted or substituted C6-C24aryl or the radical of an unsubstituted or substituted heteroaryl, Ar1 is unsubstituted or substituted C6-C24aryl or unsubstituted or substituted heteroaryl, Ar11 is unsubstituted or substituted C6-C24aryl or unsubstituted or substituted heteroaryl, R1 R 1, R2, R10, R11 and R12 are each independently of the others hydrogen, C1-C6alkyl, halogen, cyano, CF3, nitro, NR3R4, COOR4, NR4COR3, COOX+, COR4, OR4, SR3, S02R3, S02NR3R4, S03-X+, or C6-C24aryl unsubstituted or mono- or poly-substituted by R5, R3 is C1-C6alkyl, or C6-Cl2aryl unsubstituted or mono- or polysubstituted by halogen, hydroxy, OR7, cyano, nitro, SR7, NR6R7, COOR7, CONR6R7, NR6COR7, NR6COOR7, COO-X+, COR4, OR4, S02R7, S02NR6R7, S03-X+ or by S03R7, R4 is hydrogen or has the same meanings as R3, R5 is hydrogen, C1-C4alkyl, halogen, nitro, NR7R8 or OR7, R6 is hydrogen or C1-C3alkyl, R7 and R8 are each independently of the other hydrogen, C1-C3alkyl, phenyl unsubstituted or mono- or poly-substituted by halogen, nitro, OR5 or by NR16R17, or benzyl unsubstituted or mono- or poly-substituted by halogen, nitro, OR5 or by NR16R17, and X+ is a cation H+, Li+, Na+, K+, Mg++1/2, Ca++1/2, Sr++1/2, Ba++1/2, Cu+, Cu++1/2, Zn++1/2, Mn++1/2, Al+++1/3 or [NR19R20R21R22]+ wherein R19, R20, R21 and R22 are each independently of the others hydrogen, C1-C6alkyl, phenyl unsubstituted or mono- or polysubstituted by C1-C6alkyl, halogen, nitro, OR5 or by NR16R17, or benzyl unsubstituted or mono- or poly-substituted by C1-C6alkyl, halogen, nitro, OR5 or by NR16R17, R16 and R17 are each independently of the other hydrogen or C1-C6alkyl, Z1 is -NH- or -0-, and Z2 is -NH or -0-, are suitable for colouring high molecular weight material and are distinguished by the resulting colorations having good fastness properties.
    Bisazoquinolone颜料,其中在其互变异构形式之一中,对应于式(1),其中W是未取代或取代的C6-C24芳基的基团或未取代或取代的杂芳基的基团,Ar1是未取代或取代的C6-C24芳基或未取代或取代的杂芳基,Ar11是未取代或取代的C6-C24芳基或未取代或取代的杂芳基,R1、R2、R10、R11和R12各自独立地是氢、C1-C6烷基、卤素、氰基、CF3、硝基、NR3R4、COOR4、NR4COR3、COOX+、COR4、OR4、SR3、SO2R3、SO2NR3R4、SO3-X+,或未取代或由R5单独或多取代的C6-C24芳基,R3是C1-C6烷基,或未取代或由卤素、羟基、OR7、氰基、硝基、SR7、NR6R7、COOR7、CONR6R7、NR6COR7、NR6COOR7、COO-X+、COR4、OR4、SO2R7、SO2NR6R7、SO3-X+或由SO3R7单独或多取代的C6-Cl2芳基,R4是氢或具有与R3相同的含义,R5是氢、C1-C4烷基、卤素、硝基、NR7R8或OR7,R6是氢或C1-C3烷基,R7和R8各自独立地是氢、C1-C3烷基、未取代或由卤素、硝基、OR5或由NR16R17取代的苯基,或未取代或由卤素、硝基、OR5或由NR16R17取代的苄基,X+是H+、Li+、Na+、K+、Mg++1/2、Ca++1/2、Sr++1/2、Ba++1/2、Cu+、Cu++1/2、Zn++1/2、Mn++1/2、Al+++1/3或[NR19R20R21R22]+其中R19、R20、R21和R22各自独立地是氢、C1-C6烷基、未取代或由C1-C6烷基、卤素、硝基、OR5或由NR16R17取代的苯基,或未取代或由C1-C6烷基、卤素、硝基、OR5或由NR16R17取代的苄基,R16和R17各自独立地是氢或C1-C6烷基,Z1是-NH-或-0-,Z2是-NH或-0-,适用于着色高分子量材料,并以所得的色彩具有良好的耐久性特性而著称。
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