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12H-Benzothioxanthen-12-on | 3604-45-3

中文名称
——
中文别名
——
英文名称
12H-Benzothioxanthen-12-on
英文别名
12H-Benzo[b]thioxanthen-12-one;benzo[b]thioxanthen-12-one
12H-Benzo<b>thioxanthen-12-on化学式
CAS
3604-45-3
化学式
C17H10OS
mdl
——
分子量
262.332
InChiKey
HWRDHOQOYKQNMJ-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):
    5.2
  • 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:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    airpotassium tert-butylate 作用下, 以 四氢呋喃 为溶剂, 反应 7.0h, 以50%的产率得到12H-Benzothioxanthen-12-on
    参考文献:
    名称:
    Synthese von Benzo[b]thioxanthenen
    摘要:
    Benzo[b]thioxanthenes, heterocyclic compounds related to tetracenes and tetracyclines can be obtained by the reaction of 2H-benzo[b]thiete (1) and 1,4-naphthoquinones (3a-g). The primary cycloadducts 4a-g undergo an autoxidation process leading to the quinones 6a-g. The dihydroxy compound 4e shows an additional isomerization by a tetra-fold H transfer (4e --> 5e'). Another preparative route to benzo[b]thioxanthenes makes use of the cycloadditon reaction of 1 and 1,4-epoxynaphthalenes (7a-d). The primary adducts can be transformed to the title compounds by catalytic dehydration processes (8a-d --> 9a-d). An alternate regioselective opening of the oxygen bridge can be performed by the action of trimethyliodosilane (8a --> 10a). Methylation of 9a furnishes the sulfonium salt 14a which rearranges in a strongly alkaline medium to 16a; in the presence of oxygen ketone 17a is generated.
    DOI:
    10.1002/prac.19953370181
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文献信息

  • Oxime Ester Photoinitiators
    申请人:Matsumoto Akira
    公开号:US20090087759A1
    公开(公告)日:2009-04-02
    Compounds of the formula (I), (II), and wherein R 1 , R 2 , R′ 2 and R′″ 2 for example are C 1 -C 20 alkyl; R 3 , R 4 , and R 5 for example independently of one another are hydrogen or a defined substituent provided that at least one of R 3 , R 4 or R 5 is other than hydrogen or C 1 -C 20 alkyl; R 6 , R 7 , R 8 , R′ 6 , R′ 7 , R′ 8 , R″ 6 , R″ 7 , R′″6 and R′″7 for example independently of one another have one of the meanings as given for R 3 , R 4 , and R 5 ; and R 9 for example is C 1 -C 20 alkyl; exhibit an unexpectedly good performance in photopolymerization reactions.
    式(I)、(II)和中的化合物,其中R1、R2、R′2和R′″2例如为C1-C20烷基;R3、R4和R5例如分别独立地为氢或定义的取代基,只要R3、R4或R5中至少有一个不是氢或C1-C20烷基;R6、R7、R8、R′6、R′7、R′8、R″6、R″7、R′″6和R′″7例如分别独立地具有R3、R4和R5所给出的含义之一;而R9例如为C1-C20烷基;在光聚合反应中表现出意外的良好性能。
  • OXIME ESTER PHOTOINITIATORS
    申请人:Matsumoto Akira
    公开号:US20100086881A1
    公开(公告)日:2010-04-08
    Compounds of the formula (I), wherein A 1 is formula (II); A 2 is formula (III); A 3 is formula (IV); A 4 is formula (V); w, x, y and z independently of each other are an integer from 0-4, provided that the sum of x+y+z is an integer from 2-4, corresponding to the valency of Q; M 1 , M 2 , M 3 and M 4 for example are a direct bond, CO or O; Y for example is a direct bond or S; Q is a (x+y)-valent linking group; R 1 is for example hydrogen, C 1 -C 20 alkyl or phenyl or naphthyl; R 2 and R″ 2 for example are is hydrogen or C 1 -C 20 alkyl; R 3 , R 4 , R′ 3 , R′ 4 , R″ 3 and R″ 4 for example are hydrogen, halogen, phenyl, or C 1 -C 20 alkyl; and R 24 is for example a direct bond; exhibit an unexpectedly good performance in photopolymerization reactions.
    公式(I)化合物,其中A1为公式(II); A2为公式(III); A3为公式(IV); A4为公式(V); w、x、y和z相互独立,均为0-4之间的整数,前提是x+y+z的总和为2-4之间的整数,对应于Q的价态; M1、M2、M3和M4例如为直接键,CO或O; Y例如为直接键或S; Q为(x+y)-价联结基; R1例如为氢、C1-C20烷基或苯基或萘基; R2和R″2例如为氢或C1-C20烷基; R3、R4、R′3、R′4、R″3和R″4例如为氢、卤素、苯基或C1-C20烷基; R24例如为直接键; 在光聚合反应中表现出意外的良好性能。
  • Oxime ester photoinitiators
    申请人:BASF SE
    公开号:EP2172455A1
    公开(公告)日:2010-04-07
    Compounds of the formula II, and III wherein R1, R2, R'2 and R"'2 for example are C1-C20alkyl; R3, R4, and R5 for example independently of one another are hydrogen or a defined substituent provided that at least one of R3, R4 or R5 is other than hydrogen or C1-C20alkyl; R6, R7, R8, R'6, R'7, R'8, R"6, R"7, R"'6 and R"'7 for example independently of one another have one of the meanings as given for R3, R4, and R5; and R9 for example is C1-C20alkyl; exhibit an unexpectedly good performance in photopolymerization reactions.
    式 II 和 III 的化合物 其中 R1、R2、R'2 和 R"'2 例如为 C1-C20 烷基;R3、R4 和 R5 例如相互独立地为氢或定义的取代基,条件是 R3、R4 或 R5 中至少有一个不是氢或 C1-C20 烷基;R6、R7、R8、R'6、R'7、R'8、R "6、R "7、R"'6 和 R"'7(例如各自独立地)具有 R3、R4 和 R5 所给出的含义之一;以及 R9(例如 C1-C20 烷基)在光聚合反应中表现出意想不到的良好性能。
  • US8349548B2
    申请人:——
    公开号:US8349548B2
    公开(公告)日:2013-01-08
  • US8524425B2
    申请人:——
    公开号:US8524425B2
    公开(公告)日:2013-09-03
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