摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,2-dimethoxythioxanthen-9-one | 123251-37-6

中文名称
——
中文别名
——
英文名称
1,2-dimethoxythioxanthen-9-one
英文别名
1,2-dimethoxy-thioxanthen-9-one;1,2-Dimethoxy-thioxanthen-9-on;1,2-dimethoxy-9H-thioxanthen-9-one
1,2-dimethoxythioxanthen-9-one化学式
CAS
123251-37-6
化学式
C15H12O3S
mdl
——
分子量
272.324
InChiKey
LZAPWMRTQFPWQE-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):
    3.4
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    60.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] THIOXANTHONE DERIVATIVES, COMPOSITION COMPRISING THE SAME AND PATTERN FORMING METHOD COMPRISING SAID COMPOSITION<br/>[FR] DÉRIVÉS DE THIOXANTHONE, COMPOSITION LES COMPRENANT ET PROCÉDÉ DE FORMATION DE MOTIFS COMPRENANT LADITE COMPOSITION
    申请人:LINTFIELD LTD
    公开号:WO2020016389A1
    公开(公告)日:2020-01-23
    Latent photoinitiator compounds are described, as well as compositions containing such compounds and their uses in photoinitated methods for producing photoresist structures.
    描述了潜在的光引发剂化合物,以及含有这种化合物的组合物,以及它们在用于生产光刻胶结构的光引发方法中的用途。
  • Regioselective syntheses of substituted thioxanthen- and selenoxanthen-9-one derivatives.
    作者:Mitsuaki WATANABE、Mutsuhiro DATE、Masao TSUKAZAKI、Sunao FURUKAWA
    DOI:10.1248/cpb.37.36
    日期:——
    Various methoxy-substituted thioxanthen-9-one derivatives were regioselectively synthesized by a one-pot condensation of S-lithiated thiosalicylic ester or amides, obtained via directed lithiation of tertiary benzamides, with benzynes. Similarly, the synthesis of selenoxanthen-9-ones was achieved.
    通过对三级苯甲酰胺进行定向石碳酸化而得到的 S-石碳酸化硫代水杨酸酯或酰胺与苄基化合物进行一锅缩合,从而选择性地合成了各种甲氧基取代的硫杂蒽-9-酮衍生物。同样,还实现了硒氧杂蒽-9-酮的合成。
  • A METHOD FOR CLEAVAGE OF LABILE FUNCTIONAL GROUPS FROM CHEMICAL COMPOUNDS
    申请人:Universität Konstanz
    公开号:EP1480927A2
    公开(公告)日:2004-12-01
  • THIOXANTHONE DERIVATIVES, COMPOSITION COMPRISING THE SAME AND PATTERN FORMING METHOD COMPRISING SAID COMPOSITION
    申请人:Lintfield Limited
    公开号:EP3824349A1
    公开(公告)日:2021-05-26
  • Method for cleavage of labile functional groups from chemical compounds
    申请人:Steiner Ulrich
    公开号:US20050255403A1
    公开(公告)日:2005-11-17
    The present invention provides a method for cleavage of labile functional groups from molecules by the action of electromagnetic radiation, wherein the molecules are contacted with a chemical compound whose triplet state is energetically higher than the triplet state of the labile functional group, and are subsequently exposed to electromagnetic radiation. Further, the invention provides a method for preparing DNA chips by spatially addressed, light-controlled nucleotide synthesis on solid substrates, said method comprising the following steps: a) reacting the unprotected terminal 3′ or 5′ hydroxy croup of a nucleoside and/or of a nucleotide arranged on the solid substrate under usual conditions with a photolabile protective group and optionally purifying the reaction product. b) applying a solution, suspension or dispersion of a chemical compound, whose triplet state is energetically higher than the triplet state of the photolabile protective group. to the surface of the carrier, said surface comprising the nucleotides and/or nucleosides modified in step a): c) irradiating, in a spatially selective manner, the surface of the carrier treated in step b) with electromagnetic radiation in the UV/VIS range with simultaneous, spatially selective release of a reactive OH group and subsequently reacting it with a nucleoside and/or nucleotide comprising a 5′ or 3′OH group, said nucleoside and/or nucleotide being further provided with a photolabile functional group. Moreover, the present invention provides a chemical composition comprising a molecule having a labile functional group, as well as a chemical compound whose triplet state is higher than the triplet state of the labile functional group, and it describes the use of the chemical composition for preparing DNA chips.
查看更多

同类化合物

贝恩酮盐酸盐 苯并噻喃并[4,3-b]吲哚 苯并[e][1]苯并噻喃并[4,3-b]吲哚 苯并[c]噻吨-7-酮 苯并[a]噻吨-12-酮 硫坎酮 硫代色烯-2-酮 海蒽酮甲磺酸盐 海蒽酮N-甲基氨基甲酸酯 海恩酮 异丙基硫代呫吨酮 噻吨酮-3-甲酰胺 [[(9-氧代-9H-噻吨-2-基)甲基]硫代]乙酸 N-[2-(二甲氨基)乙基]-9-羰基-9H-硫代占吨-4-甲酰胺 N,N-二甲基-N'-4H-硫代色烯-4-基酰亚胺基甲酰胺 N'-[4-(羟基甲基)-9-氧代-9H-噻吨-1-基]-N,N-二乙基乙烷-1,2-二胺N-氧化物 9-氧代噻吩-4-羧酸乙酯 9-氧代噻吨-1-羧酸甲酯 9-氧代-9h-硫代氧杂蒽-2-羧酸 9-氧代-9h-硫代氧杂蒽-2-羧酸 9-氧代-9H-硫代氧杂蒽-1-羧酸 9-氧代-9H-噻吨-3-甲腈 9-氧代-9H-噻吨-2-羧酸乙酯 9-氧代-3-(苯基磺酰基)-9H-噻吨-1-羧酸乙酯 9-噻吨酮 8H-苯并噻喃并[7,8-D][1,3]噻唑 8H-苯并噻喃并[6,7-D][1,3]噻唑 8-甲基-4H-硫色烯-4-酮 8-氯-N,N-二乙基-5-甲基-2H-[1]苯并噻喃并[4,3,2-cd]吲唑-2-乙胺N-氧化物 8-氯-5-甲基-N,N-二乙基-2H-[1]苯并噻喃并[4,3,2-cd]吲唑-2-乙烷-1-胺 8-氯-5-(羟基甲基)-N,N-二乙基-2H-[1]苯并噻喃并[4,3,2-cd]吲唑-2-乙烷-1-胺N-氧化物 7H-苯并噻喃并[6,5-d][1,3]噻唑 7-甲氧基-2-甲基-4H-硫代色烯-4-酮 7-甲基-9-氧代噻吨-3-羧酸乙酯 7-氨基-1-[[2-(二乙胺)乙基]氨基]-4-甲基-L-9H-噻吨-9-酮 6H-苯并噻喃并[7,6-D][1,3]噻唑 6-甲氧基-2-甲基-4H-硫代色烯-4-酮 6-甲基-4H-硫代色烯-4-酮 6-氯-1-({2-[乙基(2-羟基乙基)氨基]乙基}氨基)-4-(羟甲基)-9H-硫代占吨-9-酮 6-氟-4H-硫代色烯-4-酮 6-氟-2-(三氟甲基)-9H-噻吨-9-酮 6-(2-二乙基氨基乙胺)-1,2,3,4-四氢苯并[a]噻吨-12-酮 5-[(2-氨基乙基)氨基]-2-[2-(二乙基氨基)乙基]-2H-苯并噻喃并[4,3,2-Cd]吲唑-8-醇三盐酸盐 5-(2-二乙基氨基乙胺)-1,2,3,4-四氢苯并[c]噻吨-7-酮 4H-1-苯并噻喃-4-酮 1,1-二氧化物 4-羟基硫代香豆素 4-甲基-9H-噻吨-9-酮 4-氯-9H-噻吨-9-酮 4-氯-3-硝基硫代香豆素 4-氯-2H-1-苯并噻喃-3-甲醛