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2-thianthrenecarboxylic acid | 14812-70-5

中文名称
——
中文别名
——
英文名称
2-thianthrenecarboxylic acid
英文别名
thianthrene-2-carboxylic acid;Thianthren-2-carbonsaeure;Thianthren-carbonsaeure-(2);Thianthren-carbonsaeure-2;Thianthren-2-carbosaeure
2-thianthrenecarboxylic acid化学式
CAS
14812-70-5
化学式
C13H8O2S2
mdl
——
分子量
260.337
InChiKey
BLJIAZIZIXSNJZ-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):
    3.7
  • 重原子数:
    17
  • 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:
    87.9
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2-thianthrenecarboxylic acid双氧水溶剂黄146 作用下, 生成 9,10-Tetraoxo-thianthren-2-carbonsaeure
    参考文献:
    名称:
    Metalation of Thianthrene-5-dioxide by n-Butyllithium and by Phenyllithium and Cleavage of Thianthrene-5,5,10-trioxide by n-Butyllithium
    摘要:
    DOI:
    10.1021/ja01558a055
  • 作为产物:
    描述:
    参考文献:
    名称:
    Metalation of Thianthrene-5-dioxide by n-Butyllithium and by Phenyllithium and Cleavage of Thianthrene-5,5,10-trioxide by n-Butyllithium
    摘要:
    DOI:
    10.1021/ja01558a055
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文献信息

  • [EN] PYRANONES USEFUL AS ATM INHIBITORS<br/>[FR] PYRANONES UTILES COMME INHIBITEURS DE L'ATM
    申请人:KUDOS PHARM LTD
    公开号:WO2003070726A1
    公开(公告)日:2003-08-28
    The application concerns a compound of formula I: (I) wherein one of P and Q is O, and the other of P and Q is H, where there is a double bond between whichever of Q and P is CH and the carbon atom bearing the R3 group;Y is either O or S;R1 and R2 are independently hydrogen, an optionally substituted C1-7 alkyl group, C3-20 heterocyclyl group, or C5-20 aryl group, or may together form an optionally substituted heterocyclic ring having from 4 to 8 ring atoms;R3 is a phenyl or pyridyl group, attached by a first bridge group selected from -S-, -S (=O)-, -S(=O)2-, -O-, -NRN- and CRC1RC2- to an optionally substituted C5-20 carboaryl group, the phenyl or pyridyl group and optionally substituted C5-20 carboaryl group being optionally further linked by a second bridge group, so as to form an optionally substituted C5-7 ring, the phenyl or pyridyl group being further optionally substituted.
    该应用涉及一种具有化学式I的化合物:(I)其中P和Q中的一个是O,另一个是H,在Q和P中的哪一个是CH和带有R3基团的碳原子之间存在双键;Y可以是O或S;R1和R2独立地是氢,可选的取代C1-7烷基,C3-20杂环基团或C5-20芳基团,或者可以共同形成具有4至8个环原子的可选取代杂环环;R3是连接到可选取代的C5-20碳基芳基基团的苯基或吡啶基团,该苯基或吡啶基团通过第一桥基团(选自-S-,-S(=O)-,-S(=O)2-,-O-,-NRN-和CRC1RC2-)连接,苯基或吡啶基团和可选取代的C5-20碳基芳基基团可以通过第二桥基团进一步连接,以形成可选取代的C5-7环,苯基或吡啶基团可以进一步取代。
  • Bennett et al., Journal of the Chemical Society, 1937, p. 444
    作者:Bennett et al.
    DOI:——
    日期:——
  • EP0755458A4
    申请人:——
    公开号:EP0755458A4
    公开(公告)日:2000-07-26
  • ELECTROGENERATED CHEMILUMINESCENCE LABELS FOR ANALYSIS AND/OR REFERENCING
    申请人:IGEN, INC.
    公开号:EP0755458A1
    公开(公告)日:1997-01-29
  • PYRANONES USEFUL AS ATM INHIBITORS
    申请人:Kudos Pharmaceuticals Limited
    公开号:EP1485377A1
    公开(公告)日:2004-12-15
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同类化合物

硅烷,1,9-硫杂蒽二基二[三甲基- 甲硫芬 噻蒽-2-硼酸 噻蒽-1,9-二甲酸 噻蒽 5-氧化物 噻蒽 5,10-二氧化物 噻蒽 噻吩-1-羧酸 噻吩-1-硼酸 六氟磷酸1-氯-5-苯基-硫杂蒽-5-正离子 二甲基噻蒽 2-溴噻蒽 2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮 2,7-噻蒽二甲酸 2,7-二氟噻蒽 2,7-二乙酰基噻蒽 2,3,7,8-四甲基-1,4,6,9-噻蒽四酮 2,3,7,8-四氯噻蒽 1,4,6,9-噻蒽四酮 2,7-bis(9-carbazolyl)thianthrene 1,7-dimethylthianthrene 13,13,14,14-Tetracyano-2-methylbenzonaphtho<2,3-e><1,4>dithiin-6,11-quinodimethane 2-methyl-5,12-dithianaphthacene 13,13,14,14-Tetracyanobenzonaphtho<2,3-e><1,4>dithiin-6,11-quinodimethane 2,5-dihexylbenzo[5,6][1,4]dithiino[2,3-e]pyrrolo[3,4-g]isoindole-1,3,4,6(2H,5H)-tetraone 2-cyanothianthrene 1-cyanothianthrene 2,3-difluorothianthrene 3-(1-thianthrenyl)phenol 2,7-diisopropylthianthrene-5,5,10,10-tetraoxide (Z)-2-(5-thianthreniumyl)-2-hexene perchlorate (E)-2-(5-thianthreniumyl)-2-hexene perchlorate (Z)-3-(5-thianthreniumyl)-2-hexene perchlorate (E)-3-(5-thianthreniumyl)-2-hexene perchlorate Phenylthianthren-2-ylmethanol 1,1′-methylenedithianthrene 1,1′-(chloromethylene)dithianthrene 1,6-dithianthren-1-ylhexane-1,6-diol 9-(4-methylacetophenone)thianthrenium perchlorate Thianthren-1-ylphenylmethanol Diphenylthianthren-1-ylmethanol 4,4,5,5-tetramethyl-2-(thianthren-2-yl)-1,3,2-dioxaborolane thianthrene-2-sulfonic acid 2-(thianthren-1-ylsulfanyl)pyridine 2,8-dibromothianthrene dithianthren-1-ylmethanol 5-(2-acetamido-4,5-dimethylphenyl)thianthreniumyl perchlorate 5-(4-anisyl)thianthreniumyl perchlorate 1-tributylstannylthianthrene 5-(3-bromo-4-methoxyphenyl)thianthreniumyl perchlorate