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5-(N-p-Toluenesulfonyl)iminothianthrene | 19615-38-4

中文名称
——
中文别名
——
英文名称
5-(N-p-Toluenesulfonyl)iminothianthrene
英文别名
5-(N-p-tosyl)iminothianthrene;4-methyl-N-thianthren-5-ylidenebenzenesulfonamide
5-(N-p-Toluenesulfonyl)iminothianthrene化学式
CAS
19615-38-4
化学式
C19H15NO2S3
mdl
——
分子量
385.532
InChiKey
YQTSDQSVJKPMCS-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

  • 沸点:
    595.2±53.0 °C(Predicted)
  • 密度:
    1.40±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.2
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    111
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:356c7642a4e53f9bc25cbfda5bfde345
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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

  • 作为反应物:
    描述:
    5-(N-p-Toluenesulfonyl)iminothianthrene1,4-二溴丁烷 作用下, 反应 2.0h, 以40%的产率得到噻蒽
    参考文献:
    名称:
    Nagasawa, Kazuo; Yoneta, Akemi; Sugimoto, Hideki, Chemical and pharmaceutical bulletin, 1987, vol. 35, # 10, p. 4351 - 4354
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    Photo SN-bond cleavage and related reactions of thianthrene sulfilimine derivatives
    摘要:
    Several 1- and 2-substituted thianthrene sulfilimine derivatives were prepared and the selectivity toward oxidation and N-tosylimination under several conditions was studied. In the photolysis of trans-5-(N-p-tosyl) iminothianthrene 10-oxide (trans-10), photo isomerization to cis-10 was observed. Further, photoimino-transferreaction of sulfilimines and their 10-mono- and -dioxide derivatives to sulfides was intensively studied to make clear the ability as nitrene precursors. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.05.004
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文献信息

  • Syntheses and Structural Analysis of 10-Monoxy- and -Dioxy-5-N-Substituted Iminothianthrene Derivatives and the Stereochemical Change on their Sulfur Atom under Acidic and Thermal Conditions
    作者:Hiroyuki Morita、Hiroyuki Kawaguchi、Toshiaki Yoshimura、Eiichi Tsukurimichi、Choichiro Shimasaki、Ernst Horn
    DOI:10.1002/1521-3765(20001103)6:21<3976::aid-chem3976>3.0.co;2-5
    日期:2000.11.3
    5-(N-p-Tolulnesulfonyl)iminothianthrenes, whose sulfur atoms are oxidized to a sulfoxide or sulfone at the 10-position. were hydrolysed readily in high yield to N-unsubstituted-suifilimines by using concentrated H2SO4. During hydrolysis, 10-monoxy-5-N-unsubstituted-sulfilimines were obtained as a separable mixture of the cis and trims isomers. The stereochemical interconversion of these compounds was studied under both hydrolytic and thermal conditions and their structures were elucidated by using X-ray crystallography.
  • Alkaline hydrolysis of N-bromoiminothianthrene derivatives
    作者:Hiroyuki Kawaguchi、Akitaka Nakajima、Takayoshi Fujii、Bung Ju Kim、Junko Hashimoto、Akihiro Fujimoto、Toshiaki Yoshimura、Hiroyuki Morita
    DOI:10.1016/j.tet.2006.08.087
    日期:2006.11
    5-(N-Bromo)iminothianthrene (2) and 5-(N-bromo)iminothianthrene 10-oxide (5) and 10,10-dioxide (8) were prepared and their alkaline hydrolyses were studied. The compound 2 and cis-5-(N-bromo)iminothianthrene 10-oxide (cis-5) afforded the corresponding sulfoximine exclusively. While, unexpectedly, both trans-5-(N-bromo)iminothianthrene 10-oxide (trans-5) and 8 afforded mainly de-brominated products, trans-5-iminothianthrene 10-oxide (trans-4) and 5-iminothianthrene 10,10-dioxide (7), respectively. In these cases, 5-iminothianthrene 5, 10-dioxide (6) (Z- and E-mixture) and 5-iminothianthrene 5, 10, 1 0-trioxide (9) and further de-iminated products were also formed respectively as minor products. The stereochemical considerations on the S-N reactions are described in view of the steric effect and 'flip-flap' motion of the thianthrene framework. (c) 2006 Elsevier Ltd. All rights reserved.
  • Nagasawa, Kazuo; Yoneta, Akemi; Sugimoto, Hideki, Chemical and pharmaceutical bulletin, 1987, vol. 35, # 10, p. 4351 - 4354
    作者:Nagasawa, Kazuo、Yoneta, Akemi、Sugimoto, Hideki、Ito, Keiichi
    DOI:——
    日期:——
  • Photo SN-bond cleavage and related reactions of thianthrene sulfilimine derivatives
    作者:Tomoyuki Fujita、Hideo Kamiyama、Yasushi Osawa、Hiroyuki Kawaguchi、Bung Ju Kim、Atsushi Tatami、Wataru Kawashima、Tetsuo Maeda、Atsushi Nakanishi、Hiroyuki Morita
    DOI:10.1016/j.tet.2007.05.004
    日期:2007.8
    Several 1- and 2-substituted thianthrene sulfilimine derivatives were prepared and the selectivity toward oxidation and N-tosylimination under several conditions was studied. In the photolysis of trans-5-(N-p-tosyl) iminothianthrene 10-oxide (trans-10), photo isomerization to cis-10 was observed. Further, photoimino-transferreaction of sulfilimines and their 10-mono- and -dioxide derivatives to sulfides was intensively studied to make clear the ability as nitrene precursors. (c) 2007 Elsevier Ltd. All rights reserved.
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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