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4-nitrobenzyl-4'-hydroxyphenylthioether | 636602-05-6

中文名称
——
中文别名
——
英文名称
4-nitrobenzyl-4'-hydroxyphenylthioether
英文别名
4-(4-nitro-benzylsulfanyl)-phenol;4-(4-Nitro-benzylmercapto)-phenol;4-[(4-nitrophenyl)methylsulfanyl]phenol
4-nitrobenzyl-4'-hydroxyphenylthioether化学式
CAS
636602-05-6
化学式
C13H11NO3S
mdl
MFCD13171701
分子量
261.301
InChiKey
UBYNIVOARSNLHH-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:
    469.9±35.0 °C(Predicted)
  • 密度:
    1.37±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.076
  • 拓扑面积:
    91.4
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 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:
    4-nitrobenzyl-4'-hydroxyphenylthioether 在 bismuth(III) chloride 、 钾硼氢 作用下, 以 乙醇 为溶剂, 反应 4.5h, 生成 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-difluoro-5-hydroxy-6b-(2-hydroxy-acetyl)-4a,6a-dimethyl-8-[4-(4-hydroxy-phenylsulfanylmethyl)-phenyl]-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,11,12-tetradecahydro-7-oxa-8-aza-pentaleno[2,1-a]phenanthren-2-one
    参考文献:
    名称:
    ISOXAZOLIDINE DERIVATIVES
    摘要:
    根据此处定义的公式(I),糖皮质类固醇系列的抗炎和抗过敏化合物对于治疗呼吸道疾病特别有效,这些疾病以气道阻塞为特征。
    公开号:
    US20120238531A1
  • 作为产物:
    描述:
    4-羟基苯硫酚对硝基溴化苄potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 12.0h, 以62%的产率得到4-nitrobenzyl-4'-hydroxyphenylthioether
    参考文献:
    名称:
    Correspondence between Molecular Functionality and Crystal Structures. Supramolecular Chemistry of a Family of Homologated Aminophenols
    摘要:
    The crystal structures and packing features of a family of 13 aminophenols, or supraminols, are analyzed and correlated. These compounds are divided into three groups: (a) compounds 1-5 with methylene spacers of the general type HO-C6H4-(CH2)(n)-C6H4-NH2 (n = 1 to 5) and both OH and NH2 in a para position; (b) compounds 1 a, 2a, 2b, 2c, and 3a in which one or more of the methylene linkers in 1 to 3 are exchanged with an S-atom; and (c) compounds 2d, 1b, and 6a prepared with considerations of crystal engineering and where the crystal structures may be anticipated on the basis of structures 1-5, 1 a, 2a, 2b, 2c, and 3a. These 13 aminols can be described in terms of three major supramolecular synthons based on hydrogen bonding between OH and NH2 groups: the tetrameric loop or square motif, the infinite N(H)O chain, and the beta-As sheet. These three synthons are not completely independent of each other but interrelate, with the structures tending toward the more stable beta-As sheet in some cases. Compounds 1-5 show an alternation in melting points, and compounds with n = even exhibit systematically higher melting points compared to those with n = odd. The alternating melting points are reflected in, and explained by, the alternation in the crystal structures. The n = odd structures tend toward the beta-As sheet as n increases and can be considered as a variable series whereas for n = even, the beta-As sheet is invariably formed constituting a fixed series. Substitution of a methylene group by an isosteric S-atom may causes a change in the crystal structure. These observations are rationalized in terms of geometrical and chemical effects of the functional groups. This study shows that even for compounds with complex crystal structures the packing may be reasonably anticipated provided a sufficient number of examples are available.
    DOI:
    10.1021/ja037227p
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文献信息

  • Leandri; Tundo, Bollettino Scientifico della Facolta di Chimica Industriale di Bologna, 1956, vol. 14, p. 31
    作者:Leandri、Tundo
    DOI:——
    日期:——
  • [EN] ISOXAZOLIDINE DERIVATIVES<br/>[FR] DÉRIVÉS D'ISOXAZOLIDINE
    申请人:CHIESI FARMA SPA
    公开号:WO2012123493A9
    公开(公告)日:2013-01-31
  • US8835412B2
    申请人:——
    公开号:US8835412B2
    公开(公告)日:2014-09-16
  • Correspondence between Molecular Functionality and Crystal Structures. Supramolecular Chemistry of a Family of Homologated Aminophenols
    作者:Venu R. Vangala、Balakrishna R. Bhogala、Archan Dey、Gautam R. Desiraju、Charlotte K. Broder、Philip S. Smith、Raju Mondal、Judith A. K. Howard、Chick C. Wilson
    DOI:10.1021/ja037227p
    日期:2003.11.1
    The crystal structures and packing features of a family of 13 aminophenols, or supraminols, are analyzed and correlated. These compounds are divided into three groups: (a) compounds 1-5 with methylene spacers of the general type HO-C6H4-(CH2)(n)-C6H4-NH2 (n = 1 to 5) and both OH and NH2 in a para position; (b) compounds 1 a, 2a, 2b, 2c, and 3a in which one or more of the methylene linkers in 1 to 3 are exchanged with an S-atom; and (c) compounds 2d, 1b, and 6a prepared with considerations of crystal engineering and where the crystal structures may be anticipated on the basis of structures 1-5, 1 a, 2a, 2b, 2c, and 3a. These 13 aminols can be described in terms of three major supramolecular synthons based on hydrogen bonding between OH and NH2 groups: the tetrameric loop or square motif, the infinite N(H)O chain, and the beta-As sheet. These three synthons are not completely independent of each other but interrelate, with the structures tending toward the more stable beta-As sheet in some cases. Compounds 1-5 show an alternation in melting points, and compounds with n = even exhibit systematically higher melting points compared to those with n = odd. The alternating melting points are reflected in, and explained by, the alternation in the crystal structures. The n = odd structures tend toward the beta-As sheet as n increases and can be considered as a variable series whereas for n = even, the beta-As sheet is invariably formed constituting a fixed series. Substitution of a methylene group by an isosteric S-atom may causes a change in the crystal structure. These observations are rationalized in terms of geometrical and chemical effects of the functional groups. This study shows that even for compounds with complex crystal structures the packing may be reasonably anticipated provided a sufficient number of examples are available.
  • ISOXAZOLIDINE DERIVATIVES
    申请人:GHIDINI Eleonora
    公开号:US20120238531A1
    公开(公告)日:2012-09-20
    Anti-inflammatory and antiallergic compounds of the glucocorticosteroid series according to formula (I) defined herein are useful for treating diseases of the respiratory tract characterized by airway obstruction.
    根据此处定义的公式(I),糖皮质类固醇系列的抗炎和抗过敏化合物对于治疗呼吸道疾病特别有效,这些疾病以气道阻塞为特征。
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