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3,3',5,5',6,6'-hexamethyl-2,2'-trithiobishydroquinone | 125714-64-9

中文名称
——
中文别名
——
英文名称
3,3',5,5',6,6'-hexamethyl-2,2'-trithiobishydroquinone
英文别名
2-[(2,5-Dihydroxy-3,4,6-trimethylphenyl)trisulfanyl]-3,5,6-trimethylbenzene-1,4-diol
3,3',5,5',6,6'-hexamethyl-2,2'-trithiobishydroquinone化学式
CAS
125714-64-9
化学式
C18H22O4S3
mdl
——
分子量
398.568
InChiKey
CYZDMMLNJLKQSA-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:
    25
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    157
  • 氢给体数:
    4
  • 氢受体数:
    7

反应信息

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文献信息

  • 1, 3-Benzoxathiole derivatives, their use and their preparation
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0157603A2
    公开(公告)日:1985-10-09
    Compounds of formula (I): in which: R1 represents a hydrogen atom, an alkyl group, a substituted alkyl group, a C2-C6 alkenyl group, an aryl group, a substituted aryl group or a (C1-C6 alkoxycarbonyl group; R2 represents a hydrogen atom, a C1-C6 alkyl group or a C3 or C4 alkenyl group; R3 represents a hydrogen atom or a C1-C6 alkyl group; R4 represents a hydroxy group, a C1-C21 aliphatic acyloxy group or an aromatic acyloxy group; R5 represents a C1-C12 alkyl group, a C1-C6 alkoxy group, a hydroxy group, a C1-C7 aliphatic acyloxy group or an aromatic acyloxy group; R6 represents a hydrogen atom, a C1-C6 alkyl group or a C1-C6 alkoxy group; and n is 0, 1, or 2; and pharmaceutically acceptable salts thereof are valuable in the treatment of circulatory disorders and allergies.
    式(I)化合物: 其中 R1 代表氢原子、烷基、取代的烷基、C2-C6 烯基、芳基、取代的芳基或 C1-C6 烷氧基羰基; R2 代表氢原子、C1-C6 烷基或 C3 或 C4 烯基; R3 代表氢原子或 C1-C6 烷基;R4 代表羟基、C1-C21 脂肪族酰氧基或芳香族酰氧基; R5 代表 C1-C12 烷基、C1-C6 烷氧基、羟基、C1-C7 脂肪族酰氧基或芳香族酰氧基; R6 代表氢原子、C1-C6 烷基或 C1-C6 烷氧基;以及 n 是 0、1 或 2; 及其药学上可接受的盐类在治疗循环系统疾病和过敏症方面具有重要价值。
  • Studies on hindered phenols and analogs. 2. 1,3-Benzoxathioles having SRS-A inhibiting activity
    作者:Yuichi Aizawa、Tsutomu Kanai、Kazuo Hasegawa、Takeshi Yamaguchi、Yoshio Iizuka、Teiki Iwaoka、Takao Yoshioka
    DOI:10.1021/jm00167a032
    日期:1990.5
    A series of hindered phenolic 1,3-benzoxathioles (7a-l) were prepared and investigated for biological properties. Many compounds had LPO-lowering, antisuperoxide inhibiting, SRS-A inhibiting, and 5-lipoxygenase inhibiting activities. Among them, 5-hydroxy-4,6,7-trimethyl-2-propyl-1,3-benzoxathiole (7d) and 3-(5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiol-2-yl)propanol (7j) were most potent in SRS-A inhibiting and 5-lipoxygenase inhibiting activities, respectively, and were selected for further development as candidate drugs for the treatment of asthma.
  • YOSHIOKA, TAKAO;KITAZAWA, EIICHI;YAMAZAKI, MITSUO;IIZUKA, YOSHIO
    作者:YOSHIOKA, TAKAO、KITAZAWA, EIICHI、YAMAZAKI, MITSUO、IIZUKA, YOSHIO
    DOI:——
    日期:——
  • JOSIOKA, TAKAO;KITADZAVA, EHJITI;YAMADZAKI, MITSURO;IITSUKA, JOSIO
    作者:JOSIOKA, TAKAO、KITADZAVA, EHJITI、YAMADZAKI, MITSURO、IITSUKA, JOSIO
    DOI:——
    日期:——
  • US4691027A
    申请人:——
    公开号:US4691027A
    公开(公告)日:1987-09-01
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