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(2R)-2-[[(2R)-butan-2-yl]oxydisulfanyl]oxybutane | 1147501-45-8

中文名称
——
中文别名
——
英文名称
(2R)-2-[[(2R)-butan-2-yl]oxydisulfanyl]oxybutane
英文别名
——
(2R)-2-[[(2R)-butan-2-yl]oxydisulfanyl]oxybutane化学式
CAS
1147501-45-8
化学式
C8H18O2S2
mdl
——
分子量
210.362
InChiKey
COZUQRLRJAMOQV-HTQZYQBOSA-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:
    12
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    69.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    二氯化二硫(R)-(-)-2-丁醇三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以76%的产率得到(2R)-2-[[(2R)-butan-2-yl]oxydisulfanyl]oxybutane
    参考文献:
    名称:
    Synthesis and antimicrobial activities of structurally novel S,S′-bis(heterosubstituted) disulfides
    摘要:
    The central focus of this study is on the antibacterial and antifungal properties of synthetically produced S,S'-bis(heterosubstituted) disulfides as a means to control the growth of various infection-causing pathogens. Staphylococcus aureus, Francisella tularensis and Candida albicans were each found to be highly susceptible to several of these compounds by agar or broth dilution and Kirby-Bauer diffusion assays. These structurally simple, low molecular weight disulfides have shown promising bioactivities and may serve as leads to the development of effective new antibacterials for pathogenic bacteria such as methicillinresistant S. aureus and F. tularensis. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.04.056
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文献信息

  • Antibacterial S-heterosubstituted disulfides
    申请人:Turos Edward
    公开号:US10350177B2
    公开(公告)日:2019-07-16
    Synthetically-derived S,S-heterodisubstituted disulfides that exhibit potent in vitro antibacterial activity against a variety of bacteria, including Staphylococcus aureus, methicillin-resistant Staphylococcus aureus and Francisella tularensis. The present invention provides compounds, methods and compositions effective to treat microbial/bacterial infections, and, especially, infections arising from bacteria which have developed resistance to conventional antibiotics.
    合成衍生的 S,S-互二取代二硫化物对多种细菌(包括金黄色葡萄球菌、耐甲氧西林金黄色葡萄球菌和土拉弗氏菌)具有强效的体外抗菌活性。本发明提供了有效治疗微生物/细菌感染的化合物、方法和组合物,特别是治疗对传统抗生素产生抗药性的细菌引起的感染。
  • ANTIBACTERIAL S-HETEROSUBSTITUTED DISULFIDES
    申请人:Turos Edward
    公开号:US20100204337A1
    公开(公告)日:2010-08-12
    Synthetically-derived S,S-heterodisubstituted disulfides that exhibit potent in vitro antibacterial activity against a variety of bacteria, including Staphylococcus aureus , methicillin-resistant Staphylococcus aureus and Francisella tularensis . The present invention provides compounds, methods and compositions effective to treat microbial/bacterial infections, and, especially, infections arising from bacteria which have developed resistance to conventional antibiotics.
  • US9512160B2
    申请人:——
    公开号:US9512160B2
    公开(公告)日:2016-12-06
  • Synthesis and antimicrobial activities of structurally novel S,S′-bis(heterosubstituted) disulfides
    作者:Praveen Ramaraju、Danielle Gergeres、Edward Turos、Sonja Dickey、Daniel V. Lim、John Thomas、Burt Anderson
    DOI:10.1016/j.bmcl.2012.04.056
    日期:2012.6
    The central focus of this study is on the antibacterial and antifungal properties of synthetically produced S,S'-bis(heterosubstituted) disulfides as a means to control the growth of various infection-causing pathogens. Staphylococcus aureus, Francisella tularensis and Candida albicans were each found to be highly susceptible to several of these compounds by agar or broth dilution and Kirby-Bauer diffusion assays. These structurally simple, low molecular weight disulfides have shown promising bioactivities and may serve as leads to the development of effective new antibacterials for pathogenic bacteria such as methicillinresistant S. aureus and F. tularensis. (C) 2012 Elsevier Ltd. All rights reserved.
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