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trans 1,4-diisopropoxy-2-butene | 139111-17-4

中文名称
——
中文别名
——
英文名称
trans 1,4-diisopropoxy-2-butene
英文别名
(E)-1,4-di(propan-2-yloxy)but-2-ene
trans 1,4-diisopropoxy-2-butene化学式
CAS
139111-17-4
化学式
C10H20O2
mdl
——
分子量
172.268
InChiKey
SOTWQKWPJWXFPK-AATRIKPKSA-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:
    208.2±28.0 °C(Predicted)
  • 密度:
    0.858±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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

反应信息

  • 作为反应物:
    描述:
    甲醇trans 1,4-diisopropoxy-2-butene异丙醇 以1.8 mmol of 1,3-diisopropoxy-3-butene and 9.7 mmol of cis + trans 1,4-diisopropoxy-2-butene were obtained的产率得到1,3-diisopropoxy-3-butene
    参考文献:
    名称:
    Preparation of dialkoxybutenes
    摘要:
    通过在氧气和催化有效量的固体颗粒的存在下,将1,3-丁二烯与醇反应,可以高收率地选择性制备二烷氧基丁烯。所述固体颗粒包括沉积在其支撑颗粒上的催化活性相,所述催化活性相包括至少一种第一组VIII族贵金属成分、至少一种碲、硒和/或硫第二组成分,以及可选地至少一种第三组成分,包括铋、锑、铜和/或锡。
    公开号:
    US05159120A1
  • 作为产物:
    描述:
    1-环戊烯甲醛silica gel 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 生成 乙烯trans 1,4-diisopropoxy-2-butene
    参考文献:
    名称:
    Herrmann, Wolfgang A.; Wagner, Werner; Flessner, Uwe N., Angewandte Chemie, 1991, vol. 103, # 12, p. 1704 - 1706
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Benzimidazole derivatives
    申请人:Enanta Pharmaceuticals, Inc.
    公开号:US10017499B2
    公开(公告)日:2018-07-10
    The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
    本发明公开了式(I)化合物或其药学上可接受的盐、酯或原药: 它们能抑制含 RNA 的病毒,特别是丙型肝炎病毒(HCV)。因此,本发明的化合物可干扰丙型肝炎病毒的生命周期,也可用作抗病毒药物。本发明进一步涉及包含上述化合物的药物组合物,用于给丙型肝炎病毒感染者用药。本发明还涉及通过施用包含本发明化合物的药物组合物治疗受试者感染 HCV 的方法。
  • LINKED DIBENZIMIDAZOLE DERIVATIVES
    申请人:Or Yat Sun
    公开号:US20100221214A1
    公开(公告)日:2010-09-02
    The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
  • NOVEL BENZIMIDAZOLE DERIVATIVES
    申请人:Qiu Yao-Ling
    公开号:US20100233122A1
    公开(公告)日:2010-09-16
    The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
  • HEPATITIS C VIRUS INHIBITORS
    申请人:Or Yat Sun
    公开号:US20100260715A1
    公开(公告)日:2010-10-14
    The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
  • US20140341851A1
    申请人:——
    公开号:US20140341851A1
    公开(公告)日:2014-11-20
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