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4-methylhexa-1,4,5-trien-3-ol | 1126623-96-8

中文名称
——
中文别名
——
英文名称
4-methylhexa-1,4,5-trien-3-ol
英文别名
——
4-methylhexa-1,4,5-trien-3-ol化学式
CAS
1126623-96-8
化学式
C7H10O
mdl
——
分子量
110.156
InChiKey
OSUQOXONUUXABX-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):
    1.3
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    4-methylhexa-1,4,5-trien-3-olmanganese(IV) oxide 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 以37%的产率得到4-methylhexa-1,4,5-trien-3-one
    参考文献:
    名称:
    Synthesis of 5-Hydroxycyclopent-2-enones from Allenyl Vinyl Ketones via an Interrupted Nazarov Cyclization
    摘要:
    Treatment of an allenyl vinyl ketone with trifluoroacetic acid leads to Nazarov cyclization, and the intermediate carbocation is trapped efficiently by trifluoroacetate. Hydrolysis of the ester with methanol and basic alumina provides, in good to excellent overall yield, a 5-hydroxycyclopent-2-enone in which the alcohol is predominantly trans to a substituent at C-4.
    DOI:
    10.1021/ol900029d
  • 作为产物:
    描述:
    1-溴-2-丁炔丙烯醛indium氯化铵 作用下, 以 甲醇 为溶剂, 反应 1.0h, 以58%的产率得到4-methylhexa-1,4,5-trien-3-ol
    参考文献:
    名称:
    Synthesis of 5-Hydroxycyclopent-2-enones from Allenyl Vinyl Ketones via an Interrupted Nazarov Cyclization
    摘要:
    Treatment of an allenyl vinyl ketone with trifluoroacetic acid leads to Nazarov cyclization, and the intermediate carbocation is trapped efficiently by trifluoroacetate. Hydrolysis of the ester with methanol and basic alumina provides, in good to excellent overall yield, a 5-hydroxycyclopent-2-enone in which the alcohol is predominantly trans to a substituent at C-4.
    DOI:
    10.1021/ol900029d
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文献信息

  • [EN] COMPOSITIONS AND SYSTEMS FOR DISINFECTION<br/>[FR] COMPOSITIONS ET SYSTÈMES DE DÉSINFECTION
    申请人:PANCHERI EUGENE J
    公开号:WO2021178774A1
    公开(公告)日:2021-09-10
    A disinfectant system, comprising a first aqueous composition having a peracid reactant compound that is either a peroxide compound or an organic acid compound, and a second aqueous composition comprising the peracid reactant compound not selected for the first composition. Each composition is applied separately to, and combined upon, a surface to form a reaction layer, within which a peracid is formed in situ, disinfecting the surface. The compositions can have a flash point, surface tension, and vapor pressure compatible for application as a spray, mist, aerosol, or fog, and can be formulated with an alcohol blend that enables the reaction layer to completely evaporate from the surface after disinfection is complete. In use, the disinfectant systems disclosed herein have up to 99.999% antimicrobial efficacy against organism such as Staphylococcus aureus, Pseudomonas aeruginosa, and Candida auris.
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