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4-(2-phenyl-1,3-dioxolan-2-yl)butyl heptanoate | 381295-00-7

中文名称
——
中文别名
——
英文名称
4-(2-phenyl-1,3-dioxolan-2-yl)butyl heptanoate
英文别名
——
4-(2-phenyl-1,3-dioxolan-2-yl)butyl heptanoate化学式
CAS
381295-00-7
化学式
C20H30O4
mdl
——
分子量
334.456
InChiKey
IWZFSRPRDHLHOZ-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):
    4.6
  • 重原子数:
    24
  • 可旋转键数:
    12
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    盐酸4-(2-phenyl-1,3-dioxolan-2-yl)butyl heptanoate乙酸乙酯氯化钠Sodium sulfate-III 、 SiO2 、 Diethylether heptane 作用下, 以 四氢呋喃 为溶剂, 反应 24.0h, 以Column chromatography (SiO2, heptane/ether 8:2) afforded 2.74 g (73%) of a colourless oil, which的产率得到5-oxo-5-phenylpentyl heptanoate
    参考文献:
    名称:
    Ketones as precursors of active compounds
    摘要:
    该化合物的化学式为其中Y代表吡啶基或式中的苯基,其中R3代表氢原子、CF3基团或烷氧基团,R4代表氢原子、烷基或CF3基团,R5代表氢原子、烷基、CF3基团或烷氧基团,而R1和R2则是式中末端烯烃的取代基,其中R1代表烷基或烷基烯基、单环或多环脂环基或含有氧、氮、磷或硫等一些杂原子的苯基,而R2代表氢原子、烷基或烷基烯基、单环或多环脂环基或含有氧、氮、磷或硫等一些杂原子的苯基。该化合物能够在光照作用下释放出活性化合物,例如香水,可以优势地用于处理任何表面,通过控制香气分子的释放来使其香气。
    公开号:
    US06949680B2
点击查看最新优质反应信息

文献信息

  • UTILISATION OF KETONES AS PRECURSORS OF ACTIVE COMPOUNDS
    申请人:FIRMENICH SA
    公开号:EP1294671A2
    公开(公告)日:2003-03-26
  • US6949680B2
    申请人:——
    公开号:US6949680B2
    公开(公告)日:2005-09-27
  • [EN] UTILISATION OF KETONES AS PRECURSORS OF ACTIVE COMPOUNDS<br/>[FR] UTILISATION DE CÉTONES COMME PRÉCURSEURS DE COMPOSÉS ACTIFS
    申请人:FIRMENICH & CIE
    公开号:WO2001096272A2
    公开(公告)日:2001-12-20
    A compound of formula (I) wherein Y represents a pyridyl group, or a phenyl group of formula [formula (Ia)] wherein R3 represents a hydrogen atom, a CF3 group or a linear or branched alkoxy group from C1 to C12, R4 represents a hydrogen atom, a linear or branched alkyl group from C1 to C4, or a CF3 group, R5 represents a hydrogen atom, a linear or branched alkyl group from C1 to C4, a CF3 group or a linear or branched alkoxy group from C1 to C12; and R1 and R2 are the substituents of a terminal alkene of formula (i) wherein R1 represents a linear or branched alkyl or alkylene group from C1 to C35, an unsubstituted or substituted mono- or poly-cycloalkyl group having 3 to 8 carbon atoms, or an unsubstituted or substituted phenyl group, said alkyl, alkylene, mono- or poly-cycloalkyl and phenyl groups possibly comprising one or several hetero-atoms selected from the group consisting of oxygen, nitrogen, phosphorous and sulphur; and R2 represents a hydrogen atom, a linear or branched alkyl or alkylene group from C1 to C35, an unsubstituted or substituted mono- or poly-cycloalkyl group from C3 to C8, or an unsubstituted or substituted phenyl group, said alkyl, alkylene, mono- or poly-cycloalkyl and phenyl groups possibly comprising one or several hetero-atoms selected from the group consisting of oxygen, nitrogen, phosphorous and sulphur ; is capable of releasing, upon an exposure to light, an active compound such as a perfume and can be advantageously used in the treatment of any surface in order to perfume it through the controlled releasse of a perfumed molecule.
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