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1-isopropoxynonyl hydroperoxide | 544715-82-4

中文名称
——
中文别名
——
英文名称
1-isopropoxynonyl hydroperoxide
英文别名
1-Hydroperoxy-1-propan-2-yloxynonane
1-isopropoxynonyl hydroperoxide化学式
CAS
544715-82-4
化学式
C12H26O3
mdl
——
分子量
218.337
InChiKey
WHNOKOGPBWFFNG-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

物化性质

  • 沸点:
    297.3±23.0 °C(Predicted)
  • 密度:
    0.918±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    15
  • 可旋转键数:
    10
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    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:
    1-isopropoxynonyl hydroperoxidecalcium hypochlorite 作用下, 以 乙腈 为溶剂, 反应 0.17h, 以93%的产率得到壬酸异丙酯
    参考文献:
    名称:
    Fragmentation of chloroperoxides: hypochlorite-mediated dehydration of hydroperoxyacetals to esters
    摘要:
    Hypochlorites efficiently dehydrate hydroperoxyacetals to furnish the corresponding esters. The reaction, which can be accomplished with stoichometric Ca(OCl)(2) or with catalytic amounts of t-BuOCl, appears to involve formation and heterolytic fragmentation of secondary chloroperoxides, species not previously described in solution chemistry. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.08.068
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文献信息

  • Re<sub>2</sub>O<sub>7</sub>-catalyzed reaction of hemiacetals and aldehydes with <i>O</i>-, <i>S-,</i> and <i>C</i>-nucleophiles
    作者:Wantanee Sittiwong、Michael W Richardson、Charles E Schiaffo、Thomas J Fisher、Patrick H Dussault
    DOI:10.3762/bjoc.9.174
    日期:——
    monothioacetalization and allylation of hemiacetals. The reactions, which take place under mild conditions and at low catalyst loadings, can be conducted using hemiacetals, the corresponding O-silyl ethers, and, in some cases, the acetal dimers. Aldehydes react under similar conditions to furnish good yields of dithioacetals. Reactions of hemiacetals with nitrogen nucleophiles are unsuccessful. 1,2-Dioxolan-3-ols
    Re(VII) 氧化物催化半缩醛缩醛化、单过氧缩醛化、单缩醛化和烯丙基化。在温和条件和低催化剂负载下发生的反应可以使用半缩醛、相应的 O-甲硅烷基醚以及在某些情况下使用缩醛二聚体进行。醛在类似条件下反应以提供良好收率的二缩醛半缩醛与含氮亲核试剂的反应不成功。1,2-Dioxolan-3-ols(过氧半缩醛)进行 Re(VII) 促进的醚化,但不进行烯丙基化。氢过氧缩醛(1-烷氧基氢过氧化物)在 Re2O7 或布朗斯台德酸存在下进行醇盐基团的选择性交换。
  • Oil ozonolysis
    申请人:Fitchett Stanley Colin
    公开号:US20050010069A1
    公开(公告)日:2005-01-13
    Ozonolysis is a well known process involving reacting ozone with alkene compounds, for example in unsaturated vegetable oils or free fatty acids and esters thereof, to form ozonolysis products (e.g. ozonides). The invention concerns ozonolysis of unsaturated oils (e.g. unsaturated plant oils and/or unsaturated animal oils) in the presence of a participating co-reactant to form reaction products particularly suitable for use in the formation of resins.
    臭氧分解是一种众所周知的工艺,涉及臭氧与烯烃化合物(例如不饱和植物油或游离脂肪酸及其酯类中的烯烃化合物)反应,形成臭氧分解产物(例如臭氧化物)。本发明涉及不饱和油(如不饱和植物油和/或不饱和动物油)在参与共反应物存在下的臭氧分解,以形成特别适用于树脂形成的反应产物。
  • OIL OZONOLYSIS
    申请人:Cambridge Biopolymers Limited
    公开号:EP1453799A1
    公开(公告)日:2004-09-08
  • [EN] OIL OZONOLYSIS<br/>[FR] OZONOLYSE D'HUILES
    申请人:CAMBRIDGE BIOPOLYMERS LTD
    公开号:WO2003050081A1
    公开(公告)日:2003-06-19
    Ozonolysis is a well known process involving reacting ozone with alkene compounds, for example in unsaturated vegetable oils or free fatty acids and esters thereof, to form ozonolysis products (e.g. ozonides). The invention concerns ozonolysis of unsaturated oils (e.g. unsaturated plant oils and/or unsaturated animal oils) in the presence of a participating co-reactant to form reaction products particularly suitable for use in the formation of resins.
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