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2-氧代-1-噁螺[4.4]壬烷-4-羧酸 | 18363-10-5

中文名称
2-氧代-1-噁螺[4.4]壬烷-4-羧酸
中文别名
——
英文名称
2-oxo-1-oxaspiro<4,4>nonan-4-carboxylic acid
英文别名
2-oxo-1-oxa-spiro[4.4]nonane-4-carboxylic acid;2-Oxo-1-oxa-spiro[4.4]nonan-4-carbonsaeure;2-oxo-1-oxaspiro[4.4]nonane-4-carboxylic acid;γ,γ-Tetramethylenparaconsaeure
2-氧代-1-噁螺[4.4]壬烷-4-羧酸化学式
CAS
18363-10-5
化学式
C9H12O4
mdl
MFCD00461592
分子量
184.192
InChiKey
RHSJEQPXBBAWME-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:
    430.3±38.0 °C(Predicted)
  • 密度:
    1.32±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.777
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2932209090

SDS

SDS:30e7220957e5378e53b148cf33b99653
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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
  • 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:
    参考文献:
    名称:
    使用1,3-二碘-5,5-二甲基乙内酰脲通过对锥酸和β-羧基 -γ-丁内酰胺的脱羧碘化,方便地合成α,β-不饱和γ-丁内酯和γ-丁内酰胺†
    摘要:
    开发了一种简便的合成方法,合成α,β-不饱和γ-丁内酯和α,β-不饱和γ-丁内酰胺。该反应通过在辐射下使用1,3-二碘-5,5-二甲基乙内酰脲(DIH)对对苯二甲酸和β-羧基-γ-丁内酰胺进行脱羧碘化,然后对β-碘-γ-丁内酯和γ-进行加氢碘化来进行。丁内酰胺可提供高产率的α,β-不饱和γ-丁内酯和γ-丁内酰胺,它们是有机合成中合成有用的组成部分。
    DOI:
    10.1039/c5ob01574j
  • 作为产物:
    描述:
    2-oxo-1-oxaspiro<4,4>nonan-3,4-dicarboxylic acid diethyl ester盐酸 作用下, 反应 5.0h, 以35%的产率得到2-氧代-1-噁螺[4.4]壬烷-4-羧酸
    参考文献:
    名称:
    Synthesis of new derivatives of carbo(hetero)cyclospirobutanoic lactones
    摘要:
    DOI:
    10.1007/bf01171302
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文献信息

  • COSMETIC OR DERMATOLOGICAL COMPOSITION COMPRISING A POLYMER BEARING JUNCTION GROUPS, AND COSMETIC TREATMENT PROCESS
    申请人:Chodorowski-Kimmes Sandrine
    公开号:US20100239509A1
    公开(公告)日:2010-09-23
    The present patent application relates to a cosmetic or dermatological composition comprising, in a cosmetically or dermatologically acceptable medium, a polymer comprising: (a) a polymer backbone that may be obtained by reaction: of a polyol comprising 3 to 6 hydroxyl groups; of a monocarboxylic acid containing 6 to 32 carbon atoms; of a polycarboxylic acid comprising at least two carboxylic groups COOH, and/or of a cyclic anhydride such as a polycarboxylic acid and/or of a lactone comprising at least one carboxylic group COOH; and (b) at least one junction group linked to the said polymer backbone and capable of establishing H bonds with one or more partner junction groups, each pairing of a junction group involving at least three H (hydrogen) bonds. The patent application also concerns a cosmetic treatment process using the said composition.
    本专利申请涉及一种化妆品或皮肤科学组合物,包括在化妆品或皮肤科学上可接受的介质中,包含以下聚合物的组合物:(a) 由以下反应得到的聚合物骨架:含有3至6个羟基的多元醇;含有6至32个碳原子的一元羧酸;至少含有两个羧基COOH的多元羧酸,和/或类似多元羧酸的环酐和/或至少含有一个羧基COOH的内酯;以及(b) 至少一个连接到所述聚合物骨架的连接基团,并能够与一个或多个配对连接基团建立H键,每个连接基团的配对涉及至少三个H(氢)键。该专利申请还涉及使用所述组合物的化妆品处理过程。
  • COMPOSITION COMPRISING A POLYCONDENSATE, METHOD OF TREATMENT, POLYCONDENSATE, AND METHOD OF PREPARATION
    申请人:GIUSTINIANI Pascal
    公开号:US20090028807A1
    公开(公告)日:2009-01-29
    The present application relates to a cosmetic or pharmaceutical, in particular lipstick, composition comprising a polycondensate The application also relates to a method of cosmetic treatment using the composition, the polycondensate thus defined and a method of preparing the polycondensate.
    本申请涉及一种化妆品或药用品,特别是口红,包括聚缩酸酯的组合物。该申请还涉及一种使用该组合物进行化妆处理的方法,所述聚缩酸酯的定义以及一种制备聚缩酸酯的方法。
  • COSMETIC OR PHARMACEUTICAL COMPOSITION COMPRISING A POLYCONDENSATE, THE SAID POLYCONDENSATE AND METHOD OF COSMETIC TREATMENT
    申请人:Malle Gerard
    公开号:US20100272660A1
    公开(公告)日:2010-10-28
    The present application relates to a cosmetic or pharmaceutical composition comprising a polycondensate capable of being obtained by the reaction of the following monomers alone: of 10 to 30% by weight, relative to the total weight of the polycondensate, of one or more polyols comprising 3 to 6 hydroxyl groups; of 30 to 80% by weight, relative to the total weight of the polycondensate, of one or more linear, branched and/or cyclic, saturated or unsaturated, non-aromatic monocarboxylic acids comprising 6 to 32 carbon atoms; of 1 to 40% by weight, relative to the total weight of the polycondensate, of one or more polycarboxylic acids and/or cyclic anhydrides of such a polycarboxylic acid and/or lactones comprising at least one COOH group; and optionally of 0.1 to 15% by weight, relative to the total weight of the polycondensate, of one or more silicones having a hydroxyl and/or carboxyl functional group. The application also relates to a method of cosmetic treatment using the said composition, and the polycondensate thus defined.
    本申请涉及一种化妆品或药用组合物,包括由以下单体反应而得的聚缩酸酯:相对于聚缩酸酯的总重量,占10至30%的一种或多种含有3至6个羟基的多元醇;占30至80%的一种或多种线性、支链和/或环状、饱和或不饱和、非芳香族的单羧酸,含有6至32个碳原子;占聚缩酸酯总重量的1至40%的一种或多种多羧酸和/或多羧酸的环状酐和/或含有至少一个COOH基团的内酯;以及可选地占聚缩酸酯总重量的0.1至15%的一种或多种硅氧烷,具有羟基和/或羧基官能团。该申请还涉及使用所述组合物进行化妆处理的方法,以及如此定义的聚缩酸酯。
  • Silver-Mediated Decarboxylative Fluorination of Paraconic Acids: A Direct Entry to β-Fluorinated γ-Butyrolactones
    作者:Supasorn Phae-nok、Darunee Soorukram、Chutima Kuhakarn、Vichai Reutrakul、Manat Pohmakotr
    DOI:10.1002/ejoc.201500023
    日期:2015.5
    silver(I)-mediated decarboxylative fluorination of paraconic acids using Selectfluor® as a fluorine source is reported. Readily available paraconic acids undergo decarboxylative fluorination with Selectfluor® mediated by AgNO3 to give the corresponding β-fluorinated γ-butyrolactones in moderate to good yields. This approach serves as a direct and site-selective strategy for the introduction of a fluorine atom at
    报道了使用 Selectfluor® 作为氟源对对康酸进行银 (I) 介导的脱羧氟化。容易获得的对康酸通过 Selectfluor® 在 AgNO3 介导下进行脱羧氟化,以中等至良好的产率得到相应的 β-氟化 γ-丁内酯。这种方法可作为在 γ-丁内酯核的 β 位置引入氟原子的直接和位点选择性策略。氟化产物是合成有用的有机合成支架。
  • Decarboxylation of Paraconic Acids by a Silver(I) Nitrate/Persulfate Combination: An Entry to β-Nitro- and β-Hydroxy γ-Butyrolactones
    作者:Darunee Soorukram、Supasorn Phae-nok、Chutima Kuhakarn、Pawaret Leowanawat、Vichai Reutrakul
    DOI:10.1055/a-1792-7169
    日期:2022.9
    Decarboxylative transformations of paraconic acids, a class of γ-butyrolactones containing a carboxylic acid group at the β-position as their characteristic functionality, by using a combination of AgNO3/K2S2O8 were investigated. The dual function of AgNO3 as an initiator of the decarboxylation process and as a source of nitrogen dioxide radicals that react with aliphatic carboxylic substrates is reported
    通过使用AgNO 3 /K 2 S 2 O 8的组合,研究了对康酸(一类在β-位含有羧酸基团作为其特征官能团的γ-丁内酯)的脱羧转化。AgNO 3的双重功能作为脱羧过程的引发剂和作为与脂肪族羧酸底物反应的二氧化氮自由基的来源首次被报道。从仲康酸开始,在一锅操作中以中等的选择性获得了良好的综合收率 (41-85%) 的 β-硝基和 β-羟基 γ-丁内酯。在γ-丁内酯核可耐受的温和条件下,反应在可接受的反应时间(两小时)内完成。本研究提供了对 β-硝基和 β-羟基 γ-丁内酯的直接和位点特异性入口,它们是有机转化中的重要前体。
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