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2,2,4,4-tetramethyl-[1,3]dioxolane | 13372-34-4

中文名称
——
中文别名
——
英文名称
2,2,4,4-tetramethyl-[1,3]dioxolane
英文别名
2,2,4,4-Tetramethyl-[1,3]dioxolan;2,2,4,4-Tetramethyl-1,3-dioxolan;2,2,4,4-Tetramethyldioxolane;2,2,4,4-tetramethyl-1,3-dioxolane
2,2,4,4-tetramethyl-[1,3]dioxolane化学式
CAS
13372-34-4
化学式
C7H14O2
mdl
——
分子量
130.187
InChiKey
LKXGAIPPBQYEJB-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:
    109-110 °C
  • 密度:
    0.8912 g/cm3(Temp: 15 °C)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2,2,4,4-tetramethyl-[1,3]dioxolane苯甲醛(CF3SO3)2 作用下, 以 二氯甲烷 为溶剂, 反应 8.0h, 以95%的产率得到2-phenyl-4,4-dimethyl-1,3-dioxolane
    参考文献:
    名称:
    阳离子钯(II),铂(II)和铑(I)配合物作为缩醛催化剂
    摘要:
    描述了[Pd(H 2 O)2(Ph 2 PCH 2 CH 2 PPh 2)](CF 3 SO 3)2作为催化剂用于各种醛和酮的缩醛化和反缩醛化的用途。还显示出Pt(H 2 O)2(PH 2 PCH 2 CH 2 PPh 2)(CF 3 SO 3)2至少与相应的Pd化合物一样有效,而使用[Rh (MeOH)2(Ph 2 PCH2 CH 2 PPh 2)] [BF 4 ]。
    DOI:
    10.1002/hlca.19900730317
  • 作为产物:
    描述:
    甲基环氧丙烷丙酮 在 boron fluoride ether 作用下, 生成 2,2,4,4-tetramethyl-[1,3]dioxolane
    参考文献:
    名称:
    Petrow, Zhurnal Obshchei Khimii, 1940, vol. 10, p. 981,988
    摘要:
    DOI:
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文献信息

  • [EN] NOVEL PROCESS FOR THE PREPARATION OF SPIROHETEROCYCLIC PYRROLIDINE DIONES<br/>[FR] NOUVEAU PROCÉDÉ DE PRÉPARATION DE PYRROLIDINE DIONES SPIROHÉTÉROCYCLIQUES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2015007640A1
    公开(公告)日:2015-01-22
    A process for making certain spiroheterocyclic pyrrolidine dione derivatives.
    制备某些螺环杂环吡咯烷二酮衍生物的方法。
  • [EN] 1 - AZA - SPIRO [4.5] DEC- 3 - ENE AND 1, 8 - DIAZA - SPIRO [4.5 ] DEC- 3 - ENE DERIVATIVES AS PESTICIDES<br/>[FR] DÉRIVÉS DE 1-AZA-SPIRO[4.5]DÉC-3-ÈNE ET DE 1,8-DIAZA-SPIRO[4.5]DÉC-3-ÈNE EN TANT QUE PESTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2013150015A1
    公开(公告)日:2013-10-10
    A compound of the formula (I), wherein the substituents are as defined in claim 1, are useful as a pesticides.
    式(I)的化合物,其中取代基如权利要求1所定义的那样,可用作杀虫剂。
  • Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use related applications
    申请人:NitroMed, Inc.
    公开号:US20040024057A1
    公开(公告)日:2004-02-05
    The invention describes novel nitrosated nonsteroidal antiinflammatory drugs (NSAIDs) and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated NSAID, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one nitrosated NSAID, and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one nitrosated NSAID, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating inflammation, pain and fever; for treating gastrointestinal disorders; for facilitating wound healing; for treating and/or preventing gastrointestinal, renal and/or respiratory toxicities resulting from the use of nonsteroidal antiinflammatory compounds; for treating inflammatory disease states and/or disorders; and for treating and/or preventing ophthalmic diseases and/or disorders.
    该发明描述了新型亚硝化非甾体抗炎药(NSAIDs)及其药用盐,以及包含至少一种亚硝化NSAID的新型组合物,以及可选地,至少一种提供、转移或释放一氧化氮、刺激内源性一氧化氮合成、提高内源性内皮源性舒张因子水平或是一氧化氮合酶底物的化合物,和/或至少一种治疗剂。该发明还提供了包含至少一种亚硝化NSAID和至少一种提供、转移或释放一氧化氮、提高内源性内皮源性舒张因子水平、刺激内源性一氧化氮合成或是一氧化氮合酶底物和/或至少一种治疗剂的新型组合物。该发明还提供了包含至少一种亚硝化NSAID,可选地至少一种一氧化氮供体和/或至少一种治疗剂的新型试剂盒。该发明还提供了治疗炎症、疼痛和发热的方法;治疗胃肠道疾病的方法;促进伤口愈合的方法;治疗和/或预防由非甾体抗炎化合物使用引起的胃肠道、肾脏和/或呼吸道毒性的方法;治疗炎症性疾病状态和/或疾病的方法;以及治疗和/或预防眼科疾病和/或疾病的方法。
  • 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides
    申请人:Syngenta Participations AG
    公开号:EP2647626A1
    公开(公告)日:2013-10-09
    A compound of the formula I wherein the substituents are as defined in claim 1, are useful as a pesticides.
    式I的化合物,其中取代基如权利要求书1所定义的那样,可用作杀虫剂。
  • The determination of the heats of formation of carbonyl and nitrile ylides by photoacoustic calorimetry
    作者:Joseph A. La Villa、Joshua L. Goodman
    DOI:10.1016/0040-4039(88)85243-2
    日期:——
    Using photoacoustic calorimetry, the heats of formation of the ylides 1 and 2, formed from the reaction of methylene and acetone and acetonitrile, respectively, are 4.5 and 70.8 . The heats of reaction for fragmentation of the ylides 1 and 2 are estimated to be 45 and 49 .
    使用光声量热法,由亚甲基与丙酮和乙腈的反应形成的酰化物1和2的形成热分别为4.5和70.8 。用于裂解酰基1和2的反应热估计为45和49 。
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