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4-isopropyl-1,3-dioxolan-2-one | 99260-49-8

中文名称
——
中文别名
——
英文名称
4-isopropyl-1,3-dioxolan-2-one
英文别名
4-(Propan-2-yl)-1,3-dioxolan-2-one;4-propan-2-yl-1,3-dioxolan-2-one
4-isopropyl-1,3-dioxolan-2-one化学式
CAS
99260-49-8
化学式
C6H10O3
mdl
——
分子量
130.144
InChiKey
JOZQZYKBYAUYOK-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:
    238.9±9.0 °C(Predicted)
  • 密度:
    1.089±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3-甲基-1-丁烯 、 alkaline earth salt of/the/ methylsulfuric acid 在 cobalt(II) chloride 双氧水 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 130.0 ℃ 、1.5 MPa 条件下, 反应 8.0h, 生成 4-isopropyl-1,3-dioxolan-2-one
    参考文献:
    名称:
    摘要:
    Cyclic organic carbonates were prepared from epoxides (derivatives of C-3-C-16 olefins, C-4 and C-8 dienes, styrene; epichlorohydrin) in the presence of a catalytic system consisting of CoCl2 . 6H(2)O and dimethylformamide.
    DOI:
    10.1023/a:1026054529816
点击查看最新优质反应信息

文献信息

  • [EN] RESPIRATORY SYNCYTIAL VIRUS INHIBITORS<br/>[FR] INHIBITEURS DU VIRUS RESPIRATOIRE SYNCYTIAL
    申请人:MEDIVIR AB
    公开号:WO2017018924A1
    公开(公告)日:2017-02-02
    Compounds of Formula (I): (Formula I), wherein Z1 is NR1A, CHR1A or CR1BR1B; one of Z2 and Z3 is CH or CR1A', the other is N, CH or CR1A'; n is 0, 1 or 2; q is 0, 1 or 2; R1A, R1A', R1B, R2 and R3 are as defined herein, their use as inhibitors of RSV and related aspects.
    式(I)的化合物:(化学式I),其中Z1为NR1A,CHR1A或CR1BR1B;Z2和Z3中的一个为CH或CR1A',另一个为N,CH或CR1A';n为0、1或2;q为0、1或2;R1A、R1A'、R1B、R2和R3如本文所定义,它们作为RSV抑制剂及相关方面的用途。
  • One-Pot Synthesis of Cyclic Carbonates from Aldehydes, Sulfur Ylide, and CO2
    作者:Arumugam Sudalai、Ravindra Aher、B. Kumar
    DOI:10.1055/s-0033-1340072
    日期:——
    CH2=SMe2), in the presence of CO2 (1 atm) bubbled sequentially under mild conditions, produces cyclic carbonates in preparative yields. Sodium iodide formed in situ promotes the reaction between epoxide as intermediate and CO2 at ambient conditions, thus constituting a powerful metal-free synthesis of organic cyclic carbonates directly from aldehydes.
    在温和条件下连续鼓泡的 CO2 (1 atm) 存在下,用硫叶立德(CH2=SOMe2 或 CH2=SMe2)处理醛,以制备收率生成环状碳酸酯。在环境条件下,原位形成的碘化钠促进了作为中间体的环氧化物与 CO2 之间的反应,从而构成了直接由醛类强有力的无金属有机环状碳酸酯合成。
  • PRODRUGS OF FUSED HETEROCYCLIC INHIBITORS OF D-AMINO ACID OXIDASE
    申请人:Heffernan Michele L. R.
    公开号:US20110034434A1
    公开(公告)日:2011-02-10
    The invention relates to prodrugs of fused heterocyclic inhibitors of D-amino oxidase (DAAO) and methods of treating diseases and conditions, wherein modulation of D-amino acid oxidase activity, D-serine levels, D-serine oxidative products and NMDA receptor activity in the nervous system of a mammalian subject is effective.
    该发明涉及融合杂环抑制剂的前药,用于治疗疾病和病况的方法,其中在哺乳动物主体的神经系统中调节D-氨基酸氧化酶活性、D-丝氨酸水平、D-丝氨酸氧化产物和NMDA受体活性是有效的。
  • FUNCTIONALIZED FLUOROPOLYMERS AND ELECTROLYTE COMPOSITIONS
    申请人:Blue Current, Inc.
    公开号:US20160221926A1
    公开(公告)日:2016-08-04
    Provided herein are functionally substituted fluoropolymers suitable for use in liquid and solid non-flammable electrolyte compositions. The functionally substituted fluoropolymers include perfluoropolyethers (PFPEs) having high ionic conductivity. Also provided are non-flammable electrolyte compositions including functionally substituted PFPEs and alkali-metal ion batteries including the non-flammable electrolyte compositions.
    本文提供了功能性取代的氟聚合物,适用于液体和固体的无火电解质组成。这些功能性取代的氟聚合物包括具有高离子导电性的全氟聚醚(PFPEs)。还提供了包括功能性取代的PFPEs的无火电解质组成和碱金属离子电池,其中包括了这种无火电解质组成。
  • Flufenamic Acid-Promoted the Coupling of Epoxides and CO2 to Form Cyclic Carbonates
    作者:Ling Wu、Qingpeng Zeng、Pinghua Hu、Taoqi Zong、Fengtian Wu
    DOI:10.2174/1570178617999201110115648
    日期:2021.10
    <p>The process of hydrogen bond donor accelerating the cycloaddition of epoxides with CO2 is a green conversion. In this text, commercial drug flufenamic acid which contains O-H and N-H groups is introduced to promote the coupling. The reaction is capable of tolerating a relatively wide range of groups with the aid of catalytic system flufenamic acid/TBAB. Moreover, the reaction mechanism is proposed on the basis of reported literatures.</p> </sec></div> <div class="value-text ch">氢键供体促进环氧物与CO2的环加成反应是一种绿色转化过程。本文介绍了含有O-H和N-H基团的商业药物氟芬酸,用于促进偶联反应。在氟芬酸/TBAB催化体系的帮助下,该反应能够容忍相对较宽的基团范围。此外,根据已报告的文献提出了反应机理。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=310192br43883e6a48M0&inchikey=JOZQZYKBYAUYOK-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_1652" class="compound-item" title="顺式-4-[(甲基氨基甲酰)氨基]环己烷羧酸">顺式-4-[(甲基氨基甲酰)氨基]环己烷羧酸</a> <a target="_blank" href="https://www.molaid.com/MS_1695" class="compound-item" title="顺式-3-己烯醇碳酸甲酯">顺式-3-己烯醇碳酸甲酯</a> <a target="_blank" href="https://www.molaid.com/MS_3922" class="compound-item" title="镏碳酸盐二水">镏碳酸盐二水</a> <a target="_blank" 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" 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