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2,4-Dimethyl-2-isopropyl-1,3-dioxolan | 25186-44-1

中文名称
——
中文别名
——
英文名称
2,4-Dimethyl-2-isopropyl-1,3-dioxolan
英文别名
2,4-Dimethyl-2-(1-methylethyl)-1,3-dioxolane;2,4-dimethyl-2-propan-2-yl-1,3-dioxolane
2,4-Dimethyl-2-isopropyl-1,3-dioxolan化学式
CAS
25186-44-1
化学式
C8H16O2
mdl
——
分子量
144.214
InChiKey
KYASJMMKTOPSEK-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:
    147.6±8.0 °C(Predicted)
  • 密度:
    0.893±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 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

  • 作为产物:
    描述:
    3-甲基-2-丁酮1,2-丙二醇 在 salicylic acid resin supported FeCl3 作用下, 以 为溶剂, 反应 2.0h, 以72.7%的产率得到2,4-Dimethyl-2-isopropyl-1,3-dioxolan
    参考文献:
    名称:
    Huirong, Yang; Yingde, Li Bina Cui, Synthetic Communications, 1998, vol. 28, # 7, p. 1233 - 1238
    摘要:
    DOI:
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文献信息

  • PRODUCTION OF CYCLIC ACETALS OR KETALS USING SOLID ACID CATALYSTS
    申请人:Terrill Daniel Latham
    公开号:US20120330032A1
    公开(公告)日:2012-12-27
    A process for making a cyclic compounds such as cyclic acetal or cyclic ketones by feeding aldehyde or ketone compounds and polyhydroxyl compounds to a reaction zone at a molar ratio of polyhydroxyl compounds to aldehyde or ketone compounds of at least 3:1, reacting these compounds in the presence of a solid acid such as an acidic ion exchange resin, to generate a liquid reaction mixture without separating water from the reaction mixture as it is being formed in the reaction mixture, withdrawing the liquid reaction mixture from the reaction zone as a liquid product stream, and feeding the liquid reaction product stream to a distillation column to separate cyclic acetal compounds from unreacted polyhydroxyl compounds, and optionally recycling back the unreacted polyhydroxyl compounds to the reaction zone. The process produces cyclic acetal compounds in yields of at least 90% with long catalyst life. The process is also suitable to make cyclic ketals from ketone compounds.
    通过将醛或酮化合物和多羟基化合物以多羟基化合物与醛或酮化合物的摩尔比至少为3:1的比例送入反应区域,在固体酸的存在下(如酸性离子交换树脂)中反应这些化合物,生成液体反应混合物而不将水从反应混合物中分离出来,将液体反应混合物从反应区域中作为液体产品流撤出,并将液体反应产物流送入蒸馏塔以从未反应的多羟基化合物中分离出环状缩醛化合物,并可选择性地将未反应的多羟基化合物回收到反应区域。该过程以至少90%的产率生产环状缩醛化合物,并具有长寿命的催化剂。该过程也适用于从酮化合物制备环状缩酮。
  • PRODUCTION OF CYCLIC ACETALS OR KETALS USING LIQUID-PHASE ACID CATALYSTS
    申请人:Terrill Daniel Latham
    公开号:US20120330033A1
    公开(公告)日:2012-12-27
    A process for making a cyclic compounds such as cyclic acetal or cyclic ketones by feeding aldehyde or ketone compounds and polyhydroxyl compounds to a reaction vessel at a molar ratio of polyhydroxyl compounds to aldehyde or ketone compounds of at least 3:1, reacting these compounds in the presence of a homogeneous acid catalyst to generate a liquid phase homogeneous reaction mixture containing the acid catalyst without separating water from the reaction mixture as it is being formed in the reaction mixture, withdrawing the liquid phase homogeneous reaction mixture from the reaction vessel as a liquid product stream, and feeding the liquid reaction product stream to a distillation column to separate cyclic acetal compounds from unreacted polyhydroxyl compounds, and optionally recycling back the unreacted polyhydroxyl compounds and/or acid catalyst to the reaction vessel. The process produces cyclic acetal compounds in high yields. The process is also suitable to make cyclic ketals from ketone compounds.
    通过将醛或酮化合物和多羟基化合物以多羟基化合物与醛或酮化合物的摩尔比至少为3:1的比例加入到反应容器中,通过在均相酸催化剂存在下反应这些化合物,生成含有酸催化剂的液相均相反应混合物,而不从反应混合物中分离水,将液相均相反应混合物从反应容器中作为液体产品流撤出,并将液体反应产物流送入蒸馏塔以将环状缩醛化合物与未反应的多羟基化合物分离,并可选择性地将未反应的多羟基化合物和/或酸催化剂回收到反应容器中。该过程以高产率生产环状缩醛化合物。该过程也适用于从酮化合物制备环状缩酮。
  • BIS-ARYL SULFONAMIDES
    申请人:Ungashe Solomon
    公开号:US20080261966A1
    公开(公告)日:2008-10-23
    Compounds are provided that act as potent antagonists of chemokine receptors. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of chemokine receptor-mediated diseases, and as controls in assays for the identification of chemokine antagonists.
    提供了化合物,可作为趋化因子受体的有效拮抗剂。这些化合物通常是芳基磺酰胺衍生物,可用于制备药物组合物,治疗趋化因子受体介导的疾病,并作为化学试剂中趋化因子拮抗剂的鉴定控制。
  • Aryl Sulfonamides
    申请人:Ungashe Solomon
    公开号:US20080161345A1
    公开(公告)日:2008-07-03
    The present invention relates to compounds that modulate various chemokine receptors. These compounds are useful for treating inflammatory and immune diseases.
    本发明涉及调节各种趋化因子受体的化合物。这些化合物可用于治疗炎症和免疫性疾病。
  • MESLARD, J. C.;SUBIRA, F.;VAIRON, J. P.;GUY, A.;GARREAU, R., BULL. SOC. CHIM. FR., 1985, N 1, 84-89
    作者:MESLARD, J. C.、SUBIRA, F.、VAIRON, J. P.、GUY, A.、GARREAU, R.
    DOI:——
    日期:——
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