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2,5-二甲氧基-2-甲基四氢呋喃 | 58518-63-1

中文名称
2,5-二甲氧基-2-甲基四氢呋喃
中文别名
——
英文名称
2,5-dimethoxy-2-methyl-tetrahydro-furan
英文别名
2-methyl-2,5-dimethoxy-tetrahydrofurane;2-methyl-2,5-dimethoxy-tetrahydrofuran;2,5-dimethoxy-2-methyltetrahydrofuran;2-Methyl-2,5-dimethoxytetrahydrofuran;2,5-dimethoxy-2-methyloxolane
2,5-二甲氧基-2-甲基四氢呋喃化学式
CAS
58518-63-1
化学式
C7H14O3
mdl
——
分子量
146.186
InChiKey
GZYGYLSHLHOMAO-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:
    69-70 °C(Press: 9 Torr)
  • 密度:
    1.00±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:508ec99561636705836efb7c15013cc1
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反应信息

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文献信息

  • Complete Regioselectivity in Staurosporine Chromophore Formation
    作者:Stefan Eils、Ekkehard Winterfeldt
    DOI:10.1055/s-1999-3383
    日期:1999.2
    For the preparation of regioselectively N-substituted indolocarbazole alkaloids two strategies have been employed: 1. the exploitation of different electronic situations at the nitrogen atoms, and 2, the utilization of an orthogonal protecting group strategy that allows regioselective glycoside formation.
    在制备区域选择性N取代的吲哚并咯嗪生物碱时,采用了两种策略:1. 利用氮原子上的不同电子环境;2. 采取正交保护基团策略,以实现区域选择性的糖苷形成。
  • 1H-QUINAZOLINE-2,4-DIONES
    申请人:NOVARTIS AG
    公开号:US20130296332A1
    公开(公告)日:2013-11-07
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及公式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范所定义,它们的制备,它们作为药物的用途,以及含有它们的药物组合物。此外,还公开了制造公式(I)化合物的中间体和包含公式(I)化合物的组合物。
  • 1H-Quinazoline-2,4-Diones
    申请人:Allgeier Hans
    公开号:US20080153836A1
    公开(公告)日:2008-06-26
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及公式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范中所定义,它们的制备,它们作为药物的用途以及含有它们的药物组合物。此外,还揭示了制造公式(I)化合物的中间体和包含公式(I)化合物的组合物。
  • Quinazoline Derivatives
    申请人:Allgeier Hans
    公开号:US20070208018A1
    公开(公告)日:2007-09-06
    The present invention relates to 1H-Quinazoline-2,4-dione derivatives of formula(I) wherein the substituents are defined as in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them.
    本发明涉及式(I)的1H-喹唑啉-2,4-二酮衍生物,其中取代基的定义如规范中所述,它们的制备方法,它们作为药物的用途,以及含有它们的药物组合物。
  • 1H-QUINAZ0LINE-2,4-DIONES
    申请人:ALLGEIER Hans
    公开号:US20100144747A1
    公开(公告)日:2010-06-10
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范中所定义,它们的制备,它们作为药物的用途以及包含它们的制药组合物。此外,还披露了制备式(I)化合物的中间体和包含式(I)化合物的组合物。
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