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2-methyl-2-propoxypropionaldehyde

中文名称
——
中文别名
——
英文名称
2-methyl-2-propoxypropionaldehyde
英文别名
2-methyl-2-propoxypropanal
2-methyl-2-propoxypropionaldehyde化学式
CAS
——
化学式
C7H14O2
mdl
——
分子量
130.187
InChiKey
AMYWCLOUFDSHLP-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

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文献信息

  • MOLECULAR PRECURSOR COMPOUNDS FOR ZINC-GROUP 13 MIXED OXIDE MATERIALS
    申请人:Precursor Energetics, Inc.
    公开号:US20150218190A1
    公开(公告)日:2015-08-06
    Molecular precursor compounds, processes and compositions for making Zn-Group 13 mixed oxide materials including IZO, GZO, AZO and BZO, by providing inks comprising a molecular precursor compound having the formula M A a Zn(OROR) 3a+2 , and printing or depositing the inks on a substrate. The printed or deposited ink films can be treated to convert the molecular precursor compounds to a material.
    分子前体化合物、制备Zn-Group 13混合氧化物材料(包括IZO、GZO、AZO和BZO)的过程和组合物,方法是提供包含具有公式M的分子前体化合物的油墨,在基底上印刷或沉积这些油墨。印刷或沉积的油墨膜可以经处理转化为材料。
  • Compounds
    申请人:Tiden Anna-Karin
    公开号:US20080221133A1
    公开(公告)日:2008-09-11
    The present invention relates to a compound according to Formula (I) wherein R 1 is selected from C 1 -C 6 alkyl, and said C 1 -C 6 alkyl is substituted with C 1 -C 6 alkoxy; and at least one of said C 1 -C 6 alkyl or said C 1 -C 6 alkoxy is branched; or a pharmaceutically acceptable salt thereof, solvate or solvate of a salt thereof, as well as, to compositions containing at least one compound according to Formula (I) and methods of treating at least one disease or condition therewith.
    本发明涉及一种化合物,其化学式为(I)式,其中R1选自C1-C6烷基,所述C1-C6烷基被C1-C6烷氧基取代;且所述C1-C6烷基或所述C1-C6烷氧基中至少有一个是支链的;或其药学上可接受的盐、溶剂或其盐的溶剂,以及至少含有一种化合物(I)的组合物和使用该组合物治疗至少一种疾病或病况的方法。
  • 2-Thioxanthine Derivatives Acting as MPO-Inhibitors
    申请人:Tiden Anna-Karin
    公开号:US20090131459A1
    公开(公告)日:2009-05-21
    The present invention relates to a compound according to Formula (I) wherein R 1 is selected from C 1 -C 6 alkyl, and said C 1 -C 6 alkyl is substituted with C 1 -C 6 alkoxy; and at least one of said C 1 -C 6 alkyl or said C 1 -C 6 alkoxy is branched; or a pharmaceutically acceptable salt thereof, solvate or solvate of a salt thereof, to compositions containing the compound and the use thereof in therapy.
    本发明涉及一种化合物,其化学式为(I),其中R1选自C1-C6烷基,所述的C1-C6烷基被C1-C6烷氧基取代; 并且所述的C1-C6烷基或所述的C1-C6烷氧基中至少有一个是支链的; 或其药学上可接受的盐,溶剂或其盐的溶剂,以及包含该化合物的组合物和其在治疗中的用途。
  • 1,3-Dioxane ethers
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0201351A2
    公开(公告)日:1986-11-12
    The invention concerns novel 1,3-dioxane ethers of the formula I, wherein R1 includes alkyl, cycloalkyl, phenyl and phenylalkyl, R2 and R3 include hydrogen and alkyl, n is 1 or 2, m is 2, 3 or 4, p is zero, 1 or 2, and Z is carboxy or 1 (H)-tetrazol-5-yl, and pharmaceutically acceptable salts thereof, for use in conjunction with their pharmaceutical compositions in the treatment of certain pulmonary and/or vascular disorders. The invention also describes various processes and intermediates for the manufacture of the novel compounds.
    本发明涉及式 I 的新型 1,3-二氧六环醚,其中 R1 包括烷基、环烷基、苯基和苯基烷基,R2 和 R3 包括氢和烷基,n 为 1 或 2,m 为 2、3 或 4,p 为 0、1 或 2,Z 为羧基或 1 (H)-tetrazol-5-yl 及其药学上可接受的盐类,可与它们的药物组合物一起用于治疗某些肺部和/或血管疾病。 本发明还描述了制造这些新型化合物的各种工艺和中间体。
  • Therapeutic agents
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0266979A2
    公开(公告)日:1988-05-11
    The invention concerns novel therapeutic agents containing a (Z)-(2-alkoxyalkyl- or 2-aryloxyalkyl-4-phenyl-1,3-­dioxan-5-yl)alkenoic acid, or a related tetrazole derivative, which antagonises one or more of the actions of thromboxane A₂, together with a compound which inhibits the synthesis of thromboxane A₂. The compositions are useful as medicines in treating a variety of diseases or medical conditions in which thromboxane A₂ and/or other prostanoid contractile substances are involved.
    本发明涉及含有(Z)-(2-烷氧基烷基-或 2-芳氧基烷基-4-苯基-1,3-二氧杂环戊-5-基)烯酸或相关四唑衍生物的新型治疗剂,该治疗剂与抑制血栓素 A₂合成的化合物一起,可拮抗血栓素 A₂的一种或多种作用。 这些组合物可作为药物用于治疗涉及血栓素 A₂和/或其他类固醇收缩物质的多种疾病或病症。
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