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1-(2-methoxyphenyl)-3-oxopropan-1-one | 67860-32-6

中文名称
——
中文别名
——
英文名称
1-(2-methoxyphenyl)-3-oxopropan-1-one
英文别名
ω-Formyl-o-methoxyacetophenon;3-(2-Methoxyphenyl)-3-oxopropanal
1-(2-methoxyphenyl)-3-oxopropan-1-one化学式
CAS
67860-32-6
化学式
C10H10O3
mdl
——
分子量
178.188
InChiKey
PQWCBBHPJVEDMA-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:
    124-126 °C(Press: 17 Torr)
  • 密度:
    1.122±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:05ad72a8c171372c53547eb05a718ab8
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-(2-methoxyphenyl)-3-oxopropan-1-one三乙胺lithium chloride 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 12.5h, 生成 1-benzyl-4-(2-methoxy-phenyl)-6-oxo-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid tert-butylamide
    参考文献:
    名称:
    Highly Substituted Pyrrolidinones and Pyridones by 4-CR/2-CR Sequence
    摘要:
    By combining a Ugi four-component reaction of isocyanides, phosphonoacetic acids, primary amines, and glyoxals or alternatively 3-keto aldehydes with a subsequent Wittig ring-closing reaction (using the Horner/Wadsworth/Emmons variant (HWE)), highly substituted 5-oxo-2,5dihydro-1H-pyrrole-2-carboxylic acid amides and 6-oxo-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid amides can be assembled, respectively. The corresponding tandem of a Passerini reaction on 3-keto aldehydes and subsequent Wittig ring closure does not afford the expected six-membered 6-oxo-3,6-dihydro-2H-pyran-2-carboxylic acid amides but instead leads to the formation of 4-oxo-pent-2-enoic acid amides via an elimination route.
    DOI:
    10.1021/ol035787n
  • 作为产物:
    参考文献:
    名称:
    乙烯基异羟肟酸的合成,化学和生物学特性:5-脂氧合酶和IL-1生物合成的双重抑制剂。
    摘要:
    制备了乙烯基异羟肟酸(3-(N-羟基-N-烷基氨基)-2-丙烯-1-酮,VHA)作为抗炎剂。描述了这些相对未开发的化合物的合成,化学性质和体外生物学活性。通过将适当的N-取代的羟胺与以下三种试剂中的任何一种缩合来制备VHA:1,3-二羰基化合物(方法A);乙烯基酰胺(方法B);或炔烃(方法C)。VHA以一种或多种互变异构体的形式存在于溶液中,每种互变异构体的相对比例取决于VHA的结构,溶剂和pH。VHA会经历异羟肟酸和乙烯基酰胺类的某些典型反应。VHA在体外具有5-脂氧合酶和IL-1生物合成抑制剂的活性,不会抑制花生四烯酸级联反应的其他酶。ESR研究表明,它们可通过还原活性位点铁来抑制大豆1 15型脂氧合酶。
    DOI:
    10.1021/jm00100a011
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文献信息

  • Bi-functional complexes and methods for making and using such complexes
    申请人:Gouliaev Alex Haahr
    公开号:US11225655B2
    公开(公告)日:2022-01-18
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
    本发明涉及一种合成双功能复合物的方法,该复合物包括分子部分和识别分子部分的识别寡核苷酸部分。根据本发明的合成方法的一部分优选在一种或多种有机溶剂中进行,此时包含可选保护标签或寡核苷酸标识符的新生双功能复合物与固体支持物相连接,合成方法的另一部分优选在适合于将寡核苷酸标签酶加到溶液中的新生双功能复合物的条件下进行。
  • EIDEN F.; HERDEIS C.; FENNER H.; SCHIKORR W., ARCH. PHARM., 1978, 311, NO 6, 503-511
    作者:EIDEN F.、 HERDEIS C.、 FENNER H.、 SCHIKORR W.
    DOI:——
    日期:——
  • BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
    申请人:Nuevolution A/S
    公开号:EP2558577A1
    公开(公告)日:2013-02-20
  • BI-FUNCTINAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
    申请人:Gouliaev Alex Haahr
    公开号:US20130281324A1
    公开(公告)日:2013-10-24
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
  • [EN] BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES<br/>[FR] COMPLEXES BIFONCTIONNELS ET PROCÉDÉS DE FABRICATION ET D'UTILISATION DE TELS COMPLEXES
    申请人:NUEVOLUTION AS
    公开号:WO2011127933A1
    公开(公告)日:2011-10-20
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
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