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4-methyl-3-oxopentanamide | 34126-90-4

中文名称
——
中文别名
——
英文名称
4-methyl-3-oxopentanamide
英文别名
Isobutyroyl-acetamide;dimethylacetoacetamide
4-methyl-3-oxopentanamide化学式
CAS
34126-90-4
化学式
C6H11NO2
mdl
MFCD19206463
分子量
129.159
InChiKey
ZXFMVRLBIFNWKL-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

  • 熔点:
    68 °C
  • 沸点:
    105-107 °C(Press: 14 Torr)
  • 密度:
    1.026±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    60.2
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-methyl-3-oxopentanamide 作用下, 以 xylene 为溶剂, 生成 3-Amino-4-methyl-2-pentenamide
    参考文献:
    名称:
    Sato, Masayuki; Ogasawara, Hiromichi; Komatsu, Sachiko, Chemical and pharmaceutical bulletin, 1984, vol. 32, # 10, p. 3848 - 3856
    摘要:
    DOI:
  • 作为产物:
    描述:
    3-Amino-4-methyl-2-pentenamide盐酸 作用下, 以 氯仿 为溶剂, 反应 0.17h, 以87%的产率得到4-methyl-3-oxopentanamide
    参考文献:
    名称:
    Sato, Masayuki; Ogasawara, Hiromichi; Komatsu, Sachiko, Chemical and pharmaceutical bulletin, 1984, vol. 32, # 10, p. 3848 - 3856
    摘要:
    DOI:
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文献信息

  • Fe(III) Complex Compounds For The Treatment And Prophylaxis Of Iron Deficiency Symptoms And Iron Deficiency Anemias
    申请人:Bark Thomas
    公开号:US20130109662A1
    公开(公告)日:2013-05-02
    The invention relates to iron(III) complex compounds and pharmaceutical compositions comprising them for the use as medicaments, in particular for the treatment and/or prophylaxis of iron deficiency symptoms and iron deficiency anemias.
    这项发明涉及铁(III)配合物和包括它们的药物组合物,用作药物,特别是用于治疗和/或预防缺铁症状和缺铁性贫血。
  • [EN] POLYMERS PREPARED FROM MEVALONOLACTONE AND DERIVATIVES<br/>[FR] POLYMÈRES PRÉPARÉS À PARTIR DE LA MÉVALONOLACTONE ET DE SES DÉRIVÉS
    申请人:VISOLIS INC
    公开号:WO2016077555A1
    公开(公告)日:2016-05-19
    Described herein polymer precursor compounds (aka polymer building blocks) of derived from biobased compounds, and specifically biobased mevalonolactone and its related derivatives. Through oxidation these biobased precursors can be reacted to yield building blocks for (unsaturated-) polyesters, polyester polyols and polyamides, as well as precursors for glycidyl esters and omega-alkenyl esters. Through reduction, these biobased precursors can be reacted to yield building blocks for (unsaturated-) polyesters, polyester polyols, polycarbonates, as well as precursors for glycidyl ethers and omega-alkenyl ethers. Through nucleophilic ring opening and/or amidation, these biobased precursors can be reacted to yield building blocks for polyester polyols, chain-extender for polyurethanes, or polyester-amides.
    本文描述了从生物基化合物中衍生的聚合物前体化合物(又称聚合物构建模块),特别是生物基美伐酮内酯及其相关衍生物。通过氧化,这些生物基前体可以被反应生成(不饱和的)聚酯、聚酯多元醇和聚酰胺的构建模块,以及环氧酯和ω-烯基酯的前体。通过还原,这些生物基前体可以被反应生成(不饱和的)聚酯、聚酯多元醇、聚碳酸酯的构建模块,以及环氧醚和ω-烯基醚的前体。通过亲核环开和/或酰胺化,这些生物基前体可以被反应生成聚酯多元醇的构建模块,聚氨酯的扩链剂,或聚酯酰胺。
  • [EN] QUINAZOLINE DERIVATIVES<br/>[FR] DERIVES DE QUINAZOLINE
    申请人:ASTRAZENECA AB
    公开号:WO2005075439A1
    公开(公告)日:2005-08-18
    A quinazoline derivative of the formula (I) wherein: R1, R2, R3, R3a, R4, R5, R5a R6, R7, a, m and p are as defined in the description. Also claimed are pharmaceutical compositions containing the quinazoline derivative, the use of the quinazoline derivatives as medicaments and processes for the preparation of the quinazoline derivative. The quinazoline derivatives of formula (I), are useful in the treatment of hyperproliferative disorders such as a cancer.
    一种式(I)的喹唑啉衍生物,其中:R1、R2、R3、R3a、R4、R5、R5a、R6、R7、a、m和p如描述中所定义。还声明含有该喹唑啉衍生物的药物组合物,以及将该喹唑啉衍生物用作药物和制备该喹唑啉衍生物的方法。式(I)的喹唑啉衍生物在治疗高增殖性疾病如癌症方面具有用途。
  • POLYMERS PREPARED FROM MEVALONOLACTONE AND DERIVATIVES
    申请人:Visolis, Inc.
    公开号:US20160130389A1
    公开(公告)日:2016-05-12
    Described herein polymer precursor compounds (aka polymer building blocks) of derived from biobased compounds, and specifically biobased mevalonolactone and its related derivatives. Through oxidation these biobased precursors can be reacted to yield building blocks for (unsaturated-) polyesters, polyester polyols and polyamides, as well as precursors for glycidyl esters and omega-alkenyl esters. Through reduction, these biobased precursors can be reacted to yield building blocks for (unsaturated-) polyesters, polyester polyols, polycarbonates, as well as precursors for glycidyl ethers and omega-alkenyl ethers. Through nucleophilic ring opening and/or amidation, these biobased precursors can be reacted to yield building blocks for polyester polyols, chain-extender for polyurethanes, or polyester-amides.
    本文描述了从生物基化合物中衍生出的聚合物前体化合物(又称聚合物构建块),特别是生物基美瓦酮内酯及其相关衍生物。通过氧化,这些生物基前体可以反应产生(不饱和)聚酯、聚酯多元醇和聚酰胺的构建块,以及环氧酯和ω-烯基酯的前体。通过还原,这些生物基前体可以反应产生(不饱和)聚酯、聚酯多元醇、聚碳酸酯的构建块,以及环氧醚和ω-烯基醚的前体。通过亲核环开和/或酰胺化,这些生物基前体可以反应产生聚酯多元醇、聚氨酯的链延长剂,或聚酯酰胺的构建块。
  • 具有JAK激酶抑制活性化合物、制备方法、组 合物及用途
    申请人:北京鑫开元医药科技有限公司
    公开号:CN111303163B
    公开(公告)日:2020-08-11
    本发明属于药物领域,尤其涉及具有JAK激酶抑制活性化合物、制备方法、组合物及用途,所述化合物是具有式Ⅰ结构的化合物或其药学上可接受的盐:;式中,R1代表氢、羰基、取代或不取代的C1‑C5烷基;R2代表取代或不取代的C1‑C6烷基、取代或不取代的C1‑C6烷基羰基。本发明提供的化合物具有较好的JAK激酶抑制活性,可用于开发治疗肿瘤的药品,并具有特异性高、副作用低的优点。
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