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7-(1,1-二甲基乙基)-螺[3.5]-1,3-壬二酮 | 571152-35-7

中文名称
7-(1,1-二甲基乙基)-螺[3.5]-1,3-壬二酮
中文别名
——
英文名称
7-tert-butylspiro[3.5]nonane-1,3-dione
英文别名
Spiro[3.5]nonane-1,3-dione, 7-(1,1-dimethylethyl)-
7-(1,1-二甲基乙基)-螺[3.5]-1,3-壬二酮化学式
CAS
571152-35-7
化学式
C13H20O2
mdl
——
分子量
208.301
InChiKey
OGSPSUDMMYJEPD-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):
    3.3
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    N-isonicotinoyl-(L)-4-aminophenylalanine7-(1,1-二甲基乙基)-螺[3.5]-1,3-壬二酮四氢呋喃 为溶剂, 以86%的产率得到(S)-2-(7-tert-Butyl-3-oxo-spiro[3.5]non-1-en-1-ylamino)-3-{4-[(3,5-dichloro-pyridine-4-carbonyl)-amino]-phenyl}-propionic acid ethyl ester
    参考文献:
    名称:
    Efficient Synthesis of 3-Aminocyclobut-2-en-1-ones:  Squaramide Surrogates as Potent VLA-4 Antagonists
    摘要:
    [GRAPHICS]A novel series of uniquely functionalized 3-aminocyclobut-2-en-1-ones has been prepared by facile condensation of a variety of cyclobuta-1,3-diones with a phenylalanine-derived primary amine. These systems subsequently lend themselves to substitution at C-2 by reaction with a variety of electrophilic reagents including N-halosuccinimides, sulfenyl chlorides, and Eschenmoser's salt. Compounds from this novel series are potent antagonists of VLA-4.
    DOI:
    10.1021/ol034701n
  • 作为产物:
    描述:
    参考文献:
    名称:
    Efficient Synthesis of 3-Aminocyclobut-2-en-1-ones:  Squaramide Surrogates as Potent VLA-4 Antagonists
    摘要:
    [GRAPHICS]A novel series of uniquely functionalized 3-aminocyclobut-2-en-1-ones has been prepared by facile condensation of a variety of cyclobuta-1,3-diones with a phenylalanine-derived primary amine. These systems subsequently lend themselves to substitution at C-2 by reaction with a variety of electrophilic reagents including N-halosuccinimides, sulfenyl chlorides, and Eschenmoser's salt. Compounds from this novel series are potent antagonists of VLA-4.
    DOI:
    10.1021/ol034701n
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