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tert-butyl 1-oxo-1,2-dihydrospiro(benzo[f]chromene-3,4'-piperidine)-1'-carboxylate | 1013333-60-2

中文名称
——
中文别名
——
英文名称
tert-butyl 1-oxo-1,2-dihydrospiro(benzo[f]chromene-3,4'-piperidine)-1'-carboxylate
英文别名
1,1-Dimethylethyl 1,2-dihydro-1-oxospiro[3H-naphtho[2,1-b]pyran-3,4a(2)-piperidine]-1a(2)-carboxylate;tert-butyl 1-oxospiro[2H-benzo[f]chromene-3,4'-piperidine]-1'-carboxylate
tert-butyl 1-oxo-1,2-dihydrospiro(benzo[f]chromene-3,4'-piperidine)-1'-carboxylate化学式
CAS
1013333-60-2
化学式
C22H25NO4
mdl
——
分子量
367.445
InChiKey
YHBKMAXUQLEZNF-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:
    536.1±50.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    55.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-乙酰基-2-萘酚N-叔丁氧羰基-4-哌啶酮四氢吡咯 作用下, 反应 0.15h, 以90%的产率得到tert-butyl 1-oxo-1,2-dihydrospiro(benzo[f]chromene-3,4'-piperidine)-1'-carboxylate
    参考文献:
    名称:
    Green synthesis of new naphthospiro chromanone scaffolds and their antimicrobial activity
    摘要:
    An efficient synthesis of new naphthospiro chromanone scaffolds using ionic liquids as a green solvent under microwave irradiation is presented. The reaction was also studied under conventional elevated temperature conditions. The structures of newly synthesized compounds have been elucidated by means of IR, H-1 NMR, C-13 NMR, and mass spectrometry data. All compounds were screened for their antimicrobial activity.
    DOI:
    10.1134/s1070363214080301
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文献信息

  • Green synthesis of new naphthospiro chromanone scaffolds and their antimicrobial activity
    作者:M. Sarasija、K. Sudershan、D. Ashok、Shivaraj
    DOI:10.1134/s1070363214080301
    日期:2014.8
    An efficient synthesis of new naphthospiro chromanone scaffolds using ionic liquids as a green solvent under microwave irradiation is presented. The reaction was also studied under conventional elevated temperature conditions. The structures of newly synthesized compounds have been elucidated by means of IR, H-1 NMR, C-13 NMR, and mass spectrometry data. All compounds were screened for their antimicrobial activity.
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