摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(2-oxo-2-phenylethyl)-4-phenyl-1,2,4-triazolidine-3,5-dione | 98186-11-9

中文名称
——
中文别名
——
英文名称
1-(2-oxo-2-phenylethyl)-4-phenyl-1,2,4-triazolidine-3,5-dione
英文别名
1-Phenacyl-4-phenyl-1,2,4-triazolidine-3,5-dione
1-(2-oxo-2-phenylethyl)-4-phenyl-1,2,4-triazolidine-3,5-dione化学式
CAS
98186-11-9
化学式
C16H13N3O3
mdl
——
分子量
295.298
InChiKey
LMKIRZZXXPNYTA-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:
    130-133 °C
  • 密度:
    1.335±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    69.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-苯基-1,2,4-三唑啉-3,5-二酮苯乙酮三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以57%的产率得到1-(2-oxo-2-phenylethyl)-4-phenyl-1,2,4-triazolidine-3,5-dione
    参考文献:
    名称:
    Addition of 4-phenyltriazolinedione to carbonyl compounds: the formation of .alpha.-urazolyl carbonyl compounds
    摘要:
    DOI:
    10.1021/jo00288a032
点击查看最新优质反应信息

文献信息

  • Moriarty, Robert M.; Prakash, Indra, Synthetic Communications, 1985, vol. 15, # 7, p. 649 - 656
    作者:Moriarty, Robert M.、Prakash, Indra
    DOI:——
    日期:——
  • Synthesis and Cytotoxic Action of 1-Oxoalkyl and 1,2-Dioxoalkyl-1,2,4-triazolidine-3,5-diones in Murine and Human Tissue Cultured Cells
    作者:Christopher MacLauchlin、Iris H. Hall、Robert A. Izydore
    DOI:10.1002/(sici)1521-4184(19997)332:7<225::aid-ardp225>3.0.co;2-2
    日期:1999.7
    1-Oxoalkyl and 1,2-dioxoalkyl-1,2,4-triazolidine-3,5-diones proved to be potent antineoplastic agents in mouse tumors and potent cytotoxic agents particularly against the growth of suspended tumor cells. The compounds with shorter substituents in position 1 or positions 1 and 2 afforded the better activity. In L1210 lymphoid leukemia cells DNA, RNA, and protein syntheses were inhibited at 100 microM after 60 min. Multiple enzyme sites in nucleic acid metabolism were affected by the compounds, i.e. DNA polymerase alpha, PRPP-amido transferase, dihydrofolate reductase, thymidylate synthetase, and nucleoside kinases. These effects of the agents are probably additive in bringing about inhibition of DNA synthesis and cell death.
  • WILSON, R. MARSHALL;HENGGE, ALVAN C.;ATAEI, ALI;CHANTARASIRI, NUANPHUN, J. ORG. CHEM., 55,(1990) N, C. 193-197
    作者:WILSON, R. MARSHALL、HENGGE, ALVAN C.、ATAEI, ALI、CHANTARASIRI, NUANPHUN
    DOI:——
    日期:——
  • MORIARTY, R. M.;PRAKASH, INDRA, SYNTH. COMMUN., 1985, 15, N 7, 649-655
    作者:MORIARTY, R. M.、PRAKASH, INDRA
    DOI:——
    日期:——
查看更多