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methyl 5-vinyl-2-naphthoate | 150256-04-5

中文名称
——
中文别名
——
英文名称
methyl 5-vinyl-2-naphthoate
英文别名
Methyl 5-ethenylnaphthalene-2-carboxylate
methyl 5-vinyl-2-naphthoate化学式
CAS
150256-04-5
化学式
C14H12O2
mdl
——
分子量
212.248
InChiKey
CBZLMABSDAJGEA-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:
    346.2±11.0 °C(Predicted)
  • 密度:
    1.132±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    methyl 5-vinyl-2-naphthoate二异丁基氢化铝 作用下, 以 四氢呋喃 为溶剂, 反应 18.0h, 生成 (5-Ethenylnaphthalen-2-yl)methanol
    参考文献:
    名称:
    Antihyperglycemic activity of novel naphthalenylmethyl-3H-1,2,3,5-oxathiadiazole 2-oxides
    摘要:
    A series of naphthalenyl 3H-1,2,3,5-oxathiadiazole 2-oxides was prepared and tested for antihyperglycemic activity in the db/db mouse, a model for type 2 (non-insulin dependent) diabetes mellitus. Substitution at the 1-, 5-, or 8-positions of the naphthalene ring with a halogen was found to be beneficial to antihyperglycemic activity. 4-[(5-Chloronaphthalen-2-yl)methyl]-3H-1,2,3,5-oxathiadiazole 2-oxide (45), one of the most potent compounds in this series, was selected for further pharmacological evaluation.
    DOI:
    10.1021/jm00069a006
  • 作为产物:
    描述:
    5-溴-2-萘甲酸甲酯三丁基乙烯基锡四(三苯基膦)钯 作用下, 以 甲苯 为溶剂, 反应 4.0h, 以73%的产率得到methyl 5-vinyl-2-naphthoate
    参考文献:
    名称:
    Antihyperglycemic activity of novel naphthalenylmethyl-3H-1,2,3,5-oxathiadiazole 2-oxides
    摘要:
    A series of naphthalenyl 3H-1,2,3,5-oxathiadiazole 2-oxides was prepared and tested for antihyperglycemic activity in the db/db mouse, a model for type 2 (non-insulin dependent) diabetes mellitus. Substitution at the 1-, 5-, or 8-positions of the naphthalene ring with a halogen was found to be beneficial to antihyperglycemic activity. 4-[(5-Chloronaphthalen-2-yl)methyl]-3H-1,2,3,5-oxathiadiazole 2-oxide (45), one of the most potent compounds in this series, was selected for further pharmacological evaluation.
    DOI:
    10.1021/jm00069a006
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