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1,6-diamino-2-methoxynaphthalene | 1392006-63-1

中文名称
——
中文别名
——
英文名称
1,6-diamino-2-methoxynaphthalene
英文别名
2-Methoxynaphthalene-1,6-diamine
1,6-diamino-2-methoxynaphthalene化学式
CAS
1392006-63-1
化学式
C11H12N2O
mdl
——
分子量
188.229
InChiKey
VZHQEWGGTGUQJI-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:
    406.6±30.0 °C(Predicted)
  • 密度:
    1.237±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    61.3
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    1,6-二溴-2-甲氧基萘 在 C24H12Cu2F9N4O7四丁基溴化铵caesium carbonate 作用下, 以 为溶剂, 反应 16.0h, 以100%的产率得到1,6-diamino-2-methoxynaphthalene
    参考文献:
    名称:
    Diamination of Phenylene Dihalides Catalyzed by a Dicopper Complex
    摘要:
    Diamination of phenylene dihalides with aqueous ammonia to give the corresponding phenylenediamines can be achieved by using a dicopper complex [Cu-2(bpnp)(OH)(CF3COO)(3)] (1) (bpnp = 2,7-bis(pyridine-2-yl)-1,8-naphthyridine) as the catalyst in the presence of Bu4NBr and Cs2CO3 in high yields. In addition, 1,3,5-tribromobenzene was converted into benzenetriamine quantitatively under the same conditions. This method offers a new opportunity, particularly simplifying steps and increasing yields, for the preparation of aryl diamines.
    DOI:
    10.1021/jo301244p
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文献信息

  • Diamination of Phenylene Dihalides Catalyzed by a Dicopper Complex
    作者:Bei-Sih Liao、Shiuh-Tzung Liu
    DOI:10.1021/jo301244p
    日期:2012.8.3
    Diamination of phenylene dihalides with aqueous ammonia to give the corresponding phenylenediamines can be achieved by using a dicopper complex [Cu-2(bpnp)(OH)(CF3COO)(3)] (1) (bpnp = 2,7-bis(pyridine-2-yl)-1,8-naphthyridine) as the catalyst in the presence of Bu4NBr and Cs2CO3 in high yields. In addition, 1,3,5-tribromobenzene was converted into benzenetriamine quantitatively under the same conditions. This method offers a new opportunity, particularly simplifying steps and increasing yields, for the preparation of aryl diamines.
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