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4-[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-benzoic acid

中文名称
——
中文别名
——
英文名称
4-[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-benzoic acid
英文别名
4-[(4,6-Dichloro-1,3,5-triazin-2-yl)oxy]benzoic acid;4-[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]benzoic acid
4-[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-benzoic acid化学式
CAS
——
化学式
C10H5Cl2N3O3
mdl
——
分子量
286.074
InChiKey
LBNXREXRJLSMIO-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:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    85.2
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    4-[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-benzoic acid聚甘氨酸 在 sodium hydroxide 作用下, 以 为溶剂, 反应 0.33h, 以76%的产率得到4-[[4,6-Bis(carboxymethylamino)-1,3,5-triazin-2-yl]oxy]benzoic acid
    参考文献:
    名称:
    Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
    摘要:
    A rapid and efficient method for preparation of C-2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C-2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2014.06.127
  • 作为产物:
    描述:
    三聚氯氰对羟基苯甲酸 在 sodium hydroxide 作用下, 以 丙酮 为溶剂, 反应 3.0h, 以82%的产率得到4-[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-benzoic acid
    参考文献:
    名称:
    Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
    摘要:
    A rapid and efficient method for preparation of C-2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C-2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2014.06.127
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文献信息

  • Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
    作者:Watcharee Funfuenha、Wong Phakhodee、Mookda Pattarawarapan
    DOI:10.1016/j.tet.2014.06.127
    日期:2014.9
    A rapid and efficient method for preparation of C-2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C-2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks. (C) 2014 Elsevier Ltd. All rights reserved.
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