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2-N,2-N-dibutyl-6-chloro-4-N-[4-[[4-chloro-6-(dibutylamino)-1,3,5-triazin-2-yl]amino]phenyl]-1,3,5-triazine-2,4-diamine | 33193-12-3

中文名称
——
中文别名
——
英文名称
2-N,2-N-dibutyl-6-chloro-4-N-[4-[[4-chloro-6-(dibutylamino)-1,3,5-triazin-2-yl]amino]phenyl]-1,3,5-triazine-2,4-diamine
英文别名
——
2-N,2-N-dibutyl-6-chloro-4-N-[4-[[4-chloro-6-(dibutylamino)-1,3,5-triazin-2-yl]amino]phenyl]-1,3,5-triazine-2,4-diamine化学式
CAS
33193-12-3
化学式
C28H42Cl2N10
mdl
——
分子量
589.614
InChiKey
DNANHFGDCJKUQW-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):
    9.6
  • 重原子数:
    40
  • 可旋转键数:
    18
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    108
  • 氢给体数:
    2
  • 氢受体数:
    10

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

  • 作为产物:
    描述:
    二正丁胺 在 cesium fluoride 作用下, 以 四氢呋喃N-甲基吡咯烷酮 为溶剂, 反应 3.0h, 生成 N2-(4-aminophenyl)-N4,N4-dibutyl-6-chloro-1,3,5-triazine-2,4-diamine 、 2-N,2-N-dibutyl-6-chloro-4-N-[4-[[4-chloro-6-(dibutylamino)-1,3,5-triazin-2-yl]amino]phenyl]-1,3,5-triazine-2,4-diamine
    参考文献:
    名称:
    Synthesis of polyguanamines from 2-N,N-dibutylamino-4,6-dichloro-1,3,5-triazine with aromatic diamines
    摘要:
    Solution polycondensation of 2-N,N-dibutylamino-4,6-dichloro-1,3,5-triazine (BDCT) with various aromatic diamines, including 4,4'-oxydianiline (ODA), p-phenylenediamine (pPDA), m-phenylenediamine (mPDA), o-tolidine (oTh), 4,4'-(9-fluorenylidene)dianiline (BAFL), and 2,4-diamino-6-(N,N-dibutylamino)-1,3,5-triazine (DABT), was investigated. High molecular weight (>10,000) polyguanamines (PGs) were obtained via the polymerization of BDCT with ODA, pPDA, oTD, and BAFL at 150-180 C in N-methylpyrrolidone (NMP) for 6 h. The polymerizability with BDCT was determined on the basis of the molecular weights of the polymers and the chemical shifts of the NMR data as follows: ODA > oTD > BAFL > pPDA > mPDA >> DABT. PGs were obtained from the reaction of BDCT with ODA and mPDA in only 55-77% yield, which may be attributed to the formation of cyclic oligomers. All of the polymers showed high thermostability (5% weight-loss temperature in N-2 greater than 444 degrees C), and the polymers generated from reaction of BDCT with ODA, mPDA, and BAFL exhibited good solubility in tetrahydrofuran and polar aprotic solvents such as NMP. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.reactfunctpolym.2013.03.005
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文献信息

  • Synthesis of polyguanamines from 2-N,N-dibutylamino-4,6-dichloro-1,3,5-triazine with aromatic diamines
    作者:Kyohei Saito、Naoya Nishimura、Shigeko Sasaki、Yoshiyuki Oishi、Yuji Shibasaki
    DOI:10.1016/j.reactfunctpolym.2013.03.005
    日期:2013.5
    Solution polycondensation of 2-N,N-dibutylamino-4,6-dichloro-1,3,5-triazine (BDCT) with various aromatic diamines, including 4,4'-oxydianiline (ODA), p-phenylenediamine (pPDA), m-phenylenediamine (mPDA), o-tolidine (oTh), 4,4'-(9-fluorenylidene)dianiline (BAFL), and 2,4-diamino-6-(N,N-dibutylamino)-1,3,5-triazine (DABT), was investigated. High molecular weight (>10,000) polyguanamines (PGs) were obtained via the polymerization of BDCT with ODA, pPDA, oTD, and BAFL at 150-180 C in N-methylpyrrolidone (NMP) for 6 h. The polymerizability with BDCT was determined on the basis of the molecular weights of the polymers and the chemical shifts of the NMR data as follows: ODA > oTD > BAFL > pPDA > mPDA >> DABT. PGs were obtained from the reaction of BDCT with ODA and mPDA in only 55-77% yield, which may be attributed to the formation of cyclic oligomers. All of the polymers showed high thermostability (5% weight-loss temperature in N-2 greater than 444 degrees C), and the polymers generated from reaction of BDCT with ODA, mPDA, and BAFL exhibited good solubility in tetrahydrofuran and polar aprotic solvents such as NMP. (C) 2013 Elsevier Ltd. All rights reserved.
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