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N'-(4-羟基苯基)-N,N-二甲基-甲脒 | 2350-51-8

中文名称
N'-(4-羟基苯基)-N,N-二甲基-甲脒
中文别名
——
英文名称
N-(p-Hydroxyphenyl)-N',N'-dimethylformamidin
英文别名
Formamidine, N'-(p-hydroxyphenyl)-N,N-dimethyl-;N'-(4-hydroxyphenyl)-N,N-dimethylmethanimidamide
N'-(4-羟基苯基)-N,N-二甲基-甲脒化学式
CAS
2350-51-8
化学式
C9H12N2O
mdl
——
分子量
164.207
InChiKey
YXTSZBNGJXQOIM-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:
    210-215 °C

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    35.8
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S26,S36
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2925290090

SDS

SDS:1609bfa8be29d0c65e4ae3f12682729f
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上下游信息

  • 下游产品
    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:
    N'-(4-羟基苯基)-N,N-二甲基-甲脒3,4-二氯氯苄氢氧化钾 作用下, 以 二甲基亚砜 为溶剂, 生成 N'-[4-(3,4-Dichloro-benzyloxy)-phenyl]-N,N-dimethyl-formamidine
    参考文献:
    名称:
    CH563713
    摘要:
    公开号:
  • 作为产物:
    参考文献:
    名称:
    Annovel formamidine linker for use in solid-phase synthesis
    摘要:
    A variety of amidines have been evaluated as linkers for solid-supported synthesis. As a demonstration of its utility, an amidine linker was used to prepare a set of compounds involving amine exchange, oxidation, reduction and ether formation reactions. These compounds were successfully cleaved from the support to generate alpha-substituted, secondary amine derivatives, which were thoroughly characterized by spectroscopic methods. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(97)01200-8
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文献信息

  • CH563713
    申请人:——
    公开号:——
    公开(公告)日:——
  • Annovel formamidine linker for use in solid-phase synthesis
    作者:Paul S. Furth、Michael S. Reitman、Alan F. Cook
    DOI:10.1016/s0040-4039(97)01200-8
    日期:1997.8
    A variety of amidines have been evaluated as linkers for solid-supported synthesis. As a demonstration of its utility, an amidine linker was used to prepare a set of compounds involving amine exchange, oxidation, reduction and ether formation reactions. These compounds were successfully cleaved from the support to generate alpha-substituted, secondary amine derivatives, which were thoroughly characterized by spectroscopic methods. (C) 1997 Elsevier Science Ltd.
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