摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5-(methylamino)-2-nitrophenol | 14703-78-7

中文名称
——
中文别名
——
英文名称
5-(methylamino)-2-nitrophenol
英文别名
2-nitro 5-N-methylamino phenol;2-Hydroxy-4-methylamino-1-nitro-benzol
5-(methylamino)-2-nitrophenol化学式
CAS
14703-78-7
化学式
C7H8N2O3
mdl
——
分子量
168.152
InChiKey
VEDQAJNCTODWDG-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):
    1.8
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    78.1
  • 氢给体数:
    2
  • 氢受体数:
    4

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
  • 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:
    5-(methylamino)-2-nitrophenolplatinum(IV) oxide氢气 作用下, 以 甲醇 为溶剂, 反应 15.0h, 生成 2-amino-5-(methylamino)phenol
    参考文献:
    名称:
    2-Aminobenzoxazole ligands of the hepatitis C virus internal ribosome entry site
    摘要:
    2-Aminobenzoxazoles have been synthesized as ligands for the hepatitis C virus (HCV) internal ribosome entry site (IRES) RNA. The compounds were designed to explore the less basic benzoxazole system as a replacement for the core scaffold in previously discovered benzimidazole viral translation inhibitors. Structure-activity relationships in the target binding of substituted benzoxazole ligands were investigated. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.05.088
  • 作为产物:
    描述:
    5-氟-2-硝基苯酚盐酸甲胺三乙胺 作用下, 以 乙腈 为溶剂, 反应 4.0h, 以89%的产率得到5-(methylamino)-2-nitrophenol
    参考文献:
    名称:
    2-Aminobenzoxazole ligands of the hepatitis C virus internal ribosome entry site
    摘要:
    2-Aminobenzoxazoles have been synthesized as ligands for the hepatitis C virus (HCV) internal ribosome entry site (IRES) RNA. The compounds were designed to explore the less basic benzoxazole system as a replacement for the core scaffold in previously discovered benzimidazole viral translation inhibitors. Structure-activity relationships in the target binding of substituted benzoxazole ligands were investigated. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.05.088
点击查看最新优质反应信息

文献信息

  • Hair dye compositions and new compounds useful therein
    申请人:Societe Anonyme dite: L'OREAL
    公开号:US04337061A1
    公开(公告)日:1982-06-29
    Novel compounds of the general formula ##STR1## wherein Z represents a substituted lower alkyl radical; each of R.sub.1 and R.sub.2 is hydrogen atom, a lower alkyl or a substituted lower alkyl identical with or different from Z and the functional groups NO.sub.2 and NR.sub.1 R.sub.2 can occupy all ring positions in relation to OZ, with the exception that if Z is .beta.-hydroxyethyl, --NO.sub.2 is in the 4 position and --N(R.sub.1)(R.sub.2) is in the 2 position then either R.sub.1 or R.sub.2 is other than hydrogen. The novel compounds are for dyeing human hair in a variety of yellow shades. The compounds of formula (I) may be used as aqueous or water-alcohol solutions to form dye compositions for dyeing human hair.
    通用公式##STR1##中的新化合物,其中Z代表取代的较低烷基基团;R.sub.1和R.sub.2中的每一个是氢原子、较低烷基或与Z相同或不同的取代较低烷基,功能基团NO.sub.2和NR.sub.1 R.sub.2可以占据相对于OZ的所有环位置,但如果Z为β-羟乙基,则--NO.sub.2位于4位,--N(R.sub.1)(R.sub.2)位于2位,则R.sub.1或R.sub.2中的一个不是氢。这些新化合物用于染色人类头发,产生各种黄色调。公式(I)的化合物可用作水性或水醇溶液,用于制备染色人类头发的染料组合物。
  • POLY(OXYALKYLENE) HYDROXY AND AMINO AROMATIC CARBAMATES AND FUEL COMPOSITIONS CONTAINING THE SAME
    申请人:Chevron Chemical Company LLC
    公开号:EP0706554B1
    公开(公告)日:2000-06-07
  • POLYALKYL HYDROXY AND AMINO AROMATIC CARBAMATES AND FUEL COMPOSITIONS CONTAINING THE SAME
    申请人:CHEVRON CHEMICAL COMPANY
    公开号:EP0706551A1
    公开(公告)日:1996-04-17
  • EP0706551A4
    申请人:——
    公开号:EP0706551A4
    公开(公告)日:1996-09-18
  • EP0706554A4
    申请人:——
    公开号:EP0706554A4
    公开(公告)日:1996-09-18
查看更多