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o-Amino-ω-nitroacetophenon | 63892-06-8

中文名称
——
中文别名
——
英文名称
o-Amino-ω-nitroacetophenon
英文别名
ω-Nitro-o-amino-acetophenon;ω-nitro-o-amino-acetophenone;2'-amino-2-nitroacetophenone;2-aminophenyl nitromethylketone;1-(2-Aminophenyl)-2-nitroethanone
o-Amino-ω-nitroacetophenon化学式
CAS
63892-06-8
化学式
C8H8N2O3
mdl
——
分子量
180.163
InChiKey
BCAHFOPUWFFFOA-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):
    1.6
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    88.9
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • 1H-IMIDAZOPYRIDINE DERIVATIVES
    申请人:HOKURIKU SEIYAKU CO., LTD.
    公开号:EP1256582A1
    公开(公告)日:2002-11-13
    A 1H-imidazopyridine derivative represented by the following general formula (I) or a salt thereof having an inhibitory action against production of a cytokine: wherein R1 represents hydrogen atom, an alkyl group, a cycloalkyl group, or an aryl group; R2 represents a cycloalkyl group, an alkyl group, an aryl group, cyano group, mercapto group, carboxyl group, or carbamoyl group; ring A represents a homocyclic or heterocyclic ring; R3 represents an amino group or a saturated nitrogen-containing heterocyclic group; and k represents an integer of from 0 to 3; provided that the compound wherein R3 represents a saturated nitrogen-containing heterocyclic group and R2 is a non-substituted alkyl group is excluded.
    以下是通用公式(I)所代表的1H-咪唑吡啶衍生物或其对细胞因子产生抑制作用的盐,其中R1代表氢原子、烷基、环烷基或芳基;R2代表环烷基、烷基、芳基、基、巯基、羧基或基甲酰基;环A代表同环或异环;R3代表基或饱和氮杂环基;k代表0到3的整数;但其中R3代表饱和氮杂环基且R2为非取代烷基的化合物被排除在外。
  • New Indigo Syntheses. Preliminary Communication
    作者:Jacques Gosteli
    DOI:10.1002/hlca.19770600619
    日期:1977.9.21
    Three novel routes for the preparation of the dyestuff indigo are described. Two of the methods use isatoic anhydride, the third one styrene as starting materials. Key reactions are acylation of both dimsyl and nitromethane anions, Pummerer rearrangement and Nef reaction. A novel nitration of styrene is the basis of the third method.
    描述了三种制备靛蓝染料的新颖途径。两种方法均使用异戊酸酐,第三种方法使用苯乙烯作为起始原料。关键反应是二甲基和硝基甲烷阴离子的酰化,Pummerer重排和Nef反应。苯乙烯的新型硝化是第三种方法的基础。
  • 1h-imidazopyridine derivatives
    申请人:——
    公开号:US20040054182A1
    公开(公告)日:2004-03-18
    A 1H-imidazopyridine derivative represented by the following general formula (I) or a salt thereof having an inhibitory action against production of a cytokine: 1 wherein R 1 represents hydrogen atom, an alkyl group, a cycloalkyl group, or an aryl group; R 2 represents a cycloalkyl group, an alkyl group, an aryl group, cyano group, mercapto group, carboxyl group, or carbamoyl group; ring A represents a homocyclic or heterocyclic ring; R 3 represents an amino group or a saturated nitrogen-containing heterocyclic group; and k represents an integer of from 0 to 3; provided that the compound wherein R 3 represents a saturated nitrogen-containing heterocyclic group and R 2 is a non-substituted alkyl group is excluded.
    以下是一种1H-咪唑吡啶衍生物,其化学式如下(I),或其盐,具有抑制细胞因子产生的作用: 其中,R1代表氢原子、烷基、环烷基或芳基;R2代表环烷基、烷基、芳基、基、巯基、羧基或基甲酰基;环A代表同环或异环;R3代表基或饱和含氮杂环基;k表示0到3的整数;但其中R3代表饱和含氮杂环基,且R2为非取代烷基的化合物被排除在外。
  • US4117137A
    申请人:——
    公开号:US4117137A
    公开(公告)日:1978-09-26
  • US4151170A
    申请人:——
    公开号:US4151170A
    公开(公告)日:1979-04-24
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