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4-chlorocarbonyl-2,6-dimethylmorpholine | 1601099-54-0

中文名称
——
中文别名
——
英文名称
4-chlorocarbonyl-2,6-dimethylmorpholine
英文别名
2,6-Dimethylmorpholine-4-carbonyl chloride
4-chlorocarbonyl-2,6-dimethylmorpholine化学式
CAS
1601099-54-0
化学式
C7H12ClNO2
mdl
——
分子量
177.631
InChiKey
ROBIABICEDEGND-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):
    1.3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-chlorocarbonyl-2,6-dimethylmorpholine一水合肼 作用下, 以 1,4-二氧六环N,N-二甲基甲酰胺 为溶剂, 反应 36.0h, 生成 2-(2,6-dimethylmorpholine-4-carbonyl)-N-(4-methoxy-3H-imidazo[4,5-c]pyridin-2-yl)hydrazine-1-carbothioamide
    参考文献:
    名称:
    [EN] IMIDAZOPYRIDINE AND OXAZOLOPYRIDINE DERIVATIVES AND ANALOGS THEREOF, METHODS OF PREPARATION THEREOF, METHODS OF HIF-1/2A PATHWAY INHIBITION, AND INDUCTION OF FERROPTOSIS
    [FR] DÉRIVÉS D'IMIDAZOPYRIDINE ET D'OXAZOLOPYRIDINE ET LEURS ANALOGUES, LEURS PROCÉDÉS DE PRÉPARATION, PROCÉDÉS D'INHIBITION DE LA VOIE HIF-1/2A ET INDUCTION DE LA FERROPTOSE
    摘要:
    Novel substituted imidazopyridine and oxazolopyridine compounds that are useful as inhibitors of HIF-1α and HIF-2α and inducers of ferroptosis through perturbations in iron metabolism, synthetic methods for making said compounds, pharmaceutical compositions comprising the compounds, and methods of using the compounds and compositions to treat disorders associated with dysfunction of HIF-1/2α or iron metabolism.
    公开号:
    WO2023234970A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    [EN] IMIDAZOPYRIDINE AND OXAZOLOPYRIDINE DERIVATIVES AND ANALOGS THEREOF, METHODS OF PREPARATION THEREOF, METHODS OF HIF-1/2A PATHWAY INHIBITION, AND INDUCTION OF FERROPTOSIS
    [FR] DÉRIVÉS D'IMIDAZOPYRIDINE ET D'OXAZOLOPYRIDINE ET LEURS ANALOGUES, LEURS PROCÉDÉS DE PRÉPARATION, PROCÉDÉS D'INHIBITION DE LA VOIE HIF-1/2A ET INDUCTION DE LA FERROPTOSE
    摘要:
    Novel substituted imidazopyridine and oxazolopyridine compounds that are useful as inhibitors of HIF-1α and HIF-2α and inducers of ferroptosis through perturbations in iron metabolism, synthetic methods for making said compounds, pharmaceutical compositions comprising the compounds, and methods of using the compounds and compositions to treat disorders associated with dysfunction of HIF-1/2α or iron metabolism.
    公开号:
    WO2023234970A1
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文献信息

  • Diacyl indazole derivatives as lipase and phospholipase inhibitors
    申请人:Zoller Gerhard
    公开号:US20080287448A1
    公开(公告)日:2008-11-20
    The invention relates to diacyl indazole derivatives of general formulae (I) or (II) and to the pharmaceutically acceptable salts thereof: Wherein X, R1 and R2 are as defined herein. The invention also relates to the use of these compounds as pharmaceutical products.
    该发明涉及一般式(I)或(II)的二酰基吲唑生物以及其药用可接受的盐:其中X,R1和R2如本文所定义。该发明还涉及将这些化合物用作药物产品。
  • [EN] BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES<br/>[FR] COMPOSÉS DE BENZAMIDE ET LEUR UTILISATION EN TANT QU'HERBICIDES
    申请人:BASF SE
    公开号:WO2019016385A1
    公开(公告)日:2019-01-24
    The present invention relates to benzamide compounds of the formula (I) and the N-oxides and salts thereof and to compositions comprising the same. The variables are as defined in the claims and the description. The invention also relates to the use of the benzamide compounds or of the compositions comprising such compounds for controlling unwanted vegetation. Furthermore, the invention relates to methods of applying such compounds.
    本发明涉及公式(I)的苯甲酰胺化合物及其N-氧化物和盐,以及包含它们的组合物。变量如权利要求和说明书中所定义。本发明还涉及使用苯甲酰胺化合物或包含这种化合物的组合物来控制不良植被。此外,本发明还涉及应用这种化合物的方法。
  • Process for the preparation of 1,4-disubstituted-5(4H)-tetrazolinones
    申请人:NIHON BAYER AGROCHEM K.K.
    公开号:EP0646577A1
    公开(公告)日:1995-04-05
    1,4-Disubstituted-5(4H)-tetrazolinones of the formula (I) (wherein R¹, R² and R³ have the meanings given in the specification), which are known to be useful as herbicides, can be obtained in very good yields by reacting the corresponding 1-substituted-5(4H)-tetrazolinones with the corresponding carbamoyl chlorides in the presence of 4-dimethylaminopyridine.
    式 (I) 的 1,4-二取代-5(4H)-四唑啉酮 将相应的 1-取代-5(4H)-四唑啉酮与相应的甲酰氯在 4-二甲氨基吡啶存在下进行反应,可获得收率极高的 1,4-二取代-5(4H)-四唑啉酮,该化合物已知可用作除草剂(其中 R¹、R² 和 R³ 的含义见说明书)。
  • DIACYLINDAZOL-DERIVATE ALS INHIBITOREN VON LIPASEN UND PHOSPHOLIPASEN
    申请人:sanofi-aventis
    公开号:EP1937648A1
    公开(公告)日:2008-07-02
  • US5767286A
    申请人:——
    公开号:US5767286A
    公开(公告)日:1998-06-16
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