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2-氯-6-氟-3-甲基苯酚 | 261762-90-7

中文名称
2-氯-6-氟-3-甲基苯酚
中文别名
——
英文名称
2-chloro-6-fluoro-3-methylphenol
英文别名
——
2-氯-6-氟-3-甲基苯酚化学式
CAS
261762-90-7
化学式
C7H6ClFO
mdl
MFCD01631366
分子量
160.575
InChiKey
RPTGCWUNGWVQET-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:
    47-50℃
  • 沸点:
    211°C
  • 密度:
    1.334±0.06 g/cm3(Predicted)
  • 闪点:
    211°C

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险等级:
    8

反应信息

  • 作为反应物:
    描述:
    2-氯-6-氟-3-甲基苯酚N-溴代丁二酰亚胺(NBS) 作用下, 以 四氢呋喃 为溶剂, 反应 0.17h, 生成 4-bromo-2-chloro-6-fluoro-3-methylphenol
    参考文献:
    名称:
    [EN] NEW THIENOPYRIMIDINE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    [FR] NOUVEAUX DÉRIVÉS DE THIÉNOPYRIMIDINE, PROCÉDÉ POUR LEUR PRÉPARATION ET COMPOSITIONS PHARMACEUTIQUES LES CONTENANT
    摘要:
    式(I)的化合物:其中R1、R2、R3、R4、R5、R6、R7、R12、X、A和n的定义如描述中所述。
    公开号:
    WO2015097123A1
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文献信息

  • Primary Amines as Renin Inhibitors
    申请人:Bezencon Olivier
    公开号:US20090088457A1
    公开(公告)日:2009-04-02
    The invention relates to novel primary amine derivatives and the use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.
    这项发明涉及新型一次胺衍生物及其在制备药物组合物中作为活性成分的用途。该发明还涉及相关方面,包括制备这些化合物的过程、含有其中一种或多种化合物的药物组合物,特别是它们作为肾素抑制剂的用途。
  • [EN] DIAZABICYCLONONENE AND TETRAHYDROPYRIDINE DERIVATIVES AS RENIN INHIBITORS<br/>[FR] DERIVES DE DIAZABICYCLONONENE ET DE TETRAHYDROPYRIDINE UTILISES COMME INHIBITEURS DE LA RENINE
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2004096804A1
    公开(公告)日:2004-11-11
    The invention relates to novel 3,9-diazabicyclo[3.3.1]nonene derivatives, tetrahydropyridine derivatives, and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.
    本发明涉及新型的3,9-二氮杂双环[3.3.1]壬烯衍生物、四氢吡啶衍生物及其相关化合物,以及它们作为活性成分用于制备药物组合物的用途。本发明还涉及相关方面,包括制备这些化合物的方法、含有一种或多种这些化合物的药物组合物,尤其是它们作为肾素抑制剂的用途。
  • Novel Piperidine Carboxylic Acid Amide Derivatives
    申请人:Bezencon Olivier
    公开号:US20080214598A1
    公开(公告)日:2008-09-04
    The invention relates to novel piperidine carboxylic acid amide derivatives and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of these novel compounds, pharmaceutical compositions comprising such compounds and especially the use of such compounds as inhibitors of renin.
    本发明涉及新型的哌啶羧酸酰胺衍生物及其作为活性成分用于制备药物组合物。本发明还涉及相关方面,包括这些新型化合物的制备方法、包含此类化合物的药物组合物,尤其是此类化合物作为肾素抑制剂的应用。
  • [EN] BICYCLONONENE DERIVATIVES AS RENIN INHIBITORS<br/>[FR] DÉRIVÉS DU BICYCLONONÈNE EMPLOYÉS EN TANT QU'INHIBITEURS DE LA RÉNINE
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2006021402A1
    公开(公告)日:2006-03-02
    The invention relates to novel bicyclononene derivatives of Formula (I); and the use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.
    该发明涉及公式(I)的新型双环庚烯衍生物;以及其作为药物组合物中活性成分的用途。该发明还涉及相关方面,包括制备化合物的方法,含有其中一种或多种化合物的药物组合物,特别是它们作为肾素抑制剂的用途。
  • 3-(PHENOXYPHENYLMETHYL)PYRROLIDINE COMPOUNDS
    申请人:Stangeland Eric
    公开号:US20100022616A1
    公开(公告)日:2010-01-28
    In one aspect, the invention relates to compounds of formula I: where a and R 1-6 are as defined in the specification, or a pharmaceutically acceptable salt thereof. The compounds of formula I are serotonin and norepinephrine reuptake inhibitors. In another aspect, the invention relates to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.
    在一个方面,该发明涉及到以下式I的化合物:其中a和R1-6如规范中所定义,或其药用可接受盐。式I的化合物是血清素和去甲肾上腺素再摄取抑制剂。在另一个方面,该发明涉及到包含这些化合物的药物组合物;使用这些化合物的方法;以及制备这些化合物的工艺和中间体。
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