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2,4-二氯-3-氨基苯酚盐酸盐 | 61693-43-4

中文名称
2,4-二氯-3-氨基苯酚盐酸盐
中文别名
3-氨基-2,4-二氯苯酚盐酸盐;3-氨基-2,4-二氯苯酚HCL
英文名称
2,4-dichloro-3-aminophenol hydrochloride
英文别名
3-amino-2,4-dichlorophenol hydrochloride;2,4-dichloro-3-aminophenol-hydrochloride;3-amino-2,4-dichlorophenol;hydrochloride
2,4-二氯-3-氨基苯酚盐酸盐化学式
CAS
61693-43-4
化学式
C6H5Cl2NO*ClH
mdl
——
分子量
214.479
InChiKey
MQWQWQBIVSVACH-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):
    2.7
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    3
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2922299090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:1b22fecd7495d443637ff628c413032f
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反应信息

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文献信息

  • [EN] PYRIMIDINE UREA DERIVATIVES AS KINASE INHIBITORS<br/>[FR] DERIVES PYRIMIDINES UREE EN TANT QU'INHIBITEURS DE KINASE
    申请人:NOVARTIS AG
    公开号:WO2006000420A1
    公开(公告)日:2006-01-05
    The invention relates to compounds of formula (I) wherein the substituents X1, R1, R2, R3 and R4 have the meaning as set forth and explained in the description of the invention, to processes for the preparation of these compounds, pharmaceutical compositions containing same, the use thereof optionally in combination with one or more other pharmaceutically active compounds for the therapy of a disease which responds to an inhibition of protein kinase activity, and a method for the treatment of such a disease.
    该发明涉及式(I)的化合物,其中取代基X1、R1、R2、R3和R4的含义如所述并解释在该发明的描述中,以及制备这些化合物的方法,含有相同化合物的药物组合物,可选择与一个或多个其他药用活性化合物结合使用,用于治疗对蛋白激酶活性抑制有反应的疾病,并且用于治疗此类疾病的方法。
  • [EN] COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF PREPARING COMPOUNDS AND OF THEIR USE<br/>[FR] COMPOSÉS, COMPOSITIONS PHARMACEUTIQUES ET PROCÉDÉS DE PRÉPARATION ET D'UTILISATION ASSOCIÉS
    申请人:REPARE THERAPEUTICS INC
    公开号:WO2021195781A1
    公开(公告)日:2021-10-07
    Disclosed are compounds and pharmaceutically acceptable salts thereof that may be used in the treatment of subjects in need thereof. The compounds disclosed herein may be inhibitors of tyrosine and threonine-specific cdc2-inhibitory kinase (Myt1). Also disclosed are pharmaceutical compositions containing the compounds or pharmaceutically acceptable salts thereof and methods of their preparation and use.
    本文披露了化合物及其药用盐,可用于治疗需要的对象。本文披露的化合物可能是酪氨酸和苏氨酸特异性cdc2抑制激酶(Myt1)的抑制剂。还披露了含有这些化合物或其药用盐的药物组合物,以及其制备和使用方法。
  • Coupler components for the oxidation of hair dyes and their use, as well
    申请人:Henkel Kommanditgesellschaft auf Aktien
    公开号:US04402699A1
    公开(公告)日:1983-09-06
    2,4-Dichloro-3-alkylidene-aminophenols having the formula: ##STR1## wherein R.sub.1 represents hydrogen or an alkyl radical having 1 to 6 carbon atoms and R.sub.2 represents an alkyl radical having 1 to 6 carbon atoms or an aryl radical, with the proviso that R.sub.2 can only be an aryl radical when R.sub.1 is hydrogen. The 2,4-dichloro-alkylidene-aminophenols can be produced by reaction of 2,4-dichloro-3-aminophenol with the corresponding aldehydes or ketones. They are suitable as such, or in the form of their salts with inorganic or organic acids, as coupler components in oxidation hair dyes.
    具有以下公式的2,4-二氯-3-烷基亚胺基酚:##STR1## 其中R.sub.1代表氢或具有1至6个碳原子的烷基基团,而R.sub.2代表具有1至6个碳原子的烷基基团或芳基基团,但前提是当R.sub.1为氢时,R.sub.2只能是芳基基团。2,4-二氯-烷基亚胺基酚可以通过2,4-二氯-3-氨基酚与相应的醛或酮反应制备而成。它们适用于氧化染发剂中的偶合剂成分,可以作为其盐的形式与无机或有机酸一起使用。
  • Compounds and compositions as protein kinase inhibitors
    申请人:Ding Qiang
    公开号:US08552002B2
    公开(公告)日:2013-10-08
    The invention relates to compounds of formula (I) wherein the substituents X1, R1, R2, R3 and R4 have the meaning as set forth and explained in the description of the invention, to processes for the preparation of these compounds, pharmaceutical compositions containing same, the use thereof optionally in combination with one or more other pharmaceutically active compounds for the therapy of a disease which responds to an inhibition of protein kinase activity, and a method for the treatment of such a disease.
    本发明涉及公式(I)的化合物,其中取代基X1,R1,R2,R3和R4的含义如本发明说明书所述和解释的那样,以及制备这些化合物的过程,包含它们的药物组合物,可选地与一种或多种其他药物活性化合物结合使用以治疗对蛋白激酶活性抑制有反应的疾病,以及治疗这种疾病的方法。
  • COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS
    申请人:DING Qiang
    公开号:US20130012476A1
    公开(公告)日:2013-01-10
    The invention relates to compounds of formula (I) wherein the substituents X 1 , R 1 , R 2 , R 3 and R 4 have the meaning as set forth and explained in the description of the invention, to processes for the preparation of these compounds, pharmaceutical compositions containing same, the use thereof optionally in combination with one or more other pharmaceutically active compounds for the therapy of a disease which responds to an inhibition of protein kinase activity, and a method for the treatment of such a disease.
    本发明涉及公式(I)的化合物,其中取代基X1、R1、R2、R3和R4的含义如发明说明中所述和解释的那样,以及制备这些化合物的方法、包含它们的药物组合物,其可选择与一个或多个其他药理活性化合物结合使用,用于治疗对蛋白激酶活性抑制有反应的疾病,以及用于治疗这种疾病的方法。
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