1-(3-Chloro-4-hydroxyphenyl)propan-2-one | 84023-32-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-(3-Chloro-4-hydroxyphenyl)propan-2-one
• CAS: 84023-32-5
• 化学式: C₉H₉ClO₂
• mdl: MFCD03410443
• 分子量: 184.62
• InChiKey: DQBQBHYJXZYNNT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.222
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  1-(3-Chloro-4-hydroxyphenyl)-1-hydroxypropan-2-one 生成 1-(3-Chloro-4-hydroxyphenyl)propan-2-one
  参考文献：
  名称：

  EHNOMIYA, TAKUDZI;SIRAISI, YASUSI

  摘要：

  DOI：

文献信息

• Amine Substituted Methanesulfonamide Derivatives as Vanilloid Receptor Ligands
  申请人：Gruenenthal GmbH

  公开号：US20130079320A1

  公开（公告）日：2013-03-28

  The invention relates to amine substituted methanesulfonamide derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

  这项发明涉及胺取代甲磺酰胺衍生物作为辣椒素受体配体，以及含有这些化合物的药物组合物，还涉及这些化合物用于治疗和/或预防疼痛以及其他疾病和/或紊乱。
• ANTI-MUCUS DRUGS AND USES THEREFOR
  申请人：WASHINGTON UNIVERSITY

  公开号：US20150183777A1

  公开（公告）日：2015-07-02

  Disclosed are methods of identifying, generating and synthesizing compounds that inhibit MAPK13 activity. In various embodiments, compounds, salts thereof and prodrugs thereof of the present teachings can be useful for the treatment of diseases and disorders that involve excess mucus production.

  揭示了一种识别、生成和合成抑制MAPK13活性的化合物的方法。在各种实施方式中，本教导的化合物、其盐和前药可以用于治疗涉及过多粘液产生的疾病和紊乱。
• Processes for producing optically active 2-amino-1-phenylethanol derivatives
  申请人：Daicel Chemical Industries, Ltd.

  公开号：US20030143701A1

  公开（公告）日：2003-07-31

  An (R)-2-amino-1-phenylethanol derivative shown by the general formula (IIa) 1 wherein R 1 and R 5 represent a hydrogen atom, etc.; R 2 , R 3 and R 4 independently represent a halogen atom, etc., or a salt thereof, can readily be produced (1) by permitting a microorganism belonging to the genus Rhodosporidium, the genus Comamonas or the like to act on a mixture of corresponding (R)-form and (S)-form to asymmetrically utilize, or (2) by permitting a microorganism belonging to the genus Lodderomyces, the genus Pilimelia or the like to act on a corresponding aminoketone derivative to asymmetrically reduce. An (R,R)-1-phenyl-2-[(2-phenyl-1-alkylethyl)amino]ethanol derivative having a high optical purity can easily be obtained from the compound of the formula (IIa) or a salt thereof. Said derivative is useful as an intermediate for producing an anti-obesity agent and so on.

  通式（IIa）所示的（R）-2-氨基-1-苯乙醇衍生物，其中R1和R5代表氢原子等；R2、R3和R4分别独立地表示卤素原子等，或其盐，可以通过（1）让属于红孢霉属、普通小杆菌属或类似菌属的微生物作用于相应（R）-型和（S）-型的混合物以不对称利用，或（2）让属于洛德罗霉属、皮利米利亚属或类似菌属的微生物作用于相应的氨基酮衍生物以不对称还原而轻松制备。可以从式（IIa）化合物或其盐中轻松获得具有高光学纯度的（R，R）-1-苯基-2-［（2-苯基-1-烷基乙基）氨基］乙醇衍生物。所述衍生物可用作生产抗肥胖剂等中间体。
• Substituted Phenylureas and Phenylamides as Vanilloid Receptor Ligands
  申请人：FRANK Robert

  公开号：US20120258946A1

  公开（公告）日：2012-10-11

  Substituted phenylureas and phenylamides, processes for their preparation, pharmaceutical compositions containing these compounds, and the use of these compounds for preparing pharmaceutical compositions.

  取代苯基脲和苯基酰胺，其制备过程，含有这些化合物的制药组合物以及使用这些化合物制备制药组合物的用途。
• Arylethanol amine derivatives, their preparation and use in pharmaceutical compositions
  申请人：BEECHAM GROUP PLC

  公开号：EP0066351A1

  公开（公告）日：1982-12-08

  Compounds of formula (II); or a salt thereof; wherein R' is hydrogen or methyl: R2 is hydrogen or methyl; R3 is hydrogen, C1-12 C1-12 cycloalkyl, or benzyl optionally substituted with C1-6 alkyl, C1-6 alkoxy, or halogen, n is 1 or 2; and A is hydrogen, halogen, hydroxyl, C1-6 alkyl or C1-6 alkoxy; are useful in treating obesity, diabetes, or inflammation, or inhibiting platelet aggregation.

  式（II）化合物或其盐，其中 R' 是氢或甲基：R2 是氢或甲基；R3 是氢、C1-12 C1-12 环烷基或任选被 C1-6 烷基、C1-6 烷氧基或卤素取代的苄基，n 是 1 或 2；以及 A 是氢、卤素、羟基、C1-6 烷基或 C1-6 烷氧基；这些化合物可用于治疗肥胖症、糖尿病或炎症，或抑制血小板聚集。