3-氯-4-甲氧基苯脒盐酸盐 | 126007-98-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 中文名称: 3-氯-4-甲氧基苯脒盐酸盐
• 英文名称: 3-chloro-4-methoxybenzimidamide hydrochloride
• 英文别名: 3-Chloro-4-methoxybenzamidine hydrochloride；3-Chloro-4-methoxybenzene-1-carboximidamide hydrochloride；3-chloro-4-methoxybenzenecarboximidamide;hydrochloride
• CAS: 126007-98-5
• 化学式: C₈H₉ClN₂O*ClH
• 分子量: 221.086
• InChiKey: SYVZCZVIURXKBE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.05
• 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：
  59.1
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-氯-4-甲氧基苯脒盐酸盐 生成 2-(3-Chloro-4-methoxyphenyl)-4-(thien-2-yl)-imidazole
  参考文献：
  名称：

  摘要：

  DOI：
• 作为产物：
  描述：

  methyl-3-chloro-4-methoxybenzimidate hydrochloride 生成 3-氯-4-甲氧基苯脒盐酸盐
  参考文献：
  名称：

  摘要：

  DOI：

文献信息

• [EN] SUBSTITUTED CONDENSED PYRIMIDINE COMPOUNDS<br/>[FR] COMPOSÉS DE PYRIMIDINE CONDENSÉS SUBSTITUÉS
  申请人：GRUENENTHAL GMBH

  公开号：WO2014170020A1

  公开（公告）日：2014-10-23

  The invention relates to novel substituted condensed pyrimidine compounds of general formula (I) in which the chemical groupings, substituents and indices are as defined in the description, and to their use as medicaments, in particular as medicaments for the treatment of conditions and diseases that can be treated by inhibition of the PDE4 enzyme.

  本发明涉及通式(I)的新型取代的稠合嘧啶化合物，其中化学基团、取代基和指数如说明书中所定义，以及它们作为药物的用途，特别是作为治疗可通过抑制PDE4酶治疗的病症和疾病的药物。
• .beta.-adrenergic blocking imidazolylphenoxy propanolamines
  申请人：Merck & Co., Inc.

  公开号：US04642311A1

  公开（公告）日：1987-02-10

  Substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and .beta.-adrenergic blocking activity. ##STR1##

  公开了取代咪唑和其制备方法。这些咪唑及其盐表现出药理活性，包括降压活性和β-肾上腺素受体阻滞活性。
• .beta.-blocking substituted imidazoles
  申请人：Merck & Co., Inc.

  公开号：US04853383A1

  公开（公告）日：1989-08-01

  Novel substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and .beta.-adrenergic blocking activity.

  揭示了一种新型替代咪唑并其制备方法。这些咪唑及其盐具有药理活性，包括抗高血压活性和β-肾上腺素能阻断活性。
• Imidazotriazines for use as phosphodiesterase inhibitors
  申请人：——

  公开号：US20040249148A1

  公开（公告）日：2004-12-09

  The invention relates to new imidazotriazines, processes for their preparation, and their use for the production of medicaments for the treatment and/or prophylaxis of neurodegenerative disorders, in particular Parkinson's disease.

  本发明涉及新的咪唑三嗪类化合物，其制备方法以及它们在制备用于治疗和/或预防神经退行性疾病的药物中的应用，特别是帕金森病。
• NOVEL SUBSTITUTED CONDENSED PYRIMIDINE COMPOUNDS
  申请人：GRÜNENTHAL GMBH

  公开号：US20160031857A1

  公开（公告）日：2016-02-04

  The invention relates to novel substituted condensed pyrimidine compounds of general formula (I) in which the chemical groupings, substituents and indices are as defined in the description, and to their use as medicaments, in particular as medicaments for the treatment of conditions and diseases that can be treated by inhibition of the PDE4 enzyme.

  本发明涉及新颖的取代紧缩嘧啶化合物，其一般式为(I)，其中化学基团、取代基和下标如描述中所定义，并且涉及它们作为药物的用途，特别是作为用于抑制PDE4酶治疗可以通过抑制PDE4酶治疗的情况和疾病的药物。