2-(3-羟基-4-甲基苯基)乙腈 | 103264-70-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2-(3-羟基-4-甲基苯基)乙腈
• 英文名称: 2-(3-hydroxy-4-methylphenyl)acetonitrile
• 英文别名: 3-Hydroxy-4-methylphenylacetonitrile
• CAS: 103264-70-6
• 化学式: C₉H₉NO
• 分子量: 147.177
• InChiKey: QAOJXZSPCDKVBM-UHFFFAOYSA-N

物化性质

• 沸点：
  309.0±27.0 °C(Predicted)
• 密度：
  1.129±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  44
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(3-羟基-4-甲基苯基)乙腈 在 sodium azide 、 potassium carbonate 、 氯化铵 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 32.0h， 生成 5-(3-(2,6-dimethylbenzyloxy)-4-methylbenzyl)-1H-tetrazole
  参考文献：
  名称：

  TETRAZOLE COMPOUNDS FOR REDUCING URIC ACID

  摘要：

  公开号：

  EP2282736B1
• 作为产物：
  描述：

  6-acetoxy-6-methylcyclohexa-2,4-dienone 在 sodium hydroxide 作用下， 生成 2-(3-羟基-4-甲基苯基)乙腈
  参考文献：
  名称：

  Ultrasonographic, Axial, and Peripheral Measurements in Female Patients with Benign Hypermobility Syndrome

  摘要：

  Twenty-five female Caucasians, aged 19-57 years, with the hypermobility syndrome had bone density measurements using established noninvasive techniques such as dual X-ray absorptiometry (DXA), single photon absorptiometry (SPA), heel ultrasound (US), and peripheral computed tomography (pQCT) acquisitions of the radius. As a group, comparisons of the different bone indices with the corresponding age-matched reference population resulted in normal z-scores for the arial densities, however, values for the volumetric total and cortical bone at the radius measured by pQCT were significantly lower than expected (P < 0.0001). Spinal and femoral bone density results were significant after correction for body mass index (BMI). This cross-sectional study shows that the benign hypermobility syndrome patients have lowered t-scores for data reflecting bone structure and bone strength as measured with US and the tomographic technique.

  DOI：

  10.1007/s00223001093

文献信息

• Non-nucleoside reverse transcriptase inhibitors
  申请人：Roche Palo Alto LLC

  公开号：US20040192704A1

  公开（公告）日：2004-09-30

  This invention relates to novel heterocyclic compounds of formula I wherein R 1 —R 4 , X 1 and X 2 are as defined in the summary and pharmaceutically acceptable salts and solvates thereof, methods to inhibit or modulate Human Immunodeficiency Virus (HIV) reverse transcriptase with compounds of formula I, pharmaceutical compositions containing of formula I admixed with at least one solvent, carrier or excipient and processes to prepare compounds of formula I. The compounds are useful for treating disorders in which HIV and genetically related viruses are implicated 1

  这项发明涉及公式I的新异环化合物，其中R1-R4、X1和X2如摘要中所定义，并且其药用可接受盐和溶剂化合物，用公式I的化合物抑制或调节人类免疫缺陷病毒（HIV）逆转录酶的方法，含有公式I的药物组合物，与至少一种溶剂、载体或赋形剂混合，并制备公式I的化合物的方法。这些化合物可用于治疗HIV和遗传相关病毒参与的疾病。
• SUBSTITUTED 2-[2-(PHENYL) ETHYLAMINO] ALKANEAMIDE DERIVATIVES AND THEIR USE AS SODIUM AND/OR CALCIUM CHANNEL MODULATORS
  申请人：Melloni Piero

  公开号：US20100210631A1

  公开（公告）日：2010-08-19

  Substituted 2-[2-(phenyl)ethylamino]alkaneamide derivatives, pharmaceutically acceptable salts thereof, and pharmaceutical compositions containing them are useful as sodium and/or calcium channel modulators for preventing, alleviating and curing pathologies wherein the above mechanisms play a pathological role. The compounds may be particularly used for the prevention, alleviation, and curing of, for example, neurological, cognitive, psychiatric, inflammatory, urogenital, and gastrointestinal diseases.

  2-[2-(苯基)乙基氨基]烷酰胺衍生物及其药用盐以及含有它们的药物组合物可用作钠和/或钙通道调节剂，用于预防、缓解和治疗上述机制发挥病理作用的病变。这些化合物特别可用于预防、缓解和治疗例如神经、认知、精神、炎症、泌尿生殖以及胃肠疾病等病症。
• Nonnucleoside reverse transcriptase inhibitors
  申请人：Dunn Patrick James

  公开号：US20070179157A1

  公开（公告）日：2007-08-02

  This invention relates to methods of treating an HIV infection with novel heterocyclic compounds of formula I wherein R 1 —R 4 , X 1 and X 2 are as defined in the summary and pharmaceutically acceptable salts, and methods to inhibit or modulate Human Immunodeficiency Virus (HIV) reverse transcriptase with compounds of formula I.

  本发明涉及使用公式I中的新异环化合物治疗HIV感染的方法，其中R1-R4，X1和X2如摘要中所定义，并且包括药学上可接受的盐，以及使用公式I中的化合物抑制或调节人类免疫缺陷病毒（HIV）反转录酶的方法。
• Modulators of ATP-Binding Cassette Transporters
  申请人：Ruah Sara S. Hadida

  公开号：US20110071206A1

  公开（公告）日：2011-03-24

  Compounds of the present invention and pharmaceutically acceptable compositions thereof, are useful as modulators of ATP-Binding Cassette (“ABC”) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator (“CFTR”). The present invention also relates to methods of treating ABC transporter mediated diseases using compounds of the present invention.

  本发明的化合物及其药学上可接受的组合物可用作ATP结合盒（“ABC”）转运蛋白或其片段的调节剂，包括囊性纤维化跨膜导电调节因子（“CFTR”）。本发明还涉及使用本发明的化合物治疗ABC转运蛋白介导的疾病的方法。
• Substituted 2-[2-(phenyl) ethylamino] alkaneamide derivatives and their use as sodium and/or calcium channel modulators
  申请人：Newron Pharmaceuticals S.P.A.

  公开号：US09051240B2

  公开（公告）日：2015-06-09

  Substituted 2-[2-(phenyl)ethylamino]alkaneamide derivatives, pharmaceutically acceptable salts thereof, and pharmaceutical compositions containing them are useful as sodium and/or calcium channel modulators for preventing, alleviating and curing pathologies wherein the above mechanisms play a pathological role. The compounds may be particularly useful for the prevention, alleviation, and curing of, for example, neurological, cognitive, psychiatric, inflammatory, urogenital and gastrointestinal diseases.

  替代2-[2-(苯基)乙基氨基]烷酰胺衍生物，其药学上可接受的盐以及含有它们的制药组合物可作为钠和/或钙通道调节剂，用于预防、缓解和治疗上述机制在病理学作用的病理学。这些化合物可能特别有用于预防、缓解和治疗例如神经、认知、精神、炎症、泌尿生殖和胃肠疾病。