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1,5-di-tert-butyl-3-methylpyrazole

中文名称
——
中文别名
——
英文名称
1,5-di-tert-butyl-3-methylpyrazole
英文别名
1,5-Ditert-butyl-3-methylpyrazole
1,5-di-tert-butyl-3-methylpyrazole化学式
CAS
——
化学式
C12H22N2
mdl
——
分子量
194.32
InChiKey
BLYWBSDVIHOKBW-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):
    3.2
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    叔丁基肼盐酸盐5-amino-2,2-dimethylhex-4-en-3-one二甲基亚砜 为溶剂, 反应 150.0h, 以86%的产率得到1,5-di-tert-butyl-3-methylpyrazole
    参考文献:
    名称:
    Scope and Limitations in the Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles from b-Amino Enones and Hydrazine Derivatives. 13C-Chemical Shift Prediction Rules for 1,3,5-Trisubstituted Pyrazoles
    摘要:
    DOI:
    10.3987/com-00-9102
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文献信息

  • Substituted Esters as Cannabinoid-1 Receptor Modulators
    申请人:Colandrea Vincent J.
    公开号:US20120135975A1
    公开(公告)日:2012-05-31
    Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, Alzheimer's disease, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, cirrhosis of the liver, non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), and the promotion of wakefulness.
    结构式(I)的新化合物是大麻素-1(CB1)受体的拮抗剂和/或反向激动剂,并且可用于治疗、预防和抑制由CB1受体介导的疾病。本发明的化合物可用作中枢作用药物,用于治疗精神病、记忆障碍、认知障碍、阿尔茨海默病、偏头痛、神经病、神经炎性疾病(包括多发性硬化症和格林-巴利综合征)以及病毒性脑炎、脑血管意外和头部创伤的炎症后遗症、焦虑症、压力、癫痫、帕金森病、运动障碍和精神分裂症。该化合物还可用于治疗物质滥用障碍、肥胖症或进食障碍、哮喘、便秘、慢性肠假性梗阻、肝硬化、非酒精性脂肪肝病(NAFLD)、非酒精性脂肪性肝炎(NASH)以及促进清醒。
  • Alberola, Angel; Gonzalez-Ortega, Alfonso; Sadaba, M. Luisa, Journal of the Chemical Society. Perkin transactions I, 1998, # 24, p. 4061 - 4065
    作者:Alberola, Angel、Gonzalez-Ortega, Alfonso、Sadaba, M. Luisa、Sanudo, M. Carmen
    DOI:——
    日期:——
  • Amide Compounds, Preparation Methods and Uses Thereof
    申请人:Liu Changling
    公开号:US20110046152A1
    公开(公告)日:2011-02-24
    Amide compounds, preparation methods and uses thereof. The structure of the compounds is represented as the general formula (I), in which the definitions of substituents are illuminated as description. The present amide compounds have broad spectrum activity of killing pests and are effective on lepidopteran pests including ostrinia nubilalis , sugarcane borer, adoxophyes orana fischer von reslerstamm, apple fruit borer, grapholitha inopinata, lymantri dispar l., cnaphalocrocis medinalis, ostrinia furnacalis, helicoverpa assulta, grapholitha inopinata, plutella xylostella, spodoptera exigua, prodenia litura etc., especially for plutella xylostella, spodoptera exigua . The present amide compounds can obtain good effect at very low dosage. At the same time, some compounds have good fungicidal activity which can be used to prevent rice blast, phytophthora infestans, cucumber downy mildew or grey mould of vegetables.
  • US8455398B2
    申请人:——
    公开号:US8455398B2
    公开(公告)日:2013-06-04
  • Scope and Limitations in the Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles from b-Amino Enones and Hydrazine Derivatives. 13C-Chemical Shift Prediction Rules for 1,3,5-Trisubstituted Pyrazoles
    作者:Alfonso González-Ortega、M. Luisa Sádaba、Angel Alberola、Luis Calvo Bleye、M. Carmen Sañudo
    DOI:10.3987/com-00-9102
    日期:——
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