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2,2-二甲基-1-[(2-甲基-2-丙基)氧基]丙烷 | 32970-46-0

中文名称
2,2-二甲基-1-[(2-甲基-2-丙基)氧基]丙烷
中文别名
——
英文名称
Neopentyl-tert.-butyl-ether
英文别名
1-tert-butoxy-2,2-dimethyl-propane;2,2-Dimethyl-1-[(2-methylpropan-2-yl)oxy]propane
2,2-二甲基-1-[(2-甲基-2-丙基)氧基]丙烷化学式
CAS
32970-46-0
化学式
C9H20O
mdl
——
分子量
144.257
InChiKey
QAROENULPPDYNI-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):
    2.8
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2909199090

SDS

SDS:7f9ff5e1b775ce2e80294e7d052823fe
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反应信息

  • 作为产物:
    参考文献:
    名称:
    Gas-phase nucleophilic displacement reactions
    摘要:
    利用脉冲离子回旋共振(ICR)谱学研究了各种阴离子亲核试剂与各种中性分子之间的取代反应。通过对反应速率常数的解析,将其归结为三步反应序列。采用RRKM计算方法来获取过渡态能量的信息。此外,还讨论了溶液中反应势垒的起源。
    DOI:
    10.1002/jms.1190301204
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文献信息

  • Macrocyclic Modulators of the Ghrelin Receptor
    申请人:Ocera Therapeutics, Inc.
    公开号:US20180110824A1
    公开(公告)日:2018-04-26
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
    本发明提供了一种新颖的构象定义明确的大环化合物,已经证明是生长激素分泌素受体(GHS-R1a及其亚型、异构体和变体)的选择性调节剂。本文还描述了合成这些新型化合物的方法。这些化合物可用作生长激素分泌素受体的激动剂,用于治疗和预防一系列医疗状况,包括但不限于代谢和/或内分泌紊乱、胃肠道紊乱、心血管疾病、肥胖和与肥胖相关的疾病、中枢神经系统疾病、遗传疾病、过度增殖性疾病和炎症性疾病。
  • HEPATITIS C VIRUS INHIBITORS AND USES THEREOF IN PREPARATION OF DRUGS
    申请人:CHANGZHOU YINSHENG PHARMACEUTICAL CO., LTD.
    公开号:US20170253614A1
    公开(公告)日:2017-09-07
    A series of hepatitis C virus (HCV) inhibitors and compositions and applications thereof in the preparation of drugs for treating chronic HCV infection. Especially, a series of compounds that are used as NS5A inhibitors, and compositions and uses thereof in the preparations of drugs.
    一系列丙型肝炎病毒(HCV)抑制剂及其组合物,以及在制备用于治疗慢性HCV感染的药物时的应用。特别是一系列用作NS5A抑制剂的化合物,以及在药物制剂中的组合物和用途。
  • CHEMOKINE RECEPTOR ANTAGONISTS AND METHODS OF USE THEREOF
    申请人:Millennium Pharmaceuticals, Inc.
    公开号:US20160031908A1
    公开(公告)日:2016-02-04
    Disclosed are novel compounds and a method of treating a disease associated with aberrant leukocyte recruitment and/or activation. The method comprises administering to a subject in need an effective amount of a compound represented by: or physiologically acceptable salt thereof.
    揭示了新颖的化合物以及治疗与异常白细胞召集和/或激活相关的疾病的方法。该方法包括向需要的受试者施用代表的化合物的有效量: 或其生理上可接受的盐。
  • THERAPEUTIC COMPOUNDS
    申请人:REGENTS OF THE UNIVERSITY OF MINNESOTA
    公开号:US20160376238A1
    公开(公告)日:2016-12-29
    The invention provides compounds of formula (I): wherein, A, C, D, X, and Y have any of the values defined in the specification, and salts thereof. The compounds are SIRT2 inhibitors and are useful for treating SIRT2 associated conditions.
    这项发明提供了式(I)的化合物: 其中,A、C、D、X 和 Y 可以取规范中定义的任何值,以及它们的盐。这些化合物是SIRT2抑制剂,可用于治疗与SIRT2相关的疾病。
  • Methylphenidate-Prodrugs, Processes of Making and Using the Same
    申请人:KemPharm, Inc.
    公开号:US20150266911A1
    公开(公告)日:2015-09-24
    The present technology is directed to prodrugs and compositions for the treatment of various diseases and/or disorders comprising methylphenidate, or methylphenidate derivatives, conjugated to at least one alcohol, amine, oxoacid, thiol, or derivatives thereof. In some embodiments, the conjugates further include at least one linker. The present technology also relates to the synthesis of methylphenidate, or methylphenidate derivatives, conjugated to at least one alcohol, amine, oxoacid, thiol, or derivatives thereof or combinations thereof.
    目前的技术是针对前药和组合物的,用于治疗包括甲基苯丙胺或甲基苯丙胺衍生物的至少与醇、胺、羧酸、硫醇或其衍生物结合的各种疾病和/或紊乱。在某些实施例中,这些结合物还包括至少一个连接剂。该技术还涉及合成甲基苯丙胺或甲基苯丙胺衍生物,结合至少一个醇、胺、羧酸、硫醇或其衍生物或其组合的方法。
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