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(3-methoxycyclobutyl)methanol | 2092237-60-8

中文名称
——
中文别名
——
英文名称
(3-methoxycyclobutyl)methanol
英文别名
——
(3-methoxycyclobutyl)methanol化学式
CAS
2092237-60-8;864867-28-7
化学式
C6H12O2
mdl
——
分子量
116.16
InChiKey
XIICKNMLKKNTGN-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):
    0.2
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

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文献信息

  • NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS
    申请人:Carroll William A.
    公开号:US20090105306A1
    公开(公告)日:2009-04-23
    The present invention relates compounds of formula (I) wherein A and R 1 are as defined in the specification, pharmaceutical compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and pharmaceutical compositions.
    本发明涉及以下式(I)的化合物 其中A和R1如规范中所定义,包括这些化合物的药物组合物,以及使用这些化合物和药物组合物治疗疾病和疾病的方法。
  • COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS
    申请人:Carroll William A.
    公开号:US20100249129A1
    公开(公告)日:2010-09-30
    Disclosed herein are compounds of formula (I) wherein Ring A and R 1 are as defined in the specification. Pharmaceutical compositions comprising such compounds, and methods for treating conditions and disorders using such compounds and pharmaceutical compositions are also disclosed.
    本文揭示了以下式(I)的化合物 其中环A和R 1 如规范中所定义。还披露了包含这些化合物的药物组合物,以及使用这些化合物和药物组合物治疗疾病和疾病的方法。
  • NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS AND USES THEREOF
    申请人:Florjancic S. Alan
    公开号:US20080058335A1
    公开(公告)日:2008-03-06
    The present invention relates to compounds of formula (I), or pharmaceutical salts, prodrugs, salts of prodrugs, or combinations thereof, wherein R 1 , R 2 , R 3 , and L 1 are defined in the specfication, compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and compositions. The present invention also relates to compounds of formula (II), or pharmaceutical salts, prodrugs, salts of prodrugs, or combinations thereof, wherein R 1a , R 2a and (Rx)n are as defined in the specification, compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and compositions.
    本发明涉及式(I)的化合物,或药用盐、前药、前药的盐或其组合物, 其中R 1 ,R 2 ,R 3 和L 1 在规范中定义,包含这种化合物的组合物,以及使用这种化合物和组合物治疗疾病和疾病的方法。本发明还涉及式(II)的化合物,或药用盐、前药、前药的盐或其组合物, 其中R 1a ,R 2a 和(Rx)n如规范中定义,包含这种化合物的组合物,以及使用这种化合物和组合物治疗疾病和疾病的方法。
  • 3-(5-HYDROXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF
    申请人:Novartis AG
    公开号:US20200017461A1
    公开(公告)日:2020-01-16
    The present disclosure provides a compound of Formula (I′): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein R x , X 1 , X 2 , and R 1 are as defined herein, and methods of making and using same.
    本公开提供了化合物Formula (I′)的一种: 或其药用可接受的盐、合物、溶剂合物、前药、立体异构体或互变异构体,其中R x 、X 1 、X 2 和R 1 如本文所定义,并提供了制备和使用该化合物的方法。
  • [EN] C5-C6-OXACYCLIC FUSED IMINOPYRIMIDINONE COMPOUNDS AS BACE INHIBITORS, COMPOSITIONS, AND THEIR USE<br/>[FR] COMPOSÉS IMINOPYRIMIDINONES CONDENSÉS OXACYCLIQUES EN C5-C6 UTILISÉS COMME INHIBITEURS DE BACE, COMPOSITIONS ET UTILISATION ASSOCIÉES
    申请人:MERCK SHARP & DOHME
    公开号:WO2016085780A1
    公开(公告)日:2016-06-02
    In its many embodiments, the present invention provides certain C5-C6-oxacyclic fused iminopyrimidinone compounds, including compounds Formula (I): or a tautomer thereof, and pharmaceutically acceptable salts of said compounds and said tautomers, wherein RN, R1, RA, ring A, m, n, -L1-, ring B, RB, and p are as defined herein. The novel compounds of the invention are useful as BACE inhibitors and/or for the treatment and prevention of various pathologies related thereto. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use, including for the possible treatment of Alzheimer's disease, are also disclosed.
    在其多种实施方式中,本发明提供了某些C5-C6-氧杂环融合咪唑嘧啶酮化合物,包括化合物式(I)所示的化合物或其互变异构体,以及该化合物和该互变异构体的药学上可接受的盐,其中RN、R1、RA、环A、m、n、-L1-、环B、RB和p如本文所定义。本发明的新化合物可用作BACE抑制剂和/或用于治疗和预防与之相关的各种病理。还披露了包括一种或多种此类化合物(单独使用和与一种或多种其他活性剂组合使用)的药物组合物,以及其制备和使用方法,包括可能用于治疗阿尔茨海默病的方法。
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