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(3S)-3-methyl-2-pentanol | 1195650-01-1

中文名称
——
中文别名
——
英文名称
(3S)-3-methyl-2-pentanol
英文别名
(2Ξ,3S)-3-methyl-pentan-2-ol;(-)-(3S)-3-Methyl-pentanol-(2);(-)-(3S)-3-Methyl-pentan-2-ol;(3S)-3-Methyl-2-pentanol;(3S)-3-methylpentan-2-ol
(3S)-3-methyl-2-pentanol化学式
CAS
1195650-01-1
化学式
C6H14O
mdl
——
分子量
102.177
InChiKey
ZXNBBWHRUSXUFZ-ZBHICJROSA-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

物化性质

  • 沸点:
    136-137 °C
  • 密度:
    0.811±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (3S)-3-methyl-2-pentanol原甲酸三乙酯 生成 (+)-Tris-<(2S)-1,2-dimethyl-butyloxy>-methan
    参考文献:
    名称:
    Preparation of -(3S)-2,3-dimethylpentanal by reaction of (+)-tris[(2S)-1,2-dimethylbutoxy]methane (I) with carbon monoxide and hydrogen
    摘要:
    DOI:
    10.1021/jo01278a084
  • 作为产物:
    描述:
    (R)-<(S)-1-methylpropyl>oxirane 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 以66%的产率得到(3S)-3-methyl-2-pentanol
    参考文献:
    名称:
    Simple access to highly enantiomerically enriched (S)-3-methyl-1-pentanol, (S)-3-methyl-1-pentene, (2R,3S)-2-deuterio-3-methyl-1-pentanol and (2S,3S)-3-methyl-2-pentanol from natural (L)-isoleucine
    摘要:
    DOI:
    10.1021/jo00352a022
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文献信息

  • NOVEL NICOTINAMIDE DERIVATIVE OR SALT THEREOF
    申请人:FUJIFILM Corporation
    公开号:US20140309225A1
    公开(公告)日:2014-10-16
    The object of the present invention is to provide a compound and a pharmaceutical composition having excellent Syk inhibitory activity. According to the present invention, a nicotinamide derivative represented by the following formula (I) or a salt thereof is provided, wherein R 1 is a substituent represented by the following formula (II-1), (III-1), or (IV-1) (wherein R 3 , R 4 , R 5 , n, and X 1 have the same definitions as those described in the specification), and R 2 is a pyridyl, indazolyl, phenyl, pyrazolopyridyl, benzisoxazolyl, pyrimidinyl, or quinolyl group, each of which optionally has at least one substituent.
    本发明的目的是提供一种具有优异的Syk抑制活性的化合物和药物组合物。根据本发明,提供了由以下式(I)表示的烟酰胺衍生物或其盐, 其中 R 1 是由以下式(II-1)、(III-1)或(IV-1)表示的取代基 (其中R 3 、R 4 、R 5 、n和X 1 的定义与说明书中描述的相同),而R 2 是吡啶基、吲唑基、苯基、吡唑吡啶基、苯并异噁唑基、嘧啶基或喹啉基,每种基可选择地具有至少一个取代基。
  • [EN] PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER<br/>[FR] DÉRIVÉS DE LA PIPÉRIDINONE EN TANT QU'INHIBITEURS DE MDM2 POUR LE TRAITEMENT DU CANCER
    申请人:AMGEN INC
    公开号:WO2011153509A1
    公开(公告)日:2011-12-08
    The present invention provides MDM2 inhibitor compounds of Formula (I), wherein the variables are defined above, which compounds are useful as therapeutic agents, particularly for the treatment of cancers. The present invention also relates to pharmaceutical compositions that contain an MDM2 inhibitor.
    本发明提供了式(I)的MDM2抑制剂化合物,其中变量如上所定义,这些化合物可用作治疗剂,特别是用于癌症的治疗。本发明还涉及含有MDM2抑制剂的药物组合物。
  • Compounds for the Treatment of Hepatitis C
    申请人:Bristol-Myers Squibb Company
    公开号:US20130203758A1
    公开(公告)日:2013-08-08
    The disclosure provides compounds of formula I, including pharmaceutically acceptable salts, as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.
    该披露提供了化合物I的公式,包括药用可接受的盐,以及使用这些化合物的组合物和方法。这些化合物对丙型肝炎病毒(HCV)具有活性,并可能在治疗感染HCV的患者中有用。
  • PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER
    申请人:AMGEN INC.
    公开号:US20140315895A1
    公开(公告)日:2014-10-23
    The present invention provides MDM2 inhibitor compounds of Formula I, wherein the variables are defined above, which compounds are useful as therapeutic agents, particularly for the treatment of cancers. The present invention also relates to pharmaceutical compositions that contain an MDM2 inhibitor.
    本发明提供了MDM2抑制剂化合物I的公式,其中变量如上所定义,这些化合物可用作治疗剂,特别是用于治疗癌症。本发明还涉及包含MDM2抑制剂的制药组合物。
  • Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer
    申请人:AMGEN INC.
    公开号:US20160137667A1
    公开(公告)日:2016-05-19
    The present invention provides MDM2 inhibitor compounds of Formula I, wherein the variables are defined above, which compounds are useful as therapeutic agents, particularly for the treatment of cancers. The present invention also relates to pharmaceutical compositions that contain an MDM2 inhibitor.
    本发明提供了式I的MDM2抑制剂化合物,其中变量如上所定义,该化合物可用作治疗剂,特别是用于治疗癌症。本发明还涉及含有MDM2抑制剂的制药组合物。
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