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(1S,3R)-3-Ethyl-cyclopentanol | 87759-47-5

中文名称
——
中文别名
——
英文名称
(1S,3R)-3-Ethyl-cyclopentanol
英文别名
(1S,3R)-3-ethylcyclopentan-1-ol
(1S,3R)-3-Ethyl-cyclopentanol化学式
CAS
87759-47-5
化学式
C7H14O
mdl
——
分子量
114.188
InChiKey
CRHZGBUSTWVQAQ-RQJHMYQMSA-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):
    1.8
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • 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

反应信息

  • 作为反应物:
    描述:
    甲氧基-三氟甲基苯(1S,3R)-3-Ethyl-cyclopentanol 在 sodium tetrahydroborate 、 1,4-dihydronicotinamide adenine dinucleotide 、 horse liver alcohol dehydrogenase 、 (±)-α-甲氧基-α-(三氟甲基)苯乙酸 作用下, 生成 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,3R)-3-ethyl-cyclopentyl ester 、 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,3S)-3-ethyl-cyclopentyl ester 、 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,3R)-3-ethyl-cyclopentyl ester 、 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,3S)-3-ethyl-cyclopentyl ester
    参考文献:
    名称:
    Use of shift reagent with MTPA derivatives in19F NMR spectrocopy: IV—Determination of enantiomeric composition for a variety of secondary cycloalkanols. A survey
    摘要:
    AbstractChiral secondary cycloalkanols (monocyclic alcohols) are derivatized to the corresponding (R)‐α‐methoxy‐α‐trifluoromethyl‐α‐phenylacetic acid [(R)‐MTPA] esters and analysed by 19F NMR in the presence of tris(6,6,7,7,8,8,8‐heptafluoro‐2,2‐dimethyl‐3,5‐octanedionato) europium(III) [Eu(fod)3]. Using this method the enantiomeric composition can be measured for several cyclopentanols, cyclohexanols and cycloheptanols, with a variety of substitution patterns. It is shown that a mixture of four stereoisomeric cycloalkanols, such as cis and trans disubstituted alcohols, can be analysed simultaneously.
    DOI:
    10.1002/omr.1270210609
  • 作为产物:
    描述:
    3-丁基-环戊酮1,4-dihydronicotinamide adenine dinucleotide 、 horse liver alcohol dehydrogenase 作用下, 以 乙醇 为溶剂, 生成 (1S,3R)-3-Ethyl-cyclopentanol 、 (1R,3S)-3-n-butylcyclopentanol
    参考文献:
    名称:
    Use of shift reagent with MTPA derivatives in19F NMR spectrocopy: IV—Determination of enantiomeric composition for a variety of secondary cycloalkanols. A survey
    摘要:
    AbstractChiral secondary cycloalkanols (monocyclic alcohols) are derivatized to the corresponding (R)‐α‐methoxy‐α‐trifluoromethyl‐α‐phenylacetic acid [(R)‐MTPA] esters and analysed by 19F NMR in the presence of tris(6,6,7,7,8,8,8‐heptafluoro‐2,2‐dimethyl‐3,5‐octanedionato) europium(III) [Eu(fod)3]. Using this method the enantiomeric composition can be measured for several cyclopentanols, cyclohexanols and cycloheptanols, with a variety of substitution patterns. It is shown that a mixture of four stereoisomeric cycloalkanols, such as cis and trans disubstituted alcohols, can be analysed simultaneously.
    DOI:
    10.1002/omr.1270210609
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文献信息

  • Hepatitis C Virus Inhibitors
    申请人:Belema Makonen
    公开号:US20110286961A1
    公开(公告)日:2011-11-24
    The present disclosure relates to compounds, compositions and methods for the treatment of Hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.
    本公开涉及化合物、组合物和治疗丙型肝炎病毒(HCV)感染的方法。还公开了含有这些化合物的制药组合物以及使用这些化合物治疗HCV感染的方法。
  • [EN] 2, 8-DIAZASPIRO [4.5] DECANE COMPOUNDS<br/>[FR] COMPOSÉS 2,8-DIAZASPIRO[4.5]DÉCANES
    申请人:GENENTECH INC
    公开号:WO2022253341A1
    公开(公告)日:2022-12-08
    Disclosed are 2, 8-diazaspiro [4.5] decane compounds, including (pyrido [3, 4-d] pyrimidin-4-yl) -2, 8-diazaspiro [4.5] decane compounds, (2, 6-naphthyridin-1-yl) -2, 8-diazaspiro [4.5] decane compounds, and (1, 7-naphthyridin-4-yl) -2, 8-diazaspiro [4.5] decane compounds, that are inhibitors of LATS1/2, compositions containing these compounds, and methods for inhibiting LATS1/2 activity.
    本发明涉及2,8-二氮杂螺[4.5]癸烷化合物,包括(吡啶并[3,4-d]嘧啶-4-基)-2,8-二氮杂螺[4.5]癸烷化合物,(2,6-萘啶基)-2,8-二氮杂螺[4.5]癸烷化合物,以及(1,7-萘啶基-4-基)-2,8-二氮杂螺[4.5]癸烷化合物,它们是LATS1/2的抑制剂,以及含有这些化合物的组合物和抑制LATS1/2活性的方法。
  • [EN] HETEROCYCLIC CETP INHIBITORS<br/>[FR] INHIBITEURS DE CETP HETEROCYCLIQUES
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2007062314A2
    公开(公告)日:2007-05-31
    [EN] Compounds of formula Ia and Ib wherein A, B, C and R1 are described herein.
    [FR] La présente invention concerne des composés de formules Ia et Ib dans lesquelles A, B, C et R1 ont les correspondances indiquées dans l'invention.
  • [EN] METABOLITES OF THE JANUS KINASE INHIBITOR (R)-3-(4-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-LH-PYRAZOL-L-YL)-3- CYCLOPENTYLPROPANENITRILE<br/>[FR] MÉTABOLITES DE L'INHIBITEUR DE JANUS KINASE (R)-3-(4-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-1H-PYRAZOL-1-YL)-3-CYCLOPENTYLPROPANENITRILE
    申请人:INCYTE CORP
    公开号:WO2008157207A2
    公开(公告)日:2008-12-24
    [EN] The present invention provides active metablites of 3-(4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.
    [FR] L'invention concerne des métabolites actifs de 3-(4-(7H-pyrrolo[2,3-D]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile qui modulent l'activité de Janus kinases et sont utiles dans le traitement des maladies relatives à l'activité de Janus kinases comprenant, par exemple, des maladies immunologiques, des affections cutanées, des troubles prolifératifs de myéloïde, des cancers, et d'autres maladies.
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