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trans-3-Isopropyl-cyclobutanol | 16453-25-1

中文名称
——
中文别名
——
英文名称
trans-3-Isopropyl-cyclobutanol
英文别名
——
trans-3-Isopropyl-cyclobutanol化学式
CAS
16453-25-1
化学式
C7H14O
mdl
——
分子量
114.188
InChiKey
SKKCZMZCVUZWCT-LJGSYFOKSA-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):
    1.41
  • 重原子数:
    8.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.23
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    trans-3-Isopropyl-cyclobutanol4-溴苯磺酰氯吡啶 作用下, 生成 trans-3-Isopropyl-cyclobutyl-brosylat
    参考文献:
    名称:
    Steric factors in the cationic rearrangement of substituted cyclobutanes
    摘要:
    DOI:
    10.1021/ja00736a020
  • 作为产物:
    描述:
    3-异丙基-环丁基胺高氯酸 、 sodium nitrite 作用下, 生成 trans-3-Isopropyl-cyclobutanol
    参考文献:
    名称:
    Nonplanar cyclobutane. Evidence for a conformationally controlled, classic mechanism in the deamination of cis- and trans-3-isopropylcyclobutylamine
    摘要:
    DOI:
    10.1021/jo01274a033
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文献信息

  • JANUS KINASE INHIBITOR COMPOUNDS AND METHODS
    申请人:GOODACRE SIMON CHARLES
    公开号:US20100317643A1
    公开(公告)日:2010-12-16
    The invention provides compounds of Formula I, stereoisomers or pharmaceutically acceptable salts thereof, wherein A, B, D, R 1 , R 2 , R 4 and R 5 are defined herein, a pharmaceutical composition that includes a compound of Formula I and methods of use thereof
    这项发明提供了公式I的化合物,其立体异构体或药学上可接受的盐,其中A、B、D、R1、R2、R4和R5在此处被定义,包括公式I化合物的药物组合物以及其使用方法
  • SPIRO-OXINDOLE MDM2 ANTAGONISTS
    申请人:Wang Shaomeng
    公开号:US20120122947A1
    公开(公告)日:2012-05-17
    Provided herein are compounds, compositions, and methods in the field of medicinal chemistry. The compounds and compositions provided herein relate to spiro-oxindoles which function as antagonists of the interaction between p53 and MDM2, and their use as therapeutics for the treatment of cancer and other diseases.
    本文提供了关于药物化学领域的化合物、组合物和方法。这里提供的化合物和组合物涉及螺环氧吲哚,其作为p53和MDM2相互作用的拮抗剂,并且它们作为治疗癌症和其他疾病的药物的用途。
  • ETHER DERIVATIVES OF BICYCLIC HETEROARYLS
    申请人:Chen Bei
    公开号:US20120165310A1
    公开(公告)日:2012-06-28
    The invention relates to compounds of formula I, wherein the substituents are as defined in the specification; to processes for the preparation of such compounds; pharmaceutical compositions comprising such compounds; such compounds as a medicament; such compounds for the treatment of a proliferative disease.
    本发明涉及式I的化合物,其中取代基如规范中所定义;制备此类化合物的方法;包含此类化合物的制药组合物;此类化合物作为药物;此类化合物用于治疗增生性疾病。
  • Benzene-fused 6-membered oxygen-containing heterocyclic derivatives of bicyclic heteroaryls
    申请人:Chen Bei
    公开号:US20120289501A1
    公开(公告)日:2012-11-15
    The invention relates to new derivatives of formula I, wherein the substituents are as defined in the specification; to processes for the preparation of such derivatives; pharmaceutical compositions comprising such derivatives; such derivatives as a medicament; such derivatives for the treatment of a proliferative disease.
    本发明涉及I式的新衍生物,其中取代基如规范中定义;制备这种衍生物的方法;包含这种衍生物的药物组合物;这种衍生物作为药物;这种衍生物用于治疗增生性疾病。
  • BIOMARKERS FOR MDM2 INHIBITORS FOR USE IN TREATING DISEASE
    申请人:Wang Shaomeng
    公开号:US20110251252A1
    公开(公告)日:2011-10-13
    Provided herein are methods for selecting and treating a subject with leukemia, wherein the subject is selected for treatment and is treated with an MDM2 inhibitor because said subject's cells contain an FLT3-ITD mutation.
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