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3-氨基己烷-2-酮 | 732924-23-1

中文名称
3-氨基己烷-2-酮
中文别名
——
英文名称
3-amino-hexan-2-one
英文别名
Methyl-(α-amino-butyl)-keton;3-Amino-hexan-2-on;3-Amino-hexanon-2;3-Aminohexan-2-one
3-氨基己烷-2-酮化学式
CAS
732924-23-1
化学式
C6H13NO
mdl
——
分子量
115.175
InChiKey
JSSKKCFDEASHBK-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):
    0.3
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    43.1
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:4efeac66f5ef872e2bd2e7c2cc7e6c63
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反应信息

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文献信息

  • [EN] FUSED TRICYCLIC ARYL COMPOUNDS USEFUL FOR THE TREATMENT OF VIRAL DISEASES<br/>[FR] COMPOSÉS ARYLES TRICYCLIQUES CONDENSÉS UTILES POUR LE TRAITEMENT DE MALADIES VIRALES
    申请人:SCHERING CORP
    公开号:WO2010132538A1
    公开(公告)日:2010-11-18
    The present invention relates to novel Fused Tricyclic Aryl Compounds, compositions comprising at least one Fused Tricyclic Aryl Compound, and methods of using the Fused Tricyclic Aryl Compounds for treating or preventing HCV infection in a patient.
    本发明涉及新型融合三环芳基化合物、包含至少一种融合三环芳基化合物的组合物,以及使用这些融合三环芳基化合物治疗或预防患者中HCV感染的方法。
  • [EN] ANTIVIRAL COMPOUNDS COMPOSED OF THREE LINKED ARYL MOIETIES TO TREAT DISEASES SUCH AS HEPATITIS C<br/>[FR] COMPOSÉS ANTIVIRAUX DE TROIS FRACTIONS D'ARYLE LIÉES POUR TRAITER DES MALADIES TELLES QUE L'HÉPATITE C
    申请人:SCHERING CORP
    公开号:WO2010138791A1
    公开(公告)日:2010-12-02
    The present invention relates to novel Linked Tricyclic Aryl Compounds, compositions comprising at least one Linked Tricyclic Compound, and methods of using Linked Tricyclic Aryl Compounds for treating or preventing HCV infection in a patient. in one aspect, the present invention provides Compounds of Formula (I): and pharmaceutically acceptable salts thereof, wherein: Non-limiting examples of the Compounds of Formula (II) include compound 56
    本发明涉及新型联苯三环化合物,包含至少一种联苯三环化合物的组合物,以及利用联苯三环化合物治疗或预防患者HCV感染的方法。在一个方面,本发明提供了式(I)的化合物及其药用盐,其中:式(II)的化合物的非限制性示例包括化合物56。
  • Process for Preparing Optically Active Aminopentane Derivative, Intermediate and Process for Preparing Intermediate
    申请人:Yoneda Fumio
    公开号:US20090124813A1
    公开(公告)日:2009-05-14
    There are provided a process for preparing an optically active aminopentane derivative that is promising as a psychotropic agent, an antidepressant agent, an antiparkinsonian agent, an anti-Alzheimer's agent, an apoptosis inhibitor, or the like; a novel optically active intermediate oxathiazolidine derivative very useful in the production of the aminopentane derivative; and process for the production thereof. The optically active aminopentane derivatives can be produced in an industrially advantageous manner from a novel optically active oxathiazolidine derivative represented by formula (5): wherein * indicates the position of an asymmetric carbon atom in the R or S configuration, and n is 0 or 1.
    提供了一种制备光学活性戊烷生物的方法,该衍生物可作为精神药物、抗抑郁药物、抗帕森病药物、抗阿尔茨海默病药物、凋亡抑制剂等,一种新型光学活性中间体噁嗪硫脲环衍生物,非常有用于制备戊烷生物;以及其生产方法。光学活性戊烷生物可以从新型光学活性噁嗪硫脲环衍生物中工业上优势地生产,该噁嗪硫脲环衍生物化学式表示为(5):其中*表示R或S构型的不对称碳原子的位置,n为0或1。
  • SUBSTITUTED ISOQUINOLINEAND ISOQUINOLINONE DERIVATIVES
    申请人:Plettenburg Oliver
    公开号:US20120316152A1
    公开(公告)日:2012-12-13
    A method for the treatment or prevention in a mammal of a disease associated with Rho-kinase and/or Rho-kinase mediated phosphorylation of myosin light chain phosphatase comprising administering to the mammal in need thereof at least one compound of the formula (I)
    一种用于治疗或预防哺乳动物中与Rho-激酶和/或Rho-激酶介导的肌球蛋白轻链磷酸磷酸化相关的疾病的方法,包括向需要该方法的哺乳动物中至少给予一个式(I)的化合物。
  • PROCESS FOR PREPARING OPTICALLY ACTIVE AMINOPENTANE DERIVATIVE, INTERMEDIATE AND PROCESS FOR PREPARING INTERMEDIATE
    申请人:Yoneda Fumio
    公开号:US20100324300A1
    公开(公告)日:2010-12-23
    There are provided a process for preparing an optically active aminopentane derivative that is promising as a psychotropic agent, an antidepressant agent, an antiparkinsonian agent, an anti-Alzheimer's agent, an apoptosis inhibitor, or the like; a novel optically active intermediate oxathiazolidine derivative very useful in the production of the aminopentane derivative; and process for the production thereof. The optically active aminopentane derivatives can be produced in an industrially advantageous manner from a novel optically active oxathiazolidine derivative represented by formula (5): wherein * indicates the position of an asymmetric carbon atom in the R or S configuration, and n is 0 or 1.
    提供一种制备具有潜在作为精神药物、抗抑郁药、抗帕森病药物、抗阿尔茨海默病药物、凋亡抑制剂等作用的光学活性戊烷生物的方法;一种非常有用于戊烷生物生产的新型光学活性内酰胺噻唑环衍生物;以及其生产方法。这些光学活性戊烷生物可以从由式(5)表示的新型光学活性内酰胺噻唑环衍生物中以工业上的有利方式生产出来:其中*表示R或S构型的不对称碳原子的位置,n为0或1。
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