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7,7-dimethyl-4-octanone

中文名称
——
中文别名
——
英文名称
7,7-dimethyl-4-octanone
英文别名
7,7-Dimethyloctan-4-one
7,7-dimethyl-4-octanone化学式
CAS
——
化学式
C10H20O
mdl
——
分子量
156.268
InChiKey
ASQGMZXLJJHPPL-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):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    3,3-二甲基-1-丁烯十二羰基三钌 盐酸 作用下, 以 甲苯 为溶剂, 反应 6.0h, 生成 7,7-dimethyl-4-octanone
    参考文献:
    名称:
    Catalytic Activation of C−H and C−C Bonds of Allylamines via Olefin Isomerization by Transition Metal Complexes
    摘要:
    The metal-catalyzed reaction of olefins with allylamines bearing coordination sites (2-pyridyl groups) was studied. With Ru-3(CO)(12) as catalyst, activation of C-H bonds led to the formation of ketimines that were hydrolyzed to give asymmetric ketones. With [(C8H14)(2)RhCl](2), both C-H and C-C bonds were activated and symmetric ketones were formed on hydrolysis. The reaction involves double bond migration of the allylamine to form an aldimine.
    DOI:
    10.1021/ol990357b
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文献信息

  • TRICYCLIC HETEROCYCLIC COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF
    申请人:Babu Srinivasan
    公开号:US20110201593A1
    公开(公告)日:2011-08-18
    The invention provides novel compounds of formula I having the general formula: wherein R 1 , R 2 , R 3 , X and Y are as described herein. Accordingly, the compounds may be provided in pharmaceutically acceptable compositions and used for the treatment of immunological or hyperproliferative disorders.
    本发明提供了具有以下一般式的新化合物I: 其中R1、R2、R3、X和Y如本文所述。因此,这些化合物可以在药学上可接受的组合物中提供,并用于治疗免疫或过度增生性疾病。
  • 5-PHENYL-4-METHYL-THIAZOL-2-YL-AMINE DERIVATIVES AS INHIBITORS OF PHOSPHATIDYLINOSITOL 3 KINASE ENZYMES (PI3) FOR THE TREATMENT OF INFLAMMATORY DISEASES
    申请人:Bloomfield Graham Charles
    公开号:US20110124624A1
    公开(公告)日:2011-05-26
    Compounds of Formula I: in free or salt form, wherein R a , R b , R 2 , R 3 , R 4 and R 5 have the meanings as indicated in the specification, are useful for treating conditions that are mediated by phosphatidylinositol 3-kinase. Pharmaceutical compositions that contain the compounds and a process for preparing the compounds are also described.
    公式I的化合物:以自由或盐形式存在,其中Ra、Rb、R2、R3、R4和R5的含义如规范中所示,可用于治疗由磷脂酰肌醇3-激酶介导的疾病。还描述了含有这些化合物的制药组合物和制备这些化合物的过程。
  • NOVEL ANTIMICROBIALS
    申请人:Jain Rajesh
    公开号:US20110245258A1
    公开(公告)日:2011-10-06
    The present invention relates to novel phenyl oxazolidinone compounds of formula I, their pharmaceutically acceptable analogs, tautomeric forms, stereoisomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The invention also relates to the processes for the synthesis of novel compounds of formula I or their pharmaceutically acceptable analogs, tautomeric forms, stereoisomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The present invention also provides pharmaceutical compositions comprising novel compounds of formula I and methods of using them. The compounds of the present invention are useful as antimicrobial agents, effective against a number of aerobic and/or anaerobic Gram positive and/or Gram negative pathogens such as multi drug resistant species of Staphylococcus, Streptococcus, Enterococcus, Bacterioides, Clostridia, H. influenza, Moraxella, acid-fast organisms such as Mycobacterium tuberculosis as well as Linezolid resistant species of Staphylococcus and Enterococcus.
    本发明涉及公式I的新型苯基噁唑啉酮化合物,它们的药学上可接受的类似物、互变异构体、立体异构体、多晶形态、前药、代谢物、盐或其溶剂。本发明还涉及合成公式I的新化合物或其药学上可接受的类似物、互变异构体、立体异构体、多晶形态、前药、代谢物、盐或其溶剂的过程。本发明还提供了包含公式I的新化合物的制药组合物和使用它们的方法。本发明的化合物是抗微生物剂,对多种需氧和/或厌氧革兰阳性和/或革兰阴性病原体具有有效作用,如金黄色葡萄球菌、链球菌、肠球菌、拟杆菌、梭菌、流感嗜血杆菌、摩拉克斯氏菌、抗利多霉素的金黄色葡萄球菌和肠球菌等耐药菌。
  • AURISTATIN COMPOUNDS AND CONJUGATES THEREOF
    申请人:MERSANA THERAPEUTICS, INC.
    公开号:US20150314008A1
    公开(公告)日:2015-11-05
    An auristatin compound conjugate is provided herein. The conjugate comprises a protein based recognition-molecule (PBRM) and a polymeric carrier substituted with one or more -L D -D, the protein based recognition-molecule being connected to the polymeric carrier by L p . Each occurrence of D is independently an auristatin compound having a molecular weight ≦5 kDa. L D and L p are distinct linkers connecting the auristatin compound and PBRM to the polymeric earner respectively. Also disclosed are polymeric scaffolds useful for conjugating with a PBRM to form a polymer-auristatin compound-PBRM conjugate described herein, compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions.
    本文提供了一种auristatin化合物结合物。该结合物包括以蛋白质为基础的识别分子(PBRM)和多聚载体,该多聚载体被取代了一个或多个-LD-D,蛋白质基础的识别分子通过Lp连接到多聚载体上。每个D的出现都是独立的,具有分子量≦5 kDa的auristatin化合物。 LD和Lp是连接auristatin化合物和PBRM到多聚载体的不同连接物。还公开了用于与PBRM共轭形成在此处描述的聚合物-auristatin化合物-PBRM结合物的聚合物支架,包括结合物的组成,其制备方法以及使用结合物或其组成治疗各种疾病的方法。
  • THERMAL TRANSFER INK SHEET, INK CARTRIDGE, COATING COMPOSITION FOR DYE LAYER OF THERMAL TRANSFER INK SHEET, AND THERMAL TRANSFER RECORDING METHOD
    申请人:YOSHIZAWA Masataka
    公开号:US20080242540A1
    公开(公告)日:2008-10-02
    A thermal transfer ink sheet comprising, as formed on a support, a dye layer containing a thermal transferable dye in a resin binder, wherein the dye layer contains a polyvinyl acetal modified with at least one compound of the following formula [1]: wherein one of R 1 and R 2 is a branched hydrocarbon group and the other is a hydrogen atom or a hydrocarbon group, or R 1 and R 2 are groups that bond to each other to form a cyclic hydrocarbon.
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