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辛烷-2,4,6-三酮 | 61067-58-1

中文名称
辛烷-2,4,6-三酮
中文别名
——
英文名称
octane-2,4,6-trione
英文别名
——
辛烷-2,4,6-三酮化学式
CAS
61067-58-1
化学式
C8H12O3
mdl
——
分子量
156.181
InChiKey
KYWYXJJKXSANGZ-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

物化性质

  • 沸点:
    244.6±15.0 °C(Predicted)
  • 密度:
    1.027±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    51.2
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:9e32ce4b07279801f163199da21e98c9
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上下游信息

  • 下游产品
    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:
    参考文献:
    名称:
    Formation of trianions of 2,4,6-triketones. Synthesis of 3,5,7-triketo acids using lithium diisopropylamide
    摘要:
    DOI:
    10.1021/ja00440a047
  • 作为产物:
    参考文献:
    名称:
    Formation of trianions of 2,4,6-triketones. Synthesis of 3,5,7-triketo acids using lithium diisopropylamide
    摘要:
    DOI:
    10.1021/ja00440a047
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文献信息

  • BETULONIC AND BETULINIC ACID DERIVATIVES
    申请人:Leunis Jean-Claude
    公开号:US20090068257A1
    公开(公告)日:2009-03-12
    The present invention relates to betulonic and betulinic acid derivatives and, in particular, to C-28 and C-3 derivatives. The present invention relates to betulonic acid esters, dihydro-betulonic acid esters, PAG-modified betulinic acid derivatives, and PAG-modified dihydro-betulinic acid derivatives. Betulinic acid and derivatives thereof may be bound to a poly(alkylene glycol) (PAG) such as poly(ethylene glycol). Binding may be via a linker, such as a diamine, an amino acid, a peptide, an ester or a carbonate. The compounds of the present invention may be used for the treatment of cancer or a viral infection. The present invention also provides pharmaceutical compositions comprising the compounds of the present invention. The present invention further provides processes for the preparation of the compounds of the present invention, for example, from betulin.
    本发明涉及白桦酸和白桦皮酸衍生物,特别是C-28和C-3衍生物。本发明涉及白桦酸酯、二氢白桦酸酯、PAG修饰的白桦皮酸衍生物和PAG修饰的二氢白桦皮酸衍生物。白桦皮酸及其衍生物可以与聚(烯基氧化物)(PAG)如聚(乙二醇)结合。结合可以通过连接剂,例如二胺、氨基酸、肽、酯或碳酸酯实现。本发明的化合物可用于癌症或病毒感染的治疗。本发明还提供了包含本发明化合物的制药组合物。本发明还提供了制备本发明化合物的方法,例如从白桦中制备。
  • Acylations of Dilithio β-Diketones with Aliphatic Esters [ILL] Form 1,3,5-Triketones. Cyclizations to 4-Pyrones and 4-Pyridones
    作者:Stewart D. Work、Charles R. Hauser
    DOI:10.1021/jo01038a031
    日期:1963.3
  • COMPOSITION AND POLYMER
    申请人:Asahi Kasei Kabushiki Kaisha
    公开号:EP2735581B1
    公开(公告)日:2021-07-14
  • Immune Stimulatory Oligoribonucleotide Analogs Containing Modified Oligophosphate Moieties
    申请人:Debelak Harald
    公开号:US20100260788A1
    公开(公告)日:2010-10-14
    Immunostimulatory oligoribonucleotides (ORN) featuring 5′-triphosphates and various 5′-triphosphate analogs are provided. Also provided are physiologically acceptable salts of the immunostimulatory ORN and pharmaceutical compositions containing the immunostimulatory ORN of the invention. ORN of the invention are useful as adjuvants and can be combined with an antigen to promote an antigen-specific immune response. ORN of the invention are also particularly useful for promoting a Th1-type immune response. Also provided are methods of use of the compounds and pharmaceutical compositions of the invention to enhance an immune response in a subject, as well to treat a number of conditions including cancer, infection, allergy, and asthma, and to vaccinate a subject against an antigen.
  • IMMUNE STIMULATORY OLIGORIBONUCLEOTIDE ANALOGS CONTAINING MODIFIED OLIGOPHOSPHATE MOIETIES
    申请人:AdiuTide Pharmaceuticals GmbH
    公开号:US20130164333A1
    公开(公告)日:2013-06-27
    Immunostimulatory oligoribonucleotides (ORN) featuring 5′-triphosphates and various 5′-triphosphate analogs are provided. Also provided are physiologically acceptable salts of the immunostimulatory ORN and pharmaceutical compositions containing the immunostimulatory ORN of the invention. ORN of the invention are useful as adjuvants and can be combined with an antigen to promote an antigen-specific immune response. ORN of the invention are also particularly useful for promoting a Th1-type immune response. Also provided are methods of use of the compounds and pharmaceutical compositions of the invention to enhance an immune response in a subject, as well to treat a number of conditions including cancer, infection, allergy, and asthma, and to vaccinate a subject against an antigen.
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