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2-methyl-hexane-3,4-dione | 51945-99-4

中文名称
——
中文别名
——
英文名称
2-methyl-hexane-3,4-dione
英文别名
2-Methylhexane-3,4-dione
2-methyl-hexane-3,4-dione化学式
CAS
51945-99-4
化学式
C7H12O2
mdl
——
分子量
128.171
InChiKey
VYDFLMCRLHTTEX-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):
    1.1
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-methyl-hexane-3,4-dione4,5-二氟苯-1,2-二胺乙醇 为溶剂, 以69%的产率得到6,7-Difluoro-3-isopropyl-2(1H)-quinoxalinone
    参考文献:
    名称:
    Preparation and biological evaluation of 6/7-trifluoromethyl(nitro)-, 6,7-difluoro-3-alkyl (aryl)-substituted-quinoxalin-2-ones. Part 3
    摘要:
    A new series of quinoxalinones 6/7-trifluoromethyl or nitro- and 6,7-difluoro substituted bearing various side-chains (alkyl, halogenoalkyl, benzyl and phenyl groups) at C-3 of the ring system was synthesized and submitted to preliminary in vitro evaluation for antibacterial, antifungal, antimycobacterial, anticancer and anti-HIV activities. Results of these screenings showed that compounds 23-28 exhibited a good inhibition activity against various strains of Candida. Compound 24 showed also an interesting in vitro anticancer activity. (C) 1999 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(99)00011-7
  • 作为产物:
    参考文献:
    名称:
    Dedieu,M.; Pascal,Y.-L., Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1974, vol. 278, p. 9 - 11
    摘要:
    DOI:
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文献信息

  • Compositions and Methods for Fermentation of Biomass
    申请人:Parekh Sarad
    公开号:US20100268000A1
    公开(公告)日:2010-10-21
    In one aspect, this invention relates to production of useful fermentation end-products from biomass through simultaneous hydrolysis and fermentation by a microorganism, such as Clostridium phytofermentans . The invention also relates to the development of a process for efficient pretreatment and conversion of lignocellulosic biomass to end-products with high conversion efficiency (yield). In another aspect, methods for producing a fermentation end-product by fermenting hexose (C6) and pentose (C5) sugars with a microorganism, such as Clostridium phytofermentans are disclosed herein.
    在一个方面,这项发明涉及通过微生物(如植物发酵槽菌)的同时水解和发酵,从生物质中生产有用的发酵终产物。该发明还涉及开发一种高效预处理和转化木质纤维素生物质为高转化效率(产率)的终产物的过程。在另一个方面,本文介绍了利用微生物(如植物发酵槽菌)发酵己糖(C6)和戊糖(C5)糖产生发酵终产物的方法。
  • BIOFUEL PRODUCTION
    申请人:Yoshikuni Yasuo
    公开号:US20090139134A1
    公开(公告)日:2009-06-04
    Methods, enzymes, recombinant microorganism, and microbial systems are provided for converting polysaccharides, such as those derived from biomass, into suitable monosaccharides or oligosaccharides, as well as for converting suitable monosaccharides or oligosaccharides into commodity chemicals, such as biofuels. Commodity chemicals produced by the methods described herein are also provided. Commodity chemical enriched, refinery-produced petroleum products are also provided, as well as methods for producing the same.
    提供了用于将多糖转化为适当的单糖或寡糖的方法、酶、重组微生物和微生物系统,例如从生物质中提取的多糖。同时提供了将适当的单糖或寡糖转化为商品化学品,如生物燃料的方法。本文描述的方法生产的商品化学品也提供了。此外,还提供了商品化学品富集的、精炼生产的石油产品,以及生产这些产品的方法。
  • Inhibitors of serine proteases, particular HCV NS3-NS4A protease
    申请人:Pitlik Janos
    公开号:US20070292933A1
    公开(公告)日:2007-12-20
    The present invention relates to compounds that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention. The invention further relates to processes for preparing these compounds.
    本发明涉及抑制丝氨酸蛋白酶活性的化合物,特别是乙型肝炎病毒NS3-NS4A蛋白酶的活性。因此,它们通过干扰乙型肝炎病毒的生命周期而起作用,并且也可用作抗病毒剂。本发明还涉及包含这些化合物的组合物,无论是用于体外使用还是用于治疗患有HCV感染的患者的给药。本发明还涉及通过给予含有本发明化合物的组合物来治疗患有HCV感染的患者的方法。本发明还涉及制备这些化合物的过程。
  • METHODS AND COMPOSITIONS FOR PRODUCING CHEMICAL PRODUCTS FROM C. PHYTOFERMENTANS
    申请人:Schmalisch Matthias
    公开号:US20110183382A1
    公开(公告)日:2011-07-28
    This invention provides systems and methods for the production of compounds by C. phytofermentans. C. phytofermentans is genetically-engineered for hydrolysis and fermentation of carbonaceous biomass to synthesize compounds of commercial value.
    这项发明提供了通过C. phytofermentans生产化合物的系统和方法。C. phytofermentans被基因工程化,用于水解和发酵碳质生物质以合成具有商业价值的化合物。
  • INHIBITORS OF SERINE PROTEASES, PARTICULARLY HCV NS3-NS4A PROTEASE
    申请人:Pitlik Janos
    公开号:US20100173851A1
    公开(公告)日:2010-07-08
    The present invention relates to compounds that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention. The invention further relates to processes for preparing these compounds.
    本发明涉及抑制丝氨酸蛋白酶活性,特别是丙型肝炎病毒NS3-NS4A蛋白酶活性的化合物。因此,它们通过干扰丙型肝炎病毒的生命周期发挥作用,并且也可用作抗病毒剂。本发明还涉及包含这些化合物的组合物,无论是用于体外使用还是用于治疗HCV感染的患者的给药。本发明还涉及通过给予含有本发明化合物的组合物来治疗患者的HCV感染的方法。本发明还涉及制备这些化合物的方法。
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