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8-fluoro-4-methyl-2H-chromen-2-one | 1155195-30-4

中文名称
——
中文别名
——
英文名称
8-fluoro-4-methyl-2H-chromen-2-one
英文别名
8-fluoro-4-methylcoumarin;8-Fluoro-4-methylchromen-2-one
8-fluoro-4-methyl-2H-chromen-2-one化学式
CAS
1155195-30-4
化学式
C10H7FO2
mdl
——
分子量
178.163
InChiKey
WABSJCRBTNVLDD-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:
    297.5±35.0 °C(Predicted)
  • 密度:
    1.279±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    8-fluoro-4-methyl-2H-chromen-2-oneN-溴代丁二酰亚胺(NBS)偶氮二异丁腈 作用下, 以 四氯化碳二甲基亚砜 为溶剂, 反应 19.0h, 生成 4-((3-chlorophenylamino)methyl)-8-fluoro-2H-chromen-2-one
    参考文献:
    名称:
    Discovery of Inducible Nitric Oxide Synthase (iNOS) Inhibitor Development Candidate KD7332, Part 1: Identification of a Novel, Potent, and Selective Series of Quinolinone iNOS Dimerization Inhibitors that are Orally Active in Rodent Pain Models
    摘要:
    There are three isoforms of dimeric nitric oxide synthases (NOS) that convert arginine to citrulline and nitric oxide. Inducible NOS is implicated in numerous inflammatory diseases and, mote recently, in neuropathic pain states. The majority of existing NOS inhibitors are either based on the structure of arginine or are substrate competitive. We describe the identification from an ultra high-throughput screen of a novel series of quinolinone small molecule, nonarginine iNOS dimerization inhibitors. SAR studies on the screening hit, coupled with an in vivo lipopolysaccharide (LPS) challenge assay measuring plasma nitrates and drug levels, rapidly led to the identification of compounds 12 and 42-potent inhibitors of the human and mouse iNOS enzyme that were highly selective over endothelial NOS (eNOS). Following oral dosing, compounds 12 and 42 gave a statistical reduction in pain behaviors in the mouse formalin model, while 12 also statistically reduced neuropathic pain behaviors in the chronic constriction injury (Bennett) model.
    DOI:
    10.1021/jm900173b
  • 作为产物:
    描述:
    2-丁炔酸2-氟苯酚ytterbium(III) triflate hydrate 作用下, 反应 0.03h, 以94%的产率得到8-fluoro-4-methyl-2H-chromen-2-one
    参考文献:
    名称:
    三氟乙磺酸promote促进酚与丙酸的偶联:香豆素的合成
    摘要:
    香豆素是众所周知的天然和半合成产品,具有重要的有效药理活性。在这封信中,描述了一种化学合成这类化合物的改进方法。在10%的Yb(OTf)3水合物作为催化剂存在下,在短时间内从微波辐射和无溶剂条件下,短短地从不同取代的酚和丙酸作为起始原料,以良好的产率获得了香豆素。
    DOI:
    10.1016/j.tetlet.2016.05.087
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文献信息

  • SELF-CONTAINED BIOLOGICAL INDICATOR
    申请人:3M Innovative Properties Co.
    公开号:EP3829658A1
    公开(公告)日:2021-06-09
  • [EN] SELF-CONTAINED BIOLOGICAL INDICATOR<br/>[FR] INDICATEUR BIOLOGIQUE AUTONOME
    申请人:3M INNOVATIVE PROPERTIES CO
    公开号:WO2020023833A1
    公开(公告)日:2020-01-30
    The present disclosure is directed to self-contained biological indicators wherein a single type of indicator is capable of being used for various sterilization conditions, including sterilization with steam and/or ethylene oxide. In some embodiments, a single type of biological indicator is capable of being used for different steam sterilization conditions having varied temperatures and sterilization cycles.
  • [EN] SELF-CONTAINED BIOLOGICAL INDICATOR WITH SALT COMPOUND<br/>[FR] INDICATEUR BIOLOGIQUE AUTONOME AVEC COMPOSÉ SALIN
    申请人:3M INNOVATIVE PROPERTIES CO
    公开号:WO2021148909A1
    公开(公告)日:2021-07-29
    The present disclosure is directed to self-contained biological indicators wherein a single type of indicator is capable of being used for various sterilization conditions, including sterilization with steam, hydrogen peroxide, and/or ethylene oxide. In some embodiments, a single type of biological indicator is capable of being used for different steam sterilization conditions having varied temperatures and sterilization cycles.
  • Discovery of Inducible Nitric Oxide Synthase (iNOS) Inhibitor Development Candidate KD7332, Part 1: Identification of a Novel, Potent, and Selective Series of Quinolinone iNOS Dimerization Inhibitors that are Orally Active in Rodent Pain Models
    作者:Céline Bonnefous、Joseph E. Payne、Jeffrey Roppe、Hui Zhuang、Xiaohong Chen、Kent T. Symons、Phan M. Nguyen、Marciano Sablad、Natasha Rozenkrants、Yan Zhang、Li Wang、Daniel Severance、John P. Walsh、Nahid Yazdani、Andrew K. Shiau、Stewart A. Noble、Peter Rix、Tadimeti S. Rao、Christian A. Hassig、Nicholas D. Smith
    DOI:10.1021/jm900173b
    日期:2009.5.14
    There are three isoforms of dimeric nitric oxide synthases (NOS) that convert arginine to citrulline and nitric oxide. Inducible NOS is implicated in numerous inflammatory diseases and, mote recently, in neuropathic pain states. The majority of existing NOS inhibitors are either based on the structure of arginine or are substrate competitive. We describe the identification from an ultra high-throughput screen of a novel series of quinolinone small molecule, nonarginine iNOS dimerization inhibitors. SAR studies on the screening hit, coupled with an in vivo lipopolysaccharide (LPS) challenge assay measuring plasma nitrates and drug levels, rapidly led to the identification of compounds 12 and 42-potent inhibitors of the human and mouse iNOS enzyme that were highly selective over endothelial NOS (eNOS). Following oral dosing, compounds 12 and 42 gave a statistical reduction in pain behaviors in the mouse formalin model, while 12 also statistically reduced neuropathic pain behaviors in the chronic constriction injury (Bennett) model.
  • Ytterbium triflate promoted coupling of phenols and propiolic acids: synthesis of coumarins
    作者:Serena Fiorito、Francesco Epifano、Vito A. Taddeo、Salvatore Genovese
    DOI:10.1016/j.tetlet.2016.05.087
    日期:2016.6
    Coumarins are a well-known class of natural occurring and semi-synthetic products with reported important and effective pharmacological activities. In this Letter an improved method for the chemical synthesis of such compounds is described. Coumarins have been obtained in good to excellent yields under microwave irradiation and solvent-free conditions in a short time from differently substituted phenols
    香豆素是众所周知的天然和半合成产品,具有重要的有效药理活性。在这封信中,描述了一种化学合成这类化合物的改进方法。在10%的Yb(OTf)3水合物作为催化剂存在下,在短时间内从微波辐射和无溶剂条件下,短短地从不同取代的酚和丙酸作为起始原料,以良好的产率获得了香豆素。
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