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5-(3-fluorophenoxy)thiophene-2-carbonitrile | 849806-06-0

中文名称
——
中文别名
——
英文名称
5-(3-fluorophenoxy)thiophene-2-carbonitrile
英文别名
——
5-(3-fluorophenoxy)thiophene-2-carbonitrile化学式
CAS
849806-06-0
化学式
C11H6FNOS
mdl
——
分子量
219.239
InChiKey
MHLYRVZYNRASBD-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:
    314.5±37.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    61.3
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    描述:
    5-(3-fluorophenoxy)thiophene-2-carbonitrile 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 以81%的产率得到C-(5-(3-fluorophenoxy)thiophen-2-yl)methylamine
    参考文献:
    名称:
    Synthesis and evaluation of novel antifungal agents-quinoline and pyridine amide derivatives
    摘要:
    Quinoline amide, azaindole amide and pyridine amides were synthesized and tested for in vitro antifungal activity against fungi. These synthesized amides have potent antifungal activity against Candida albicans and Aspergillus fumigatus. Our results suggest that hetero ring amides may be potent antifungal agents that operate by inhibiting the function of Gwt1 protein in the GPI biosynthetic pathway. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.06.005
  • 作为产物:
    描述:
    5-硝基噻酚-2-甲腈3-氟苯酚potassium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 16.0h, 以23.5%的产率得到5-(3-fluorophenoxy)thiophene-2-carbonitrile
    参考文献:
    名称:
    EP1669348
    摘要:
    公开号:
点击查看最新优质反应信息

文献信息

  • Novel antifungal agent containing heterocyclic compound
    申请人:Nakamoto Kazutaka
    公开号:US20070105943A1
    公开(公告)日:2007-05-10
    The present invention provides an antifungal agent represented by the formula: [wherein A 1 represents a 3-pyridyl group which may have a substituent, a quinolyl group which may have a substituent, or the like; X 1 represents a group represented by the formula —NH—C(═O)—, a group represented by the formula —C(═O)—NH—, or the like; E represents a furyl group, a thienyl group, a pyrrolyl group, a phenyl group, a pyridyl group, a tetrazolyl group, a thiazolyl group or a pyrazolyl group; with the proviso that A 1 may have 1 to 3 substituents, and E has one or two substituents].
    本发明提供了一种抗真菌剂,其表示为以下式子: [其中A1表示一个3-吡啶基团,可能具有取代基,喹啉基团,可能具有取代基或类似物;X1表示由公式—NH—C(═O)—,由公式—C(═O)—NH—或类似物表示的基团;E表示呋喃基团,噻吩基团,吡咯基团,苯基团,吡啶基团,四唑基团,噻唑基团或吡唑基团;但A1可能具有1到3个取代基,E具有一个或两个取代基。]
  • Novel Antimalarial Agent Containing Heterocyclic Compound
    申请人:Nakamoto Kazutaka
    公开号:US20090227799A1
    公开(公告)日:2009-09-10
    Disclosed is an antimalarial agent containing a compound represented by the formula: [wherein A 1 represents a 3-pyridyl group that may have a substituent, a 6-quinolyl group that may have a substituent, or the like; X 1 represents a group represented by the formula —C(═O)—NH— or the like; E represents a furyl group, a thienyl group or a phenyl group; with the proviso that A 1 may have one to three substituents, and E has one of two substituents] or a salt thereof or hydrates thereof.
    揭示了一种抗疟疾剂,其包含由下式表示的化合物: [其中A1表示一个3-吡啶基团,可以有取代基,一个6-喹啉基团,可以有取代基或类似物;X1表示一个由公式-C(═O)-NH-或类似物表示的基团;E表示一个呋喃基团,噻吩基团或苯基团;但前提是A1可以有1到3个取代基,E有两个取代基之一]或其盐或水合物。
  • NOVEL ANTIFUNGAL AGENT CONTAINING HETEROCYCLIC COMPOUND
    申请人:NAKAMOTO Kazutaka
    公开号:US20110195999A1
    公开(公告)日:2011-08-11
    The present invention provides an antifungal agent represented by the formula: wherein A 1 represents a 3-pyridyl group which may have a substituent, a quinolyl group which may have a substituent, or the like; X 1 represents a group represented by the formula —NH—C(═O)—, a group represented by the formula —C(═O)—NH—, or the like; E represents a furyl group, a thienyl group, a pyrrolyl group, a phenyl group, a pyridyl group, a tetrazolyl group, a thiazolyl group or a pyrazolyl group; with the proviso that A 1 may have 1 to 3 substituents, and E has one or two substituents.
    本发明提供一种抗真菌剂,其化学式如下: 其中,A1代表3-吡啶基,可以有取代基,喹啉基,也可以有取代基等;X1代表由公式—NH—C(═O)—,由公式—C(═O)—NH—等表示的基团;E代表呋喃基,噻吩基,吡咯基,苯基,吡啶基,四唑基,噻唑基或吡唑基;但要求A1可能有1到3个取代基,E有1或2个取代基。
  • Antifungal agent containing heterocyclic compound
    申请人:Eisai R&D Management Co., Ltd.
    公开号:US07932272B2
    公开(公告)日:2011-04-26
    The present invention provides an antifungal agent represented by the formula: [wherein A1 represents a 3-pyridyl group which may have a substituent, a quinolyl group which may have a substituent, or the like; X1 represents a group represented by the formula —NH—C(═O)—, a group represented by the formula —C(═O)—NH—, or the like; E represents a furyl group, a thienyl group, a pyrrolyl group, a phenyl group, a pyridyl group, a tetrazolyl group, a thiazolyl group or a pyrazolyl group; with the proviso that A1 may have 1 to 3 substituents, and E has one or two substituents].
    本发明提供了一种抗真菌剂,其化学式如下:[其中A1代表3-吡啶基,可以具有取代基,喹啉基,也可以具有取代基等;X1代表由公式—NH—C(═O)—,由公式—C(═O)—NH—等表示的基团;E代表呋喃基,噻吩基,吡咯基,苯基,吡啶基,四唑基,噻唑基或吡唑基;限制条件是A1可以有1到3个取代基,E有一个或两个取代基]。
  • NOVEL ANTIFUNGAL AGENT COMPRISING HETEROCYCLIC COMPOUND
    申请人:Eisai Co., Ltd.
    公开号:EP1669348A1
    公开(公告)日:2006-06-14
    The present invention provides an antifungal agent represented by the formula: [wherein A1 represents a 3-pyridyl group which may have a substituent, a quinolyl group which may have a substituent, or the like; X1 represents a group represented by the formula -NH-C(=O)-, a group represented by the formula -C(=O)-NH-, or the like; E represents a furyl group, a thienyl group, a pyrrolyl group, a phenyl group, a pyridyl group, a tetrazolyl group, a thiazolyl group or a pyrazolyl group; with the proviso that A1 may have 1 to 3 substituents, and E has one or two substituents].
    本发明提供了一种由式表示的抗真菌剂: [其中A1代表可具有取代基的3-吡啶基、可具有取代基的喹啉基或类似基团;X1代表由式-NH-C(=O)-代表的基团、由式-C(=O)-NH-代表的基团或类似基团;E 代表呋喃基、噻吩基、吡咯基、苯基、吡啶基、四唑基、噻唑基或吡唑基;但 A1 可具有 1 至 3 个取代基,E 具有 1 或 2 个取代基]。
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