摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5-氯-3-乙基苯并恶唑-2(3H)-酮 | 5790-91-0

中文名称
5-氯-3-乙基苯并恶唑-2(3H)-酮
中文别名
——
英文名称
5-chloro-3-ethylbenzo[d]oxazol-2(3H)-one
英文别名
5-chloro-3-ethyl-3H-benzooxazol-2-one;3-Ethyl-5-chlorobenzoxazolone;5-Chlor-2-oxo-3-aethyl-2.3-dihydro-benzoxazol;2-Benzoxazolinone, 5-chloro-3-ethyl-;5-chloro-3-ethyl-1,3-benzoxazol-2-one
5-氯-3-乙基苯并恶唑-2(3H)-酮化学式
CAS
5790-91-0
化学式
C9H8ClNO2
mdl
——
分子量
197.621
InChiKey
NGNSUTIRTDXXGA-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):
    2.5
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:648b156700b7f24984c5da6adf6c20f7
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    碘乙烷氯唑沙宗 反应 2.0h, 以98%的产率得到5-氯-3-乙基苯并恶唑-2(3H)-酮
    参考文献:
    名称:
    Electrogenerated N-heterocyclic carbenes: N-functionalization of benzoxazolones
    摘要:
    A simple electrochemical procedure for the N-acylation and N-alkylation of benzoxazol-2(3H)-ones has been set up via electrolysis of an ionic liquid containing a benzoxazolone followed by addition of saturated or unsaturated anhydrides or alkyl halides. The electrochemically induced N-functionalization of benzoxazol-2(3H)-ones works very well in all tested ionic liquids, avoiding the use of volatile organic solvents. The N-acyl and N-alkyl derivatives of benzoxazol-2(3H)-ones were isolated in good to excellent yields; moreover, the ionic liquid has been reused fivefold maintaining the high yield of the products. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.02.057
点击查看最新优质反应信息

文献信息

  • Benzimidazolone-, benzoxazolone-, or benzothiazolone derivatives as ion channel modulating agents
    申请人:——
    公开号:US20020055526A1
    公开(公告)日:2002-05-09
    The present invention relates to ion channel modulating agents. More particularly, the present invention relates to a particular class of chemical compounds that has proven useful as modulators of SK Ca , IK Ca and BK Ca channels. In further aspects, the present invention relates to the use of these SK/IK/BK channel modulating agents for the manufacture of medicaments, and pharmaceutical compositions comprising the SK/IK/BK channel modulating agents. The SK/IK/BK channel modulating agents of the invention are useful for the treatment or alleviation of diseases and conditions associated with the SK/IK/BK channels.
    本发明涉及离子通道调节剂。更具体地,本发明涉及一类特定的化合物,已被证明可作为SKCa、IKCa和BKCa通道的调节剂。此外,本发明还涉及利用这些SK/IK/BK通道调节剂制造药物,并包括这些SK/IK/BK通道调节剂的药物组合物。本发明的SK/IK/BK通道调节剂可用于治疗或缓解与SK/IK/BK通道相关的疾病和症状。
  • [EN] NEW BENZIMIDAZOLONE-, BENZOXAZOLONE-, OR BENZOTHIAZOLONE DERIVATIVES AS ION CHANNEL MODULATING AGENTS<br/>[FR] NOUVEAUX DERIVES DE BENZIMIDAZOLONE, DE BENZOXAZOLONE OU DE BENZOTHIAZOLONE AGISSANT COMME AGENTS DE MODULATION DE CANAUX IONIQUES
    申请人:NEUROSEARCH AS
    公开号:WO2000034248A1
    公开(公告)日:2000-06-15
    The present invention relates to ion channel modulating agents. More particularly, the present invention relates to a particular class of chemical compounds that has proven useful as modulators of SKCa, IKCa and BKCa channels. In further aspects, the present invention relates to the use of these SK/IK/BK channel modulating agents for the manufacture of medicaments, and pharmaceutical compositions comprising the SK/IK/BK channel modulating agents. The SK/IK/BK channel modulating agents of the invention are useful for the treatment or alleviation of diseases and conditions associated with the SK/IK/BK channels.
    本发明涉及离子通道调节剂。更具体地,本发明涉及一类已被证明可用作SKCa、IKCa和BKCa通道调节剂的化学化合物。在进一步的方面,本发明涉及使用这些SK/IK/BK通道调节剂制造药物,以及包含SK/IK/BK通道调节剂的制药组合物。本发明的SK/IK/BK通道调节剂可用于治疗或缓解与SK/IK/BK通道相关的疾病和症状。
  • Use of intermediate -conductance potassium channels and modulators for diagnosing and treating diseases having disturbed keratinocyte activity
    申请人:——
    公开号:US20040248099A1
    公开(公告)日:2004-12-09
    The invention relates to the use of intermediate-conductance, calcium-activated potassium channels and/or the nucleic acids coding for the same, from humans or mice, for the diagnosis, prevention and/or treatment of illnesses associated with disturbed keratinocyte activity. The invention also relates to the use of the same for identifying pharmacologically active substances. The invention further relates to the use of modulators of intermediate-conductance, calcium-activated potassium channels for the diagnosis, prevention and/or treatment of illnesses associated with disturbed keratinocyte activity.
    本发明涉及使用来自人类或小鼠的中间导电、钙激活钾通道和/或编码其的核酸,用于诊断、预防和/或治疗与干扰角质形成细胞活动相关的疾病。本发明还涉及使用相同的物质来鉴定药理活性物质。本发明进一步涉及使用中间导电、钙激活钾通道的调节剂,用于诊断、预防和/或治疗与干扰角质形成细胞活动相关的疾病。
  • Benzoxazoles: Potent Skeletal Muscle Relaxants
    作者:Joseph Sam、James N. Plampin
    DOI:10.1002/jps.2600530518
    日期:1964.5
  • NEW BENZIMIDAZOLONE-, BENZOXAZOLONE-, OR BENZOTHIAZOLONE DERIVATIVES AS ION CHANNEL MODULATING AGENTS
    申请人:NEUROSEARCH A/S
    公开号:EP1144387A1
    公开(公告)日:2001-10-17
查看更多

同类化合物

(N-{4-[(6-溴-2-氧代-1,3-苯并恶唑-3(2H)-基)磺酰基]苯基}乙酰胺) 钙离子载体A23187半镁盐 荧光增白剂EBF 苯并恶唑胺 苯并恶唑的取代物 苯并恶唑甲磺酰氯 苯并恶唑基-2-甲酰基-S-乙基-异缩氨基硫脲 苯并恶唑-2-羧酸酰肼 苯并恶唑-2-磺酸 苯并恶唑-2-甲酸 苯并恶唑-2-甲磺酸钠 苯并恶唑-2-乙酸 苯并恶唑 苯并噁唑-5-甲酸 苯并噁唑-2-羧酸乙酯 苯并噁唑-2-甲醛 苯并噁唑,4,7-二氯-2-(氯甲基)- 苯并噁唑,2-叠氮- 苯并噁唑,2-(氯甲基)-4,7-二氟- 苯并[d]恶唑-7-甲酸甲酯 苯并[d]恶唑-5-硼酸频哪醇酯 苯并[d]噁唑-6-甲醛 苯并[d]噁唑-2-羧酸甲酯 苯并[d]噁唑-2-甲醇 苯并[D]恶唑-7-胺 苯并[D]噁唑-4-基氨基甲酸叔丁酯 苯并[D]噁唑-2-羧酸钾 苯并-13C6-噁唑 离子载体 碘化二氢2-[3-(5,6-二氯-1,3-二乙基-1,3--2H-苯并咪唑-2-亚基)丙-1-烯基]-3-乙基-5-苯基苯并噁唑正离子 硫代偏糖醛 甲酰胺,N-乙基-N-[6-[(3-甲酰基苯氧基)甲基]-2-苯并噁唑基]- 甲酰胺,N-[6-(溴甲基)-2-苯并噁唑基]-N-乙基- 甲基硫酸1-甲基-8-[(甲基氨基甲酰)氧代]喹啉正离子 甲基6-氨基-1,3-苯并恶唑-2-羧酸酯 甲基2-氨基-1,3-苯并恶唑-5-羧酸酯 甲基1,3-苯并恶唑-2-基乙酸酯 甲基-2-乙基-1,3-苯并唑-5-羧酸乙酯 甲基-1,3-苯并唑-5-羧酸乙酯 环戊二烯并[e][1,3]恶嗪-5,6-二胺 环戊二烯并[d][1,3]恶嗪-6,7-二胺 溴氯唑酮 溴化二氢2-[3-[1-[4-[(乙酰氨基)磺基基]丁基]-5,6-二氯-3-乙基-1,3--2H-苯并咪唑-2-亚基]丙-1-烯基]-3-乙基-5-苯基苯并噁唑正离子 氰基二硫代亚氨酸(6-氯-2-氧代-3(2H)-苯并恶唑基)甲基甲基酯 氰基-二硫代亚氨酸甲基(2-氧代-3(2H)-苯并恶唑基)甲基酯 氯唑沙宗-2-13C-3-15N-羟基-18O 氯唑沙宗 氯化3-乙基-2-[2-(1-乙基-2,5-二甲基-1H-吡咯-3-基)乙烯基]苯并恶唑翁盐 昂唑司特 拂来星-d2