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5-trifluoromethyl-3-(2-furyl)-5-hydroxy-4,5-dihydro-1H-pyrazolyl-1-carbohydrazide | 1174009-11-0

中文名称
——
中文别名
——
英文名称
5-trifluoromethyl-3-(2-furyl)-5-hydroxy-4,5-dihydro-1H-pyrazolyl-1-carbohydrazide
英文别名
3-(furan-2-yl)-5-hydroxy-5-(trifluoromethyl)-4H-pyrazole-1-carbohydrazide
5-trifluoromethyl-3-(2-furyl)-5-hydroxy-4,5-dihydro-1H-pyrazolyl-1-carbohydrazide化学式
CAS
1174009-11-0
化学式
C9H9F3N4O3
mdl
——
分子量
278.191
InChiKey
APHLMNMEJGNMDA-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):
    0.6
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    104
  • 氢给体数:
    3
  • 氢受体数:
    8

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:
    胡椒醛5-trifluoromethyl-3-(2-furyl)-5-hydroxy-4,5-dihydro-1H-pyrazolyl-1-carbohydrazide乙醇 为溶剂, 反应 7.0h, 以65%的产率得到(E)-N'-(1,3-dioxobenzyliden-5-yl)-[5-trifluoromethyl-3-(2-furyl)-5-hydroxy-4,5-dihydro-1H-pyrazol-1-yl]carbohydrazide
    参考文献:
    名称:
    New trifluoromethyl-containing (E)-N′-arylidene-[3-alkyl(aryl/heteroaryl)-4,5-dihydro-1H-pyrazol-1-yl]carbohydrazides: Synthesis, crystal structure and antimicrobial/antioxidant activity
    摘要:
    A new series of twenty-one trifluoromethyl-containing (E)-N'-arylidene-1H-pyrazole-1-carbohydrazides (4) was synthesized by the cyclocondensation reactions of six 3-alkyl(aryl/heteroaryl)-5-trifluoromethyl-5-hydroxy-4,5-dihydro-1H-pyrazole-1-carbohydrazides (2) with eleven aryl/heteroaryl aldehydes and acetophenone (3) in 52-97% yields and six new carbohydrazides 2 were easily obtained from the reaction of 1,1,1-trifluoro-4-alkyl(aryl/heteroaryl)-4-methoxy-3-alken-2-ones (1) with carbohydrazide. Subsequently, four examples of carbohydrazides 4 were fully studied by X-ray diffraction and the twenty-seven pyrazolyl-carbohydrazides 2 and 4 screened for their antioxidant and antimicrobial proprieties and evaluated by DPPH and MIC methods, respectively. Both series 2 and 4 showed ability to capture DPPH free radical for IC50 from 47.57 to 487 mu g/mL. Most of the compounds presented fungistatic and bacteriostatic activity only for high MIC levels ranging from 0.25 mg/mL to 0.5 mg/mL. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2011.12.010
  • 作为产物:
    描述:
    甲酰肼 、 (E)-1,1,1-Trifluoro-4-furan-2-yl-4-methoxy-but-3-en-2-one 以 乙醇 为溶剂, 以85%的产率得到5-trifluoromethyl-3-(2-furyl)-5-hydroxy-4,5-dihydro-1H-pyrazolyl-1-carbohydrazide
    参考文献:
    名称:
    New trifluoromethyl-containing (E)-N′-arylidene-[3-alkyl(aryl/heteroaryl)-4,5-dihydro-1H-pyrazol-1-yl]carbohydrazides: Synthesis, crystal structure and antimicrobial/antioxidant activity
    摘要:
    A new series of twenty-one trifluoromethyl-containing (E)-N'-arylidene-1H-pyrazole-1-carbohydrazides (4) was synthesized by the cyclocondensation reactions of six 3-alkyl(aryl/heteroaryl)-5-trifluoromethyl-5-hydroxy-4,5-dihydro-1H-pyrazole-1-carbohydrazides (2) with eleven aryl/heteroaryl aldehydes and acetophenone (3) in 52-97% yields and six new carbohydrazides 2 were easily obtained from the reaction of 1,1,1-trifluoro-4-alkyl(aryl/heteroaryl)-4-methoxy-3-alken-2-ones (1) with carbohydrazide. Subsequently, four examples of carbohydrazides 4 were fully studied by X-ray diffraction and the twenty-seven pyrazolyl-carbohydrazides 2 and 4 screened for their antioxidant and antimicrobial proprieties and evaluated by DPPH and MIC methods, respectively. Both series 2 and 4 showed ability to capture DPPH free radical for IC50 from 47.57 to 487 mu g/mL. Most of the compounds presented fungistatic and bacteriostatic activity only for high MIC levels ranging from 0.25 mg/mL to 0.5 mg/mL. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2011.12.010
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同类化合物

辛基羟乙基咪唑啉 辛基羟乙基咪唑啉 苯丙酸,3,4-二羟基-a-羰基- 肉豆蔻基羟乙基咪唑啉 硬脂酸,氨基乙基乙醇胺酰胺-咪唑啉,羧甲基化钠盐 甲基-(1-甲基-吡咯烷-2-亚基)-胺 甲基(5-甲基-1,2-恶唑-3-基)氨基甲酸酯 油基胺乙基咪唑啉 油基羟乙基咪唑啉 氯代醋酸钠与4,5-二氢-十一烷基-1H-咪唑-1-乙醇和氢氧化钠的反应产物 氯二甲基(1-甲基-1-丙烯基)硅烷 氯-乙酸反应产物与2-庚基-4,5-二氢-1H-咪唑-1-乙醇和氢氧化钠 月桂基羟乙基咪唑啉 恶唑-4-基氨基甲酸叔丁酯 异硬脂基羟乙基咪唑啉 异噁隆 异丙基亚氨基吡咯烷 噻唑-2,4-二胺 噁唑-4-胺 叔-丁基2-氨基-6,7-二氢吡唑并[1,5-A]吡嗪-5(4H)-甲酸基酯 十七碳-2-烯基-4,5-二氢-1H-咪唑-1-乙醇盐酸盐 偶氮引发剂VA-064 依凡达明 二氨基吡唑 乙基3-(乙基氨基)-5-甲基-1,2-恶唑-4-羧酸酯 alpha-(氯甲基)-2-异丙基-5-硝基-2H-咪唑-2-乙醇 alpha,4,4-三甲基-2-十一烷基-2-咪唑啉-1-乙醇 Z-2-(8-十七烯基)-4,5-二氢-1H-咪唑-1-乙醇 N-甲基异噻唑-3-胺盐酸 N-甲基-N-(5-甲基-3-异恶唑基)-乙酰胺 N-甲基-3-氨基吡唑 N-甲基-2-吡咯烷酮肟 N-甲基-1,2-噻唑-3-胺1,1-二氧化物 N-环己基-1,2-噻唑-3-胺1,1-二氧化物 N-叔-丁基-5-甲基-2H-吡唑-3-胺 N-乙基-N-(5-甲基-3-异恶唑基)-乙酰胺 N-乙基-1,2-噻唑-3-胺1,1-二氧化物 N-乙基-1,2,5-恶二唑-3,4-二胺 N-{(E)-[(4-氨基-1,2,5-恶二唑-3-基)氨基]亚甲基}乙酰胺 N-[2-[2-[(E)-十七碳-8-烯基]-4,5-二氢咪唑-1-基]乙基]乙烷-1,2-二胺 N-[2-[2-(13-二十一碳烯-1-基)-4,5-二氢-1H-咪唑-1-基]乙基]乙二胺 N-[2-(4,5-二氢-2-十九烷基-1H-咪唑-1-基)乙基]乙二胺 N-[2-(4,5-二氢-2-十一烷基-1H-咪唑-1-基)乙基]乙二胺 N-[(2Z)-哌嗪-2-亚基]-2,2,2-三氟乙酰肼 N-[(2-甲基苯基)氨基甲硫杂酰]-2-(4-羰基-2-苯基喹唑啉-3(4H)-基)-3-苯基丙酰胺 N-BOC-4-氨基噻唑 N-3-异恶唑氨基甲酸叔丁酯 N-(噻二唑-4-基)氨基甲酸乙酯 N-(5-叔丁基-1H-吡唑-3-基)氨基甲酸甲酯 N-(4,5-二甲基-3-异噁唑)氨基甲酸1,1-二甲基乙酯