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(S)-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate | 463298-63-7

中文名称
——
中文别名
——
英文名称
(S)-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate
英文别名
S-pentafluorophenyl 3-phenylpropanethioate;S-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate
(S)-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate化学式
CAS
463298-63-7
化学式
C15H9F5OS
mdl
——
分子量
332.294
InChiKey
CVHCJSQSGBQMJZ-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

  • 熔点:
    68.7-68.8 °C
  • 沸点:
    348.6±42.0 °C(Predicted)
  • 密度:
    1.42±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    7

SDS

SDS:b428f3ded785ae599d329fb852439d15
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反应信息

  • 作为反应物:
    描述:
    (S)-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate氢氧化钾 作用下, 以 丙酮 为溶剂, 反应 1.0h, 以100%的产率得到3-苯基丙酸
    参考文献:
    名称:
    通过在水中使用分子间自由基反应,可从醛高效合成硫酯和酰胺。
    摘要:
    发现了水溶性自由基引发剂2,2'-偶氮双[2-(2-咪唑啉-2-基)丙烷]二盐酸盐(VA-044)和表面活性剂十六烷基三甲基溴化铵(CTAB)的组合是在水中有效和直接合成有用的活性硫代酯(五氟苯基硫代酯)的最合适条件。另外,通过将胺加到水中的硫酯化反应混合物中来实现醛的直接酰胺化。
    DOI:
    10.1002/chem.200400754
  • 作为产物:
    描述:
    苯丙醛1,2,3,4,5-五氟-6-[(2,3,4,5,6-五氟苯基)二硫烷基]苯十六烷基三甲基溴化铵 、 2,2’-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride 作用下, 以 为溶剂, 反应 18.0h, 以73%的产率得到(S)-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate
    参考文献:
    名称:
    使用醛与二氟苯基二硫化物的分子间自由基反应在水中直接合成硫酯。
    摘要:
    发现水溶性自由基引发剂2,2'-偶氮双[2-(2-咪唑啉-2-基)丙烷]二盐酸盐(VA-044)和表面活性剂溴化十六烷基三甲基铵(CTAB)的混合物在水中有效直接合成有用的活性硫代酯(五氟苯基硫代酯)的最合适条件。
    DOI:
    10.1039/b202129c
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文献信息

  • Activation of hydrocinnamic acids with pentafluorophenol versus pentafluorothiophenol: Reactivity towards hexylamine
    作者:Fernanda M.F. Roleira、Fernanda Borges、Lourdes C.R. Andrade、José A. Paixão、Maria J.M. Almeida、Rui A. Carvalho、Elisiário J. Tavares da Silva
    DOI:10.1016/j.jfluchem.2008.09.013
    日期:2009.2
    In this work we describe and compare the synthesis of four new hexylamides of hydrocinnamic acids, namely hexylamide of hydrocinnamic, 3,4-dimethoxyhydrocinnamic, 4-hydroxy-3-methoxyhydrocinnamic and 3,4-dihydroxyhydrocinnamic acids via pentafluorophenyl esters (PFPEs) versus pentafluorophenyl thioesters (PFPTs) intermediates. It was found that the PRE are the best intermediates for this kind of synthesis giving reactions with less by products, easier work-up, higher overall yields and with the best reactivity towards hexylamine. The X-ray structures of two PRE are also reported. (C) 2008 Elsevier B.V. All rights reserved.
  • Efficient Synthesis of Thioesters and Amides from Aldehydes by Using an Intermolecular Radical Reaction in Water
    作者:Hisanori Nambu、Kayoko Hata、Masato Matsugi、Yasuyuki Kita
    DOI:10.1002/chem.200400754
    日期:2005.1.7
    (VA-044) and the surfactant, cetyltrimethyl-ammonium bromide (CTAB), was found to be the most suitable condition for the effective and direct synthesis of useful active thioesters (pentafluorophenyl thioesters) in water. In addition, the direct amidation of aldehydes was achieved by the addition of the amines to the thioesterification reaction mixture in water.
    发现了水溶性自由基引发剂2,2'-偶氮双[2-(2-咪唑啉-2-基)丙烷]二盐酸盐(VA-044)和表面活性剂十六烷基三甲基溴化铵(CTAB)的组合是在水中有效和直接合成有用的活性硫代酯(五氟苯基硫代酯)的最合适条件。另外,通过将胺加到水中的硫酯化反应混合物中来实现醛的直接酰胺化。
  • The direct synthesis of thioesters using an intermolecular radical reaction of aldehydes with dipentafluorophenyl disulfide in water
    作者:Hisanori Nambu、Kayoko Hata、Masato Matsugi、Yasuyuki Kita
    DOI:10.1039/b202129c
    日期:2002.5.9
    The combination of the water-soluble radical initiator, 2,2'-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (VA-044), and surfactant, cetyltrimethylammonium bromide (CTAB), was found to be the most suitable condition for the effective direct synthesis of useful active thioesters (pentafluorophenyl thioesters) in water.
    发现水溶性自由基引发剂2,2'-偶氮双[2-(2-咪唑啉-2-基)丙烷]二盐酸盐(VA-044)和表面活性剂溴化十六烷基三甲基铵(CTAB)的混合物在水中有效直接合成有用的活性硫代酯(五氟苯基硫代酯)的最合适条件。
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同类化合物

硫基丙酸苯酯 硫代乙酸S-[4-[二(2-氯乙基)氨基]苯基]酯 硫代乙酸 S-(2-乙基苯基)酯 乙硫酸,[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]-,S-苯基酯 S1,S2-二(4-氯苯基)乙烷二(硫代ate) S-苯基硫代异丁酸酯 S-苯基3-羟基硫代丁酸酯 S-苯基2-氟硫代乙酸酯 S-硫代乙酸苯酯 S-氯乙酰基-P-巯基甲苯 S-丙酰基-p-疏基甲苯 S-[4-[2-[4-(2-苯乙炔基)苯基]乙炔基]苯基]硫代乙酸酯 S-(三氟乙酰基)-4-疏基甲苯 S-(4-甲基苯基)硫代乙酸酯 S,S′-[1,4-亚苯基二(2,1-乙炔二基-4,1-亚苯基)]双(硫代乙酸酯) O-乙基S-(4-甲基苯基)单硫代草酸酯 4-溴苯基硫代乙酸酯 4-(S-乙酰基硫代)苯甲醛 4,4-二甲基-1-氧代-1-(苯基硫基)-2-戊烷基乙酸酯 3-氧代-3-(4-甲氧基苯氧基)丙酸 2-甲基苯硫酚乙酸酯 1-乙酰巯基-4-碘苯 S-(2-methoxyphenyl) 4-cyclopropylidenebutanethioate phenyl 3-methyl-2-cyclohexene-1-carbothioate S-(2-fluorophenyl) 2-methylpropanethioate 2-isopropylidenedithiosuccinic acid di-S-(4-fluorophenyl) ester thioacetic acid S-(4-ethyl-phenyl ester) S-phenyl 2,3-dimethyl-2-butenethioate 3-phenylsulfanylcarbonyl-propionic acid ethyl ester S-phenyl (3r,5r,7r)-adamantane-1-carbothioate (E)-S-Phenyl 4,4-dimethylpent-2-enethioate S-phenyl 2-(2-methoxyphenyl)ethanethioate S-phenyl (2R,3R)-3-(tert-butyldimethylsiloxy)-2-methyl-3-phenylpropanethioate S-(4-fluorophenyl) thiopivalate S-phenyl 2-methylbutanethioate S-phenyl 3-(phenyl((trimethylsilyl)oxy)amino)-3-(thiophen-2-yl)propanethioate S-phenyl 3-(4-bromophenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-phenyl-3-(phenyl((triethylsilyl)oxy)amino)propanethioate S-phenyl 3-cyclohexyl-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-(((tert-butyldimethylsilyl)oxy)(phenyl)amino)-3-phenylpropanethioate S-phenyl 3-(4-methoxyphenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-(phenyl((trimethylsilyl)oxy)amino)-3-(p-tolyl)propanethioate S-phenyl 3-(4-fluorophenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-phenyl-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate (E)-S-phenyl 5-phenyl-3-(phenyl((trimethylsilyl)oxy)amino)pent-4-enethioate S-phenyl 3-hydroxy-3-(4-methoxyphenyl)propanethioate S-phenyl 2-methyl-3-oxobutanethioate S-phenyl O-acetyl(thioglycolate) 6-Nitro-9-oxodecansaeure-phenylthioester 2-isopropylidenedithiosuccinic acid di-S-p-tolyl ester