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phenyl thiopalmitate | 75839-74-6

中文名称
——
中文别名
——
英文名称
phenyl thiopalmitate
英文别名
thiopalmitic acid S-phenyl ester;Thiopalmitinsaeure-S-phenylester;S-phenyl hexadecanethioate
phenyl thiopalmitate化学式
CAS
75839-74-6
化学式
C22H36OS
mdl
——
分子量
348.593
InChiKey
MYXGUGJMNGVKDF-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:
    28-28.5 °C(Solv: acetone (67-64-1))
  • 沸点:
    448.6±14.0 °C(Predicted)
  • 密度:
    0.96±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    9.5
  • 重原子数:
    24
  • 可旋转键数:
    16
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.68
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    phenyl thiopalmitate 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 反应 6.0h, 以99%的产率得到1-十六烷醇
    参考文献:
    名称:
    Liu, Hsing-Jang; Bukownik, Rudolf R.; Pednekar, Purushottam R., Synthetic Communications, 1981, vol. 11, # 8, p. 599 - 604
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    Notes: Reactions of Long-Chain Acids with Thiolacetates
    摘要:
    DOI:
    10.1021/jo01090a616
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文献信息

  • Zinc Promoted Convenient and General Synthesis of Thiol Esters
    作者:H. M. Meshram、Gondi Sudershan Reddy、K. Hima Bindu、J. S. Yadav
    DOI:10.1055/s-1998-1797
    日期:1998.8
    Synthesis of thiol esters from acyl chlorides and thiols in the presence of activated zinc is described. The recovery of zinc and its reuse makes the procedure more economic.
    描述了在活化锌存在下由酰氯和硫醇合成硫羟酸酯。锌的回收和再利用使该过程更加经济。
  • Morgenstern; Kunz; Mayer, Pharmazie, 1969, vol. 24, # 8, p. 450 - 453
    作者:Morgenstern、Kunz、Mayer
    DOI:——
    日期:——
  • Microwave Thermolysis VII: Oxidative Coupling of Thiol Acetates and Esters Using “Clayan” in Dry Media
    作者:H. M. Meshram、A. Bandyopadhyay、G. S. Reddy、J. S. Yadav
    DOI:10.1080/00397919908086432
    日期:1999.8.1
    Disulfide bond formation by the oxidative cleavage of thiol acetates and thiol esters using "Clayan" under microwave irradiation is described. The non-metallic and inexpensive nature of the reagent are the important features of the procedure.
  • Liu, Hsing-Jang; Sabesan, Subramaniam Iyer, Canadian Journal of Chemistry, 1980, vol. 58, p. 2645 - 2648
    作者:Liu, Hsing-Jang、Sabesan, Subramaniam Iyer
    DOI:——
    日期:——
  • Synthesis of Some Thiol Esters of Long-Chain Fatty Acids
    作者:GEORGE S. SASIN、RICHARD SASIN、NICHOLAS CAPRON
    DOI:10.1021/jo01114a007
    日期:1956.8
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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