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cis-3,5-Dimethyl-1,2,4-trithiolan | 38348-23-1

中文名称
——
中文别名
——
英文名称
cis-3,5-Dimethyl-1,2,4-trithiolan
英文别名
cis-3,5-dimethyl-1,2,4-trithiolane;3,5-dimethyl-1,2,4-trithiolane;Syn-3,5-dimethyl-1,2,4-trithiolane;(3S,5R)-3,5-dimethyl-1,2,4-trithiolane
cis-3,5-Dimethyl-1,2,4-trithiolan化学式
CAS
38348-23-1
化学式
C4H8S3
mdl
——
分子量
152.306
InChiKey
HFRUNLRFNNTTPQ-ZXZARUISSA-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):
    2.4
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    75.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    bis(1-chloroethyl) sulfide 在 sodiumsulfide nonahydrate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 10.0h, 生成 cis-3,5-Dimethyl-1,2,4-trithiolantrans-3,5-Dimethyl-1,2,4-trithiolan
    参考文献:
    名称:
    1,3,5-三硫烷和一氯化硫/硫化钠:3,5-二取代的1,2,4-三硫杂环戊烷的替代途径
    摘要:
    在温和条件下用 S2Cl2 和 Na2S 处理取代的 1,3,5-三硫杂环戊烷,得到 3,5-二取代的 1,2,4-三硫杂环戊烷,作为非对映异构体的混合物。图形概要
    DOI:
    10.1080/17415993.2020.1810251
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文献信息

  • Hug; Janeba-Bartoszewicz; Filipiak, Polish Journal of Chemistry, 2008, vol. 82, # 4, p. 883 - 892
    作者:Hug、Janeba-Bartoszewicz、Filipiak、Pedzinski、Kozubek、Marciniak
    DOI:——
    日期:——
  • 1,3,5-Trithianes and sulfur monochloride/sodium sulfide: an alternative route to 3,5-disubstituted 1,2,4-trithiolanes
    作者:Damiano Tanini、Francesca Trapani、Antonella Capperucci
    DOI:10.1080/17415993.2020.1810251
    日期:2020.11.1
    Treatment of substituted 1,3,5-trithianes with S2Cl2 and Na2S under mild conditions provides 3,5-disubstituted 1,2,4-trithiolanes, as mixture of diastereoisomers. GRAPHICAL ABSTRACT
    在温和条件下用 S2Cl2 和 Na2S 处理取代的 1,3,5-三硫杂环戊烷,得到 3,5-二取代的 1,2,4-三硫杂环戊烷,作为非对映异构体的混合物。图形概要
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同类化合物

3,5-二甲基-1,2,4-三硫环戊烷 3,5-二异丁基-1,2,4-三硫环戊烷 3,5-二乙基-1,2,4-三硫杂环戊烷 3,5-二(1-甲基乙基)-1,2,4-三硫杂戊环 3,3,5,5-四甲基-1,2,4-三硫杂戊环 1,2,4-三硫杂戊环 1,1,3,3,7,7,9,9-Octamethyl-5,10,11-trithiadispiro<3.1.3.2>undecan-2,8-dithion 4-methyl-1,2,3-trithiolane Tetrafluor-1,2,3-trithiolan N,N,N',N'-tetra-tert-butyl-1,2,4-trithiolane-3,3,5,5-tetracarboxamide 3-Methyl-1,2,4-trithiolane 3,5-Ditert-butyl-1,2,4-trithiolane spirocyclohexyl-1,2,4-trithiolane 4-S-oxide spirocyclohexyl-1,2,4-trithiolane 1-S-oxide cis-3,5-Dimethyl-1,2,4-trithiolan trans-3,5-Diethyl-1,2,4-trithiolane cis-3,5-Diethyl-1,2,4-trithiolan 2,2,8,8-tetrachloro-1,1,3,3,7,7,9,9-octamethyl-5,10,11-trithiadispiro[3.1.3.2]undecane 3,3,5,5-bis(pentamethylene)-1,2,4-trithiolane trans-3,5-Dimethyl-1,2,4-trithiolan (3S,5S)-3,5-Bis(2-methylpropyl)-1,2,4-trithiolane (3R,5S)-3,5-Bis(2-methylpropyl)-1,2,4-trithiolane 3,5-Dibutyl-1,2,4-trithiolane 1,8-Dimethyl-2,6,9,12,13-pentathia-dispiro[4.1.4.2]tridecane (3S,5R)-3-Ethyl-5-methyl-1,2,4-trithiolane trans-3-Ethyl-5-methyl-1,2,4-trithiolane 1,2,3-trithiolane 3,5-Dimethyl-3,5-diaethyl-1,2,4-trithiolan 4-<(trimethylsilyl)methyl>-1,2,3-trithiacyclopentane 3,3,5,5-tetramethyl-1,2,4-trithiolane 4-oxide 3,3,5,5-tetramethyl-1,2,4-trithiolane 1-oxide (1R,2R,6R,7R)-3,4,5-trithiatricyclo[5.2.1.02,6]dec-8-ene 1,2,4-Trithiolane, 3,5-dimethyl, #1 2-(1,2,3-trithiaspiro[4.4]nonan-9-yl)ethanethioic S-acid (3S)-3-methyl-1,2,4-trithiolane (3R)-3-propan-2-yl-1,2,4-trithiolane (3S)-3-propan-2-yl-1,2,4-trithiolane (3R,5R)-3,5-bis(2-methylpropyl)-1,2,4-trithiolane 1,2,4-Trithiolane, 5-ethenyl-3-ethyl (1R,2S,6R,7S)-3,4,5-trithiatricyclo[5.2.1.02,6]dec-8-ene Trithiolan-4-ylphosphonic acid (3R)-3-methyl-1,2,4-trithiolane (3R)-3-methyl-1,2,4-trithiolane;(3S)-3-methyl-1,2,4-trithiolane 1,2,4-Trithiolane, 3-ethyl-5-(1-methylethyl), #1 1,2,4-Trithiolane, 3-methyl-5-(1-methylethyl), #1 4,6a-Dihydro-3aH-cyclopenta[d][1,2,3]trithiole dispiro[adamantane-2,3'-(1,2,4)-trithiolane-5',2'-adamantane] 1,1,3,3,7,7,9,9-octamethyl-5,10,11-trithiadispiro<3.1.3.2>undecane-2,8-dione trans-2,2'-(1,2,4-Trithiolan-3,5-diyliden)bis(3,3-dimethylbutyronitril) 3,5-diisopropylidene-1,2,4-trithiolane