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3,5-diisopropylidene-1,2,4-trithiolane | 75100-49-1

中文名称
——
中文别名
——
英文名称
3,5-diisopropylidene-1,2,4-trithiolane
英文别名
3,5-Diisopropyliden-1,2,4-trithiolan;Bis(isopropyliden)-1,2,4-trithiolan;bis isopropylidene trithiane;diisopropylidene-[1,2,4]trithiolane;3,5-Di(propan-2-ylidene)-1,2,4-trithiolane
3,5-diisopropylidene-1,2,4-trithiolane化学式
CAS
75100-49-1
化学式
C8H12S3
mdl
——
分子量
204.381
InChiKey
VBTSMQDPZOMLRC-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

  • 沸点:
    296.4±33.0 °C(Predicted)
  • 密度:
    1.195±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    75.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • Dithio and Thiono Esters, 62. Reactions of Alkanedithioic Acid Dianions with Iodine, Sulfur, and Tin Compounds
    作者:Klaus Hartke、Uwe Wagner
    DOI:10.1002/cber.19961290612
    日期:1996.6
    The monoanion of the alkanedithioic acid 1a is oxidized with hypervalent iodine compounds to form the 1,2-dithiine 6, the monoanion of 1b yields the 1,2,4-trithiolane 7 and the dianions 2b, c furnish the 1,2,4,5-tetrathianes 3b, c. With diphenyltin or dimethyltin dichlorides 8 the monoanions of 1b, c afford the monothioacyl or bisthioacyl organotin sulfides 10a–c or 11a, b respectively. When treated
    所述alkanedithioic酸的单价阴离子1A与高价碘化合物氧化以形成1,2- dithiine 6,的单价阴离子1b中产生的1,2,4- trithiolane 7和二价阴离子2b中,C提供1,2,4- ,5-四硫杂环丁烷3b,c。与二苯基锡或二甲基二氯化锡8的1b,c的单阴离子分别生成单硫酰基或双硫酰基有机锡硫化物10a-c或11a,b。当用六甲基二硅氮烷锂处理时,10b发生分子内环化成1,3,2-二硫代锡烷9b; 10a被三乙胺去质子化为1,3,5-trithia-2-stanninane 13。二价阴离子2c与二氯化二苯基锡8反应,生成1,3,2-二硫杂锡碳烷9d,与二氯化二甲基锡形成1,2,4-三硫杂环戊烷16。图9d是由亚硫酰氯,二氯化硫,和二氯化二硫裂解以得到1,2,4,5- tetrathiane的复杂混合物3C和环状多硫化物1,2,3,4,5,6- hexathiepane
  • Bonnans-Plaisance, Chantal; Gressier, Jean-Claude; Levesque, Guy, Bulletin de la Societe Chimique de France, 1985, # 5, p. 891 - 899
    作者:Bonnans-Plaisance, Chantal、Gressier, Jean-Claude、Levesque, Guy、Mahjoub, Ahmed
    DOI:——
    日期:——
  • Dimeres et oligomers des dithioacides aliphatiques obtenus par action de peroxydes ou du rayonnement U. V.
    作者:Chantal Bonnans-Plaisance、Ahmed Mahjoub、Guy Levesque
    DOI:10.1016/s0040-4039(00)93651-7
    日期:1980.1
  • BONNANS-PLAISANCE C.; MAHJOUB A.; LEVESQUE G., TETRAHEDRON LETT., 1980, 21, NO 20, 1941-1942
    作者:BONNANS-PLAISANCE C.、 MAHJOUB A.、 LEVESQUE G.
    DOI:——
    日期:——
  • BONNANS-PLAISANCE, CH.;GRESSIER, J. -C.;LEVESOUE, GUY;MAHJOUB, AHMED, BULL. SOC. CHIM. FR., 1985, N 5, 891-899
    作者:BONNANS-PLAISANCE, CH.、GRESSIER, J. -C.、LEVESOUE, GUY、MAHJOUB, AHMED
    DOI:——
    日期:——
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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