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4,5,6,7-四氢苯并[1,2]二硫-3-硫酮 | 14085-34-8

中文名称
4,5,6,7-四氢苯并[1,2]二硫-3-硫酮
中文别名
——
英文名称
4,5,6,7-tetrahydro-3H-1,2-benzodithiole-3-thione
英文别名
4,5,6,7-tetrahydro-3H-benzo[c][1,2]dithiole-3-thione;4,5,6,7-Tetrahydro-3H-1,2-benzodithiol-3-thion;4,5,6,7-tetrahydrobenzo[1,2]dithiole-3-thione;CJ11792;4,5,6,7-tetrahydro-benzo[1,2]dithiole-3-thione;4,5,6,7-tetrahydro-benzo[1,2]dithiol-3-thione;4,5,6,7-tetrahydro-1,2-benzodithiole-3-thione
4,5,6,7-四氢苯并[1,2]二硫-3-硫酮化学式
CAS
14085-34-8
化学式
C7H8S3
mdl
——
分子量
188.339
InChiKey
WNPWNYMVKHOGRA-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:
    92 °C
  • 沸点:
    283.37°C (rough estimate)
  • 密度:
    1.3118 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    82.7
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2930909090

SDS

SDS:8d4ca037f01a7c272e164b6179fcd393
查看

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

点击查看最新优质反应信息

文献信息

  • Thionation with the Reagent Combination of Phosphorus Pentasulfide and Hexamethyldisiloxane
    作者:Thomas J. Curphey
    DOI:10.1021/jo0256742
    日期:2002.9.1
    The combination of P4S10 and hexamethyldisiloxane efficiently converts esters, lactones, amides, lactams, and ketones to their corresponding thiono derivatives. In the presence of elemental sulfur, 3-oxoesters are converted to dithiolethiones by this reagent. Yields are comparable to or superior to those obtained with Lawesson's reagent. The method has the advantage that reagent-derived byproducts
    P4S10和六甲基二硅氧烷的组合可将酯,内酯,酰胺,内酰胺和酮有效地转化为其相应的代衍生物。在元素的存在下,该试剂将3-氧代酯转化为二酮。产率与使用劳森试剂获得的产率相当或更高。该方法的优点在于,可以通过简单的解后处理或通过硅胶过滤而不是通过劳氏试剂所要求的色谱法来除去试剂衍生的副产物。
  • Abrogation of Hyperosmotic Impairment of Insulin Signaling by a Novel Class of 1,2-Dithiole-3-thiones through the Inhibition of S6K1 Activation
    作者:Eun Ju Bae、Yoon Mee Yang、Sang Geon Kim
    DOI:10.1124/mol.107.044347
    日期:2008.5
    factor-alpha-induced hepatic insulin resistance via AMP-activated protein kinase-dependent p70S6 kinase (S6K) 1 inhibitory pathway. This study investigated whether oltipraz and a novel class of 1,2-dithiole-3-thiones were capable of preventing insulin resistance induced by hyperosmotic stress, thereby enhancing insulin-dependent signals, and, if so, whether the restoration of insulin signal was mediated
    来自该实验室的先前研究表明,酮和合成的二酮通过AMP激活的蛋白激酶依赖性p70S6激酶(S6K)1抑制途径预防​​肿瘤坏死因子-α诱导的肝胰岛素抵抗。这项研究调查了oltipraz和一类新型的1,2-二代3-酮是否能够预防高渗应激诱导的胰岛素抵抗,从而增强胰岛素依赖性信号,如果可以,是否介导了胰岛素信号的恢复抑制高渗应激刺激的S6K1活性。在HepG2细胞中,oltipraz处理抑制了胰岛素受体底物(IRS)1丝氨酸磷酸化,这是山梨糖醇甘露醇氯化钠诱导的高渗应激诱导的胰岛素抵抗的标志。所以,这可以使细胞恢复胰岛素信号,这可以通过IRS1的丝氨酸酪氨酸磷酸化比率的降低以及Akt和糖原合酶激酶(GSK)3beta磷酸化的增加来证明。高渗胁迫明显激活了S6K1;oltipraz预处理完全消除了S6K1激活。使用显性阴性S6K1的实验支持S6K1在高渗透压刺激的IRS1磷酸
  • The behavior of some Wittig reagents toward 4,5,6,7-tetrahydro-3<i>H</i>-1,2-benzo[1,2]dithiole-3-thione
    作者:Ewies F. Ewies、Naglaa F. El-Sayed、Leila S. Boulos
    DOI:10.1080/17415993.2019.1606224
    日期:2019.9.3
    ABSTRACT Novel synthetic route for phosphanylidene-benzothiophenethione, benzothiaphosphinine-4-thione, triphenylphosphoranylidenecyclobutane and benzodithiolylidenephosphonate derivatives has been proposed through reactions of 4,5,6,7-tetrahydro-3H-1,2-benzodithiole-3-thione with different Wittig and Wittig–Horner reagents. All new synthesized compounds were fully characterized with elemental and
    摘要 通过 4,5,6,7-四氢-3H-1,2-苯并二醚-3-酮与不同 Wit 的反应,提出了亚膦基-苯并噻吩酮、苯并噻吩-4-酮、三苯基正膦亚基环丁烷和苯并二亚磷酸酯衍生物的合成路线。 Wittig-Horner 试剂。所有新合成的化合物都通过元素和光谱分析进行了充分表征。图形概要
  • Synthesis of new dithiolethione derivatives: 5-(1-hydroxyiminoalkyl)-1,2-dithiole-3-thiones and 5-acyl-1,2-dithiole-3-thiones
    作者:M. Abazid、H. O. Bertrand、M. O. Christen、J. L. Burgot
    DOI:10.1039/c39940000131
    日期:——
    A synthetic pathway to obtain, in three steps, acceptable yields of 5-acyl-1,2-dithiole-3-thiones is described.
    本文介绍了一种合成途径,通过三个步骤就能获得收率可接受的 5-酰基-1,2-二代-3-酮。
  • Heterocyclic thione compounds and their use as biocides
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0249328A2
    公开(公告)日:1987-12-16
    Compounds having a 5 membered, nitrogen containing ring with a thione group adjacent to a nitrogen atom substituted with an OR group have antimicrobial properties. Metal complexes or salts of these compounds also have antimicrobial properties. The compounds, or the metal complexes or salts thereof, can be used as a cutting fluid preservative, a wood preservative, in cooling water applications or as an antimicrobial agent in a paint. Some of the compounds are new. The metal complexes or salts are new.
    具有 5 个成员的含氮环,其中一个酮基团与一个被 OR 基团取代的氮原子相邻的化合物具有抗菌特性。这些化合物的属络合物或盐也具有抗菌特性。这些化合物或其属络合物或盐可用作切削液防腐剂、木材防腐剂、冷却应用或涂料中的抗菌剂。其中一些化合物是新型的。属络合物或盐是新的。
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同类化合物

四硫杂富瓦烯-D4 四硫富瓦烯 四(戊硫代)四硫富瓦烯 四(十八烷基硫代)四硫富瓦烯 四(乙硫基)四硫富瓦烯[有机电子材料] 双(亚乙基二硫醇)四硫代富瓦烯 双(三亚甲基二硫代)四硫富瓦烯 三(四硫富瓦烯)双(四氟硼酸盐)复合物 [1,3]二噻唑并[4,5-d]-1,3-二噻唑,2,5-二(1,3-二硫醇-2-亚基)- 5-甲基二硫杂环戊烯-3-硫酮 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-羧酸乙酯 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-甲腈 5,6-二氢-4H-环戊并[1,2]二硫代-3-硫酮 4,4’,5-三甲基四硫富瓦烯 4-甲基二硫杂环戊烯-3-硫酮 4-新戊基-3H-1,2-二硫杂环戊烯-3-硫酮 4,5-二甲基-3H-1,2-二硫醇-3-酮 4,5,6,7-四氢苯并[1,2]二硫-3-硫酮 4,4’-二甲基连四硫富瓦烯 4,4,5,5,6,6,7,7-八氢二苯并四硫富瓦烯 3H-1,2-二硫杂环戊二烯-3-酮 3H-1,2-二硫杂环戊二烯-3-硫酮 2-(4,5-二甲基-1,3-二硫杂环戊烯-2-亚基)-4,5-二甲基-1,3-二硫杂环戊烯 2,3,6,7-四(2-氰乙基硫代)四硫富瓦烯 1,3-二噻唑,2-[4,5-二(癸基硫代)-1,3-二硫醇-2-亚基]-4,5-二(癸基硫代)- 1,3-二噻唑,2-[4,5-二(十四烷基硫代)-1,3-二硫醇-2-亚基]-4,5-二(十四烷基硫代)- 1,3-二噻唑,2-[4,5-二(十一烷基硫代)-1,3-二硫醇-2-亚基]-4,5-二(十一烷基硫代)- (四甲基硫)四硫富瓦烯 3-[[2-[4,5-Bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-[3-[[2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-[3-[[2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-[3-[[2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-(2-cyanoethylsulfanyl)-1,3-dithiol-4-yl]sulfanyl]propylsulfanyl]-1,3-dithiol-4-yl]sulfanyl]propylsulfanyl]-1,3-dithiol-4-yl]sulfanyl]propylsulfanyl]-1,3-dithiol-4-yl]sulfanyl]propanenitrile 4,5-Bis-{2-[2-(2-iodo-ethoxy)-ethoxy]-ethylsulfanyl}-4',5'-bis-methylsulfanyl-[2,2']bi[[1,3]dithiolylidene] 2-<4,5-bis(methylthio)-1,3-dithiol-2-ylidene>-5-(thiopyran-4-ylidene)-1,3,4,6-tetrathiapentalene 2,3-bis(2-cyanoethylthio)-6,7-bis(2-hydroxyethylthio)tetrathiafulvalene 4,5-bis(decylthio)-4'-(3-cyanopropyl)thio-5-methyltetrathiafulvalene 4,5,4',5'-Tetrakis-trimethylsilanylethynyl-[2,2']bi[[1,3]dithiolylidene] bis(Dimethylvinylenedithio)tetrathiafulvalene 2,3-Bis{2-[2-(2-chloroethoxy)ethoxy]ethylthio}-6-(2-cyanoethylthio)-7-methylthiotetrathiafulvalene 3-[5-(2-Cyano-ethylselanyl)-2-methylsulfanyl-[1,3]dithiol-4-ylselanyl]-propionitrile 2-(4-Pent-4-ynyl-[1,3]dithiol-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine 2-(4-Nonadeca-4,6-diynyl-[1,3]dithiol-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine 5-Trifluoromethyl-[1,2]dithiole-3-thione 4-[(trimethylsilyl)ethynyl]-5-methyl-4',5'-ethylenedithiotetrathiafulvalene [4-Methyl-5-methylsulfanyl-[1,2]dithiol-(3Z)-ylidene]-thioacetic acid S-methyl ester 1,3-Dithiolo[4,5-b][1,4]dithiin,5,6-dihydro-2-[4-(9-decynyl)-1,3-dithiol-2-ylidene]- di(vinylthio)ethylenedithiotetrathiafulvalene 2,3:8,9-Bis(ethylendithio)-1,4,7,10-tetrathiafulvalen, CT-Komplex mit 2,5-Bis(cyanimino)-2,5-dihydro-3,6-diiodthieno<3,2-b>thiophen 4-ethyl-2-isopropylidene-[1,3]dithiole 2-[1-Chloro-1-methylsulfanylcarbonyl-meth-(Z)-ylidene]-5-methylsulfanyl-[1,3]dithiole-4-carbothioic acid S-methyl ester tetra(vinylthio)tetrathiafulvalene