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1,2-Bis-(methylsulfinyl)-ethan | 10349-04-9

中文名称
——
中文别名
——
英文名称
1,2-Bis-(methylsulfinyl)-ethan
英文别名
2,5-Dithiahexan-2,5-dioxid;1,2-Bis(methylsulfinyl)ethane
1,2-Bis-(methylsulfinyl)-ethan化学式
CAS
10349-04-9
化学式
C4H10O2S2
mdl
——
分子量
154.254
InChiKey
JHKDMTXEOGSFBK-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:
    445.5±28.0 °C(Predicted)
  • 密度:
    1.358±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.6
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    72.6
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    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

  • Sulphur ligand metal complexes. Part 6. Copper complexes of 2,5-dithiahexane and 3,6-dithiaoctane
    作者:Eric W. Ainscough、Andrew M. Brodie、Kevin C. Palmer
    DOI:10.1039/dt9760002375
    日期:——
    dithioethers 2,4-dithiahexane (dth) and 3,6-dithiaoctane (dto) form the following complexes, some of which have been previously reported, with CuII and CuI: Cu(BF4)2L2 and CuX2L (L = dth or dto, X = Cl or Br); [CuL2]X (L = dth or dto. X = SF,: L = dth, X = ClO4); CuXL (L = dth, X = Cl, Br, or I; L = dto, X = I or SCN); and (CuCl)2L (L = dto, X = Cl or Br). The complexes have been characterized by a variety
    二硫醚2,4-二硫代己烷(dth)和3,6-二硫代辛烷(dto)与Cu II和Cu I形成以下配合物,其中一些已被报道:Cu(BF 4)2 L 2和CuX 2 L(L = dth或dto,X = Cl或Br);[CuL 2 ] X(L = dth或dto。X= SF,:L = dth,X = ClO 4);CuXL(L = dth,X = Cl,Br或I; L = dto,X = I或SCN);和(CuCl)2L(L = dto,X = Cl或Br)。复合物已通过多种物理化学技术进行了表征,并在可能的地方提出了结构。讨论了铜-硫键的性质,并得出结论,硫醚不会与Cu II形成明显的π键。螯合的硫醚配体容易被取代,例如从CuCl 2 L(L = dth或dto)和CuCl(dth)取代。通过各种配体(例如吡啶,吡咯烷,2,2'-联吡啶基,乙二胺,PPh 3,PMe 3 S和Na [S 2 PMe
  • The chemistry of quadrivalent lanthanoids. Part 2. Preparation and properties of cerium tetrachloride complexes and a comparison with their uranium analogues
    作者:John Barry、Jan G. H. du Preez、Thomas I. Gerber、Annelie Litthauer、Hans E. Rohwer、Bernardus J. van Brecht
    DOI:10.1039/dt9830001265
    日期:——
    Cerium tetrachloride complexes, viz. [CeCl4L2] and [CeCI4L] where L = a uni- or bi-dentate arsine oxide, a phosphine oxide, a sulphoxide, or an amide, have been prepared. The thermal degradation behaviour of the solids could be divided into three patterns, one of which consists of loss of a chlorine atom only. It was indicated that [CeCI4(ipae)2] could act as a substitute for the thermally unstable
    四氯化铈配合物,即。已经制备了[CeCl 4 L 2 ]和[CeCl 4 L],其中L =单齿或双齿氧化砷,氧化膦,亚砜或酰胺。固体的热降解行为可以分为三种模式,其中一种仅由氯原子的损失组成。指出[CeCl 4(ipae)2 ]可以代替热不稳定的CeCl 4进行溶液研究[ipae = 1-(二异丙基氨基)乙醛。[ CeCl 4(ipae)2 ]和Cs 2 [CeCI 6 ]溶液的分解速率研究]在不同的溶剂中表示分解反应相对于铈(IV)是一阶的,并且其反应速率大约与溶剂的供体数成正比。亚硫酰氯中的溶液可以无限期稳定。在配位行为,红外光谱,非水电导行为和溶剂镜性质方面,将研究的化合物与其铀(IV)类似物进行了比较。在加入CeCl 4和UCI 4个络合物证明几乎在所有方面非常类似,不同之处在于这些铈(IV)更solvoscopic。铈(IV)与铀(IV)之间的一些区别)可能最好用4 f和5 f金属字符之间的差异而不是尺寸差异来解释。
  • Disulfoxide complexes with lanthanum perchlorate
    作者:Arden P. Zipp、Sybil G. Zipp
    DOI:10.1016/0022-1902(80)80013-3
    日期:1980.1
    The synthesis and characterization of the complexes between La(ClO4)3 and eleven disulfoxides with the formula RS(O) (CH2)xS(O)R are reported. In all cases, the lathanum ions is eight-coordinated and bonded to the sulfoxide moieties via the oxygen atom.
    报道了La(ClO 4)3和十一种具有式RS(O)(CH 2)x S(O)R的二亚砜之间的配合物的合成和表征。在所有情况下,镧离子都是八配位的,并通过氧原子键合至亚砜部分。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Sc: MVol.D4, 1.1.16, page 45 - 46
    作者:
    DOI:——
    日期:——
  • Bidentate Sulfoxide Complexes of Ruthenium(II) and Their Preliminary Biological Assessment <i>in Vitro</i>
    作者:Donald T. T. Yapp、Steven J. Rettig、Brian R. James、Kirsten A. Skov
    DOI:10.1021/ic9606486
    日期:1997.11.1
    The complexes trans-RuCl2(BMSE)(2) (1), cis-RuCl2(BESE)(2) (2), trans-RuCl2(BPSE)(2) (3), and cis-RuCl2(BMSP)(2) (4) have been synthesized and characterized, including X-ray analyses [BMSE = 1,2-bis(methylsulfinyl)ethane, BESE = 1,2-bis(ethylsulfinyl)ethane, BPSE = 1,2-bis(propylsulfinyl)ethane, and BMSP = 1,3-bis(methylsulfinyl)propane]. Crystal data are as follows: 1 . H2O, triclinic, P1, a 8.863(1) Angstrom, b = 14.462(3) Angstrom, c 7.543(1) Angstrom, alpha = 103.39(1)degrees, beta = 113.31(1)degrees, gamma = 77.23(1)degrees, 2=2; 2 . MeOH, triclinic, , n 14.858(2) Angstrom, b = 16.732(3) Angstrom, c 10.609(2) Angstrom, alpha 105.14(2)degrees, beta 93.34(2)degrees, gamma = 115.91(1)degrees, Z= 4; 3, orthorhombic, Aba2, a = 14.894(1) Angstrom, b = 7.501(1) Angstrom, c = 21.911(2) Angstrom, Z = 4; 4, orthorhombic, Pcab, a = 15.257(3) Angstrom, b = 18.138(2) Angstrom, c = 13.395(2) Angstrom, Z = 8. The structures were solved by the Patterson method and were refined by full-matrix least-squares procedures to R = 0.026, 0.026, 0.029, and 0.031 for 10461, 8952, 1594, and 5694 reflections with I > 3 sigma(I), for 1-4, respectively. Preliminary in vitro experiments with Chinese hamster ovary cells indicate that the trans-complexes accumulate in the cells and bind to DNA to a greater degree than the cis-complexes.
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