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di(tert-butylsulfenyl)mercury | 3374-16-1

中文名称
——
中文别名
——
英文名称
di(tert-butylsulfenyl)mercury
英文别名
di(t-butylthio)mercury;2-methyl-propane-2-thiol; mercury bis-(2-methyl-propane-2-thiolate);2-Methyl-propan-2-thiol; Quecksilber-bis-(2-methyl-propan-2-thiolat);2-Methyl-propan-2-thiol; Quecksilber(II)-Verbindung;Quecksilber-bis-tert-butylmercaptid;Quecksilber-tert.-butyl-mercaptid
di(tert-butylsulfenyl)mercury化学式
CAS
3374-16-1
化学式
C8H18HgS2
mdl
——
分子量
378.953
InChiKey
QREOIABEXJFXOQ-UHFFFAOYSA-M
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):
    1.33
  • 重原子数:
    6.0
  • 可旋转键数:
    0.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

安全信息

  • 海关编码:
    2930909090

SDS

SDS:4776959d6323672d0978e86946400e0b
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反应信息

  • 作为反应物:
    描述:
    二(三氟甲基)亚膦酰碘di(tert-butylsulfenyl)mercury 以 neat (no solvent) 为溶剂, 生成 mercury(II) iodide
    参考文献:
    名称:
    摘要:
    Perfluoromethyl phosphorus and -arsenic compounds of the type (F3C)(2)EE'R (E = P, As; E' = S, Se, Te; R = organic group) are prepared either by dismutation (metathesis) of E-2(CF3)(4) with (RE')(2) or by reaction of the iodine compounds (F3C)(2)EI with mercury(II) organosulfanides Hg(SR)(2) and characterized by spectroscopic (H-1, F-19, P-31-NMR; IR; MS) as well as analytical investigations (C, H).
    DOI:
    10.1002/(sici)1521-3749(199912)625:12<2085::aid-zaac2085>3.3.co;2-j
  • 作为产物:
    描述:
    参考文献:
    名称:
    Rheinboldt; Mott; Motzkus, Journal fur praktische Chemie (Leipzig 1954), 1932, vol. <2>134, p. 274
    摘要:
    DOI:
  • 作为试剂:
    描述:
    N-benzyl-S-cyanothiohydroxylamine乙醚di(tert-butylsulfenyl)mercury 作用下, 生成 N-benzyl-2-methyl-propane-2-sulfenamide
    参考文献:
    名称:
    Peyron; Laplaine, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1948, vol. 227, p. 132
    摘要:
    DOI:
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文献信息

  • Synthesis of Thiol, Selenol, and Tellurol Esters by the Reaction of Organochalcogeno Mercurials with Acid Chlorides
    作者:Claudio C. Silveira、Antonio L. Braga、Enrique L. Larghi
    DOI:10.1021/om990589e
    日期:1999.11.1
    Thiol, selenol, and tellurol esters were prepared by the reaction of bis(organochalcogeno)mercurials with acid chlorides in chloroform or carbon tetrachloride and in the presence of tetrabutylammonium halides as catalysts.
    通过在氯仿四氯化碳中,在卤化四丁基的存在下,使双(有机碳氢基)与酰反应,制得醇,醇和的酯。
  • Endovascular Treatment of a Lenticulostriate Artery Aneurysm with N-butyl Cyanoacrylate
    作者:Ramiro Larrazabal、David Pelz、J. Max Findlay
    DOI:10.1017/s0317167100001426
    日期:2001.8
    Background:

    Aneurysms arising from lenticulostriate artery branches in moyamoya-type disease are challenging lesions to treat, due to their fragility and deep location. Surgery is difficult and endovascular options may be limited.

    Methods:

    A 57-year-old woman presented with a right ganglionic parenchymal hemorrhage due to a ruptured lenticulostriate artery aneurysm associated with ipsilateral middle cerebral artery occlusion. The aneurysm and parent feeding artery were occluded using endovascular injection of N-butyl cyanoacrylate.

    Results:

    The aneurysm was successfully obliterated and although some glue did enter the more distal middle cerebral artery, there was no change in the patient's neurologic status.

    Conclusion:

    In highly selected cases where lenticulostriate aneurysms cannot be directly accessed for surgery or endovascular coiling, obliteration with liquid acrylic glue may be considered as a therapeutic option.

    背景:在莫亚莫亚型疾病中,由皮孔状动脉分支产生的动脉瘤因其脆性和深部位置,治疗起来具有挑战性。方法:一名 57 岁的女性因枕叶动脉动脉瘤破裂导致右侧神经节实质出血,并伴有同侧大脑中动脉闭塞。结果:动脉瘤被成功堵塞,虽然一些胶进入了较远端大脑中动脉,但患者的神经状况没有发生变化。结论:在无法直接进入皮孔状动脉瘤进行手术或血管内卷曲的高选择性病例中,可以考虑使用液态丙烯酸堵塞动脉瘤作为一种治疗选择。
  • Syntheses and vibrational spectra of some tris(alkanethiolato)mercurate(II) complexes, and crystal structure of the Hexakis(methanethiolato)dimercurate(II) dianion
    作者:GA Bowmaker、IG Dance、BC Dobson、DA Rogers
    DOI:10.1071/ch9841607
    日期:——

    The complexes [cation] [Hg(SR)3](R = Me, cation = Et4N+; R = But, cation = Et4N+, Bu4N+, [N(Ph3P)2]+) have been prepared. The crystal structure of the methanethiolate complex shows that it contains centrosymmetric dinuclear anions [(MeS)2Hg(�-SMe)2Hg(SMe)2]2- with distorted tetrahedral geometry about the mercury atoms. Vibrational spectroscopic evidence suggests that this complex dissociates on dissolution in ethanol to give mononuclear [Hg(SMe)3]- species. The ButS- complexes appear to exist as mononuclear [Hg(SBut)3]- species both in the solid state and in solution. The metal-sulfur stretching frequencies are assigned for all of the complexes studied, and the vibrational spectra are discussed in terms of the structures of the complex anions involved. Crystal data for [(C2H5)4N]2Hg2(SCH3)6 : a 8.656(5), b gS130(6), c 12.368(8) �; α 102.16(4), β 105.51(4), γ 105.29(4)�; space group P1, Z 1, R 0.034, Rw 0.042.

    阳离子] 复合物 [Hg(SR)3](R = Me,阳离子 = Et4N+;R = But、 阳离子 = Et4N+、Bu4N+、[N(Ph3P)2]+) 的晶体结构。甲硫醇复合物的晶体结构显示,它含有中心对称的 复合物的晶体结构显示,它含有中心对称的双核 阴离子[(MeS)2Hg(�-SMe)2Hg(SMe)2]2-,以原子为中心呈扭曲的四面体几何形状。 几何形状。振动 光谱证据表明,该复合物在乙醇中溶解后会解离出单核 乙醇中溶解,生成单核 [Hg(SMe)3]-。 物种。ButS- 复合物似乎 单核[Hg(SBut)3]-物种。 在固态和溶液中都以单核 [Hg(SBut)3]- 物种的形式存在。所有配合物的伸展 频率,并根据所涉及的络阴离子的结构对振动光谱进行了讨论。 的结构进行了讨论。(C2H5)4N]2Hg2(SCH3)6的晶体数据 :a 8.656(5),b gS130(6),c 12.368(8); α 102.16(4),β 105.51(4),γ 105.29(4)。 0.034,Rw 0.042。
  • Reaction of arsenic, antimony, bismuth and sulfur fluorides with (t-butylthio) trimethylsilane
    作者:A.F. Janzen、O.C. Vaidya、C.J. Willis
    DOI:10.1016/0022-1902(81)80318-1
    日期:1981.1
    Tris(t-butylthio) derivatives of arsenic, antimony and bismuth have been prepared in high yield by the reaction of metal fluoride with (t-butylthio)trimethylsilane. The products have been characterized by elemental analysis, IR, Raman, proton NMR and mass spectrometry. Attempts to prepare As(V), Sb(V) or S(IV) derivatives were unsuccessful, although the reaction of SF4 or Et2NSF3 suggests the formation
    通过化物与(叔丁基基)三甲基硅烷的反应,高产率地制备了的三(叔丁基基)衍生物。产品已通过元素分析,IR,拉曼,质子NMR和质谱进行了表征。尽管SF 4或Et 2 NSF 3的反应表明形成了S(IV)中间体,但未能成功制备As(V),Sb(V)或S(IV)衍生物
  • Rheinboldt; Dewald; Diepenbruck, Journal fur praktische Chemie (Leipzig 1954), 1931, vol. <2>130, p. 138
    作者:Rheinboldt、Dewald、Diepenbruck
    DOI:——
    日期:——
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