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tert-butylsulfanyl tributyltin | 23728-82-7

中文名称
——
中文别名
——
英文名称
tert-butylsulfanyl tributyltin
英文别名
Tributylstannyl tert-butyl sulfide;tributyl(tert-butylthio)stannane;Tri-n-butylzinn-tert-butylmercaptid;(n-Bu)3SnS(t-Bu);tributyl[(1,1-dimethylethyl)thio]stannane;(tert-butylsulphanyl)tributyltin;tributyl(tert-butylsulfanyl)stannane
tert-butylsulfanyl tributyltin化学式
CAS
23728-82-7
化学式
C16H36SSn
mdl
——
分子量
379.238
InChiKey
DJWNZDKJIDCCJA-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

物化性质

  • 沸点:
    110 °C(Press: 0.1 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    6.86
  • 重原子数:
    18
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    25.3
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:9990f0c5a2cd6e73c1422690bb464401
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反应信息

  • 作为反应物:
    描述:
    [RuCl(CO)(PPh3)(η-C5H5)] 、 tert-butylsulfanyl tributyltin甲醇 为溶剂, 以19%的产率得到
    参考文献:
    名称:
    The synthesis of several new cyclopentadienyl-ruthenium t-butyl thiol complexes
    摘要:
    The air-sensitive complexes [CpRu(L)(L')(HSBu(t)]PF6 (L = L' = PPh(OMe)2, PPh2OMe, P(OMe)3; L = PPh3, L' = CO, P(OMe)3) are prepared by heating methanol solutions of CpRu(L)(L')Cl, HSBu(t), and NH4PF6. The cyclopentadienyl-ruthenium thiol complexes oxidized in air to form paramagnetic complexes, one of which, [CpRu(PPh2OMe)2SBu(t)]PF6, was isolated and characterized by a single crystal x-ray diffraction study. Crystals are monoclinic with space group P2(1)/c, a = 12.8070(25), b = 14.3160(36), c = 20.1768(50) angstrom, beta = 97.841(18)-degrees, and Z = 4. Data were refined to R = 0.0452 (6248 reflections). The Ru-S(1) bond length was 2.274(1) angstrom and the Ru-P bond lengths were 2.298(1) and 2.291(1) angstrom. The synthesis of CpRu(CO)(PPh3)SBu(t) is also reported.
    DOI:
    10.1016/0022-328x(91)86205-5
  • 作为产物:
    描述:
    叔丁基硫醇三丁基氧化锡甲苯 为溶剂, 以80%的产率得到tert-butylsulfanyl tributyltin
    参考文献:
    名称:
    Thunecke, Frank; Schulze, Dirk; Borsdorf, Rolf, Zeitschrift fur Chemie, 1990, vol. 30, p. 444 - 445
    摘要:
    DOI:
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文献信息

  • Facile preparation of thiol esters from organotin mercaptides and acyl chlorides
    作者:David N. Harpp、T. Aida、T.H. Chan
    DOI:10.1016/s0040-4039(01)86433-9
    日期:——
    Organotin mercaptides condense with acyl chlorides to give thiol esters in excellent yield. Of note are efficient syntheses of -butyl and phenyl thiol esters.
    有机锡硫醇盐与酰氯缩合,以优异的收率得到硫醇酯。值得注意的是-丁基和苯基硫醇酯的有效合成。
  • Synthesis and reactivity of rhenium carbonyl thiolate complexes, Et4N[Re2(μ-SR)3(CO)6]
    作者:P.M. Treichel、M.H. Tegen
    DOI:10.1016/0022-328x(88)87088-8
    日期:1988.12
    Compounds of the formula Et4N[Re2(μ-SR)3(CO)6], (R  Me, But, Ph, C6F5) may be prepared in good yields from reactions between various halocarbonylrhenate anions and either the thiolate anion or (n-Bu)3SnSR. These stable, white or off-white, Crystalline species undergo reactions with [Me3O]BF4 in the presence of phosphines to form cis-Re2(μ-SR)2(CO)6(L)2 (L  PMe3, PPh3, 12 dppm). When heated in benzene
    式Et 4 N [Re 2(μ-SR)3(CO)6 ],(RMe,Bu t,Ph,C 6 F 5)的化合物可以由各种卤代羰基金属酸根阴离子与硫醇根阴离子或(n-Bu)3 SnSR。这些稳定的白色或类白色结晶物质在膦存在下与[Me 3 O] BF 4反应,形成顺式-Re 2(μ-SR)2(CO)6(L)2(LPMe 3,PPH 3,12 dppm)。当在苯中加热时,这些化合物会转化为反式异构体。相反,当它们在四氢呋喃中加热时,一氧化碳会流失,并且会分离出Re 2(μ-SR)2(μ-CO)(CO)4(L)2物质。
  • SULFINYLAMINOBENZAMIDE AND SULFONYLAMINOBENZAMIDE DERIVATIVES
    申请人:Gilead Sciences, Inc.
    公开号:US20190359565A1
    公开(公告)日:2019-11-28
    Provided is a compound of Formula (I): wherein the variable groups are defined herein.
    提供的是一个化合物的化学式(I):其中变量基团在此处定义。
  • Palladium catalysed elaboration of codeine and morphine
    作者:Stephen G. Davies、Christopher J. Goodwin、Dirk Pyatt、Andrew D. Smith
    DOI:10.1039/b102581n
    日期:——
    Palladium catalysed coupling reactions of 6-O-tert-butyldimethylsilyl-1-bromocodeine and 6-O-tert-butyldimethylsilyl-3-trifluoromethylsulfonylmorphine allow a range of substituted analogues of codeine in the 1-position and morphine in the 3-position to be efficiently and selectively prepared.
    通过钯催化 6-O-叔丁基二甲基硅烷-1-溴可待因和 6-O-叔丁基二甲基硅烷-3-三氟甲基磺酰基吗啡的偶联反应,可以高效、选择性地制备一系列 1 位可待因和 3 位吗啡的取代类似物。
  • McMurry intermolecular cross-coupling between an ester and a ketone: scope and limitations
    作者:Stéphane Sabelle、Jérôme Hydrio、Eric Leclerc、Charles Mioskowski、Pierre-Yves Renard
    DOI:10.1016/s0040-4039(02)00617-2
    日期:2002.5
    were faced with the synthesis of sterically hindered benzylic enol ethers. This issue was solved via the use of an intermolecular McMurry cross-coupling between an ester and a ketone. In this article, together with the synthesis of the chemiluminescent probe, the scope and limitations of this low valent titanium based carboncarbon double bond formation are discussed.
    在关于合成用于检测硫醇的带有二氧杂环丁烷的化学发光探针的研究过程中,我们面临着位阻苄基烯醇醚的合成。通过使用酯和酮之间的分子间McMurry交叉偶联解决了这个问题。在本文中,连同化学发光探针的合成,讨论了这种低价钛基碳碳双键形成的范围和局限性。
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