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trans-1,4-bis(phenylsulfanyl)-2-buene | 6728-08-1

中文名称
——
中文别名
——
英文名称
trans-1,4-bis(phenylsulfanyl)-2-buene
英文别名
trans-1,4-bis(phenylthio)-2-butene;1,4-bis(phenylthio)-2-butene;1,4-bis-phenylsulphide-but-2-ene;1,4-Diphenylthio-2-buten;1,4-bis-phenylsulfanyl-but-2t-ene;1,4-Bis-phenylmercapto-but-2t-en;1,4-Dithiophenoxy-but-2t-en;[(E)-4-phenylsulfanylbut-2-enyl]sulfanylbenzene
trans-1,4-bis(phenylsulfanyl)-2-buene化学式
CAS
6728-08-1
化学式
C16H16S2
mdl
——
分子量
272.435
InChiKey
FJZPSPBGUQSOQX-BQYQJAHWSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为反应物:
    参考文献:
    名称:
    Everhardus,R.H. et al., Recueil des Travaux Chimiques des Pays-Bas, 1974, vol. 93, p. 90 - 91
    摘要:
    DOI:
  • 作为产物:
    描述:
    烯丙氧基苯硫酚 在 ruthenium(tricyclohexyl phosphane)(CHCHC(CH3)2)(C3H2N2(mesityl)2)Cl2 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以84%的产率得到trans-1,4-bis(phenylsulfanyl)-2-buene
    参考文献:
    名称:
    Allyl sulphides in olefin metathesis: catalyst considerations and traceless promotion of ring-closing metathesis
    摘要:
    烯丙基硫醚与适当的催化剂配对时会引发快速的烯烃转化反应。在中继转化中,烯丙基硫醚可以作为无痕催化剂,促进非硫化物目标的合成。
    DOI:
    10.1039/c4cc07932a
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文献信息

  • RECORDING MATERIAL PRODUCED USING NON-PHENOL COMPOUND
    申请人:NIPPON SODA CO., LTD.
    公开号:US20150284321A1
    公开(公告)日:2015-10-08
    An object of the present invention is to provide a recording material or a recording sheet using, as a color-developing agent, a non-phenol compound that is a safe compound in no danger of corresponding to an endocrine disruptor and is good in color developing performance. The non-phenol compound used in the present invention is at least one selected from the group consisting of compounds represented by the following formulas (I) to (III).
    本发明的目的是提供一种使用非酚类化合物作为显色剂的记录材料或记录纸,该非酚类化合物是一种安全化合物,不会对应到内分泌干扰物,并且在显色性能方面表现良好。本发明中使用的非酚类化合物至少选自以下化合物所代表的化合物组,其化学式为(I)至(III)。
  • N-Heterocyclic Carbene Complexes Of Metal Imido Alkylidenes And Metal OXO Alkylidenes, And The Use Of Same
    申请人:UNIVERSITÄT STUTTGART
    公开号:US20170050994A1
    公开(公告)日:2017-02-23
    The invention relates to an N-heterocyclic carbene complex of general formulas I to IV (I) (II) (III) (IV), according to which A1 stands for NR2 or PR2, A2 stands for CR2 R2′, NR2, PR2, 0 or S, A3 stands for N or P, and C stands for a carbene carbon atom, ring B is an unsubstituted or a mono or poly-substituted 5 to 7-membered ring, substituents R2 and R2′ stand, inter alia, for a linear or branched C1-Cw-alkyl group and, if N and N each stand for NR2 or PR2, are the same or different, M in formulas I, II, III or IV stands for Cr, Mo or W, X 1 or X2 in formulas I to IV are the same or different and represent, inter alia, C1-C1s carboxylates and C1-C1s-alkoxides, Y is inter alia oxygen or sulphur, Z is inter alia a linear or branched C1-Cw-alkylenoxy group, and R 1 and R1′ in formulas I to IV are, inter alia, an aliphatic or aromatic group. These compounds are particularly suitable for use as catalysts for olefin metathesis reactions and have the advantage, compared to known Schrock carbene complexes, of displaying clearly increased tolerance to functional groups such as, in particular, aldehydes, secondary amines, nitriles, carboxylic acids and alcohols.
    该发明涉及一种N-杂环卡宾复合物,其一般公式为I至IV(I)(II)(III)(IV),其中A1代表NR2或PR2,A2代表CR2R2′,NR2,PR2,0或S,A3代表N或P,C代表卡宾碳原子,环B为未取代或单取代或多取代的5至7元环,取代基R2和R2′代表线性或支链的C1-Cw-烷基基团,如果N和N分别代表NR2或PR2,则它们可以相同也可以不同,公式I、II、III或IV中的M代表Cr、Mo或W,公式I至IV中的X1或X2是相同或不同的,代表C1-C1s羧酸盐和C1-C1s-烷氧基等,Y为氧或硫等,Z为线性或支链的C1-Cw-烷氧基基团等,公式I至IV中的R1和R1′为脂肪族或芳香族基团等。这些化合物特别适用作为烯烃重排反应的催化剂,并相比已知的Schrock卡宾复合物,具有明显增强的对官能团的耐受性,特别是对醛、二级胺、腈、羧酸和醇等的耐受性增强。
  • Cationic Tungsten Imido Alkylidene N-Heterocyclic Carbene Complexes That Contain Bulky Ligands
    作者:Roman Schowner、Janis V. Musso、Wolfgang Frey、Michael R. Buchmeiser
    DOI:10.1021/acs.organomet.1c00373
    日期:2021.9.27
    Neutral and cationic tungsten imido alkylidene complexes of the general formulas W(NtBu)(CHR1)(OR2)Cl(NHC), W(N-2,6-bis(2,4,6-tri-iPr-C6H4)phenyl)(CHR1)Cl2(NHC), [W(NtBu)(CHR1)(OR2)(NHC)][B(ArF)4] and [W(N-2,6-bis(2,4,6-tri-iPr-C6H4)phenyl)(CHR1)Cl(NHC)][B(ArF)4] (R1 = CMe3, CMe2Ph; R2 = sterically demanding alkoxide; B(ArF)4 = tetrakis(3,5-(CF3)2-C6H3)borate; NHC = N-heterocyclic carbene) were prepared
    通式 W( Nt Bu)(CHR 1 )(OR 2 )Cl(NHC), W( N -2,6-bis(2,4,6- tri - i Pr- C 6 H 4 )苯基)(CHR 1 )Cl 2 (NHC)、[W( Nt Bu)(CHR 1 )(OR 2 )(NHC)][B(Ar F ) 4 ]和[W( N -2) ,6-双(2,4,6-三-i Pr-C 6 H 4 )苯基)(CHR 1 )Cl(NHC)][B(Ar F ) 4 ] (R 1 = CMe3、CMe 2 Ph;R 2 = 空间要求高的醇盐;B(Ar F ) 4 = 四(3,5-(CF 3 ) 2 -C 6 H 3 )硼酸盐;NHC = N-杂环卡宾)。两种电子不同的 NHC,即 1,3-二甲基咪唑-2-亚基 (IMe) 和 1,3-二甲基-4,5-二氯咪唑-2-亚基 (IMeCl),以及多种三酚盐和手性双酚盐受雇。在 1-十二烯的 HM
  • Organic synthesis with reagents derived from 3R3SiMgMe and MnCl2
    作者:Keigo Fugami、Jun-ichi Hibino、Shigeki Nakatsukasa、Seijiro Matsubara、Koichiro Oshima、Kiitiro Utimoto、Hitosi Nozaki
    DOI:10.1016/s0040-4020(01)86672-2
    日期:1988.1
    R3SiMgMe and MnCl2 are disclosed. (1) The manganese species reacted with terminal acetylenes to give 1,2-disilylated 1-alkenes. Mono- and bis(trimethylsilyl) acetylenes gave tri- and tetrasilylated ethenes, respectively, in good yields. Highly strained tetrakis(trimethylsilyl) ethene has now become easily accessible by this technique. (2) The reaction of alkenyl halides, alkenyl sulfides, and enol phosphates
    由3个当量衍生的试剂介导的合成上有用的反应。R 3 SiMgMe和MnCl 2的合成被披露。(1)锰与末端乙炔反应生成1,2-二甲硅烷基化的1-烯烃。单和双(三甲基甲硅烷基)乙炔分别以高收率得到三和四甲硅烷基化的乙烯。现在,通过这种技术可以轻松获得高应变四(三甲基甲硅烷基)乙烯。(2)链烯基卤化物,链烯基硫化物和烯醇磷酸盐与标题试剂的反应提供了高产率的乙烯基硅烷。该方法也适用于由烯丙基硫化物和醚合成烯丙基硅烷。(3)用锰试剂处理1,3-二烯提供了甲硅烷基化的烯丙基锰化合物,其以高的区域选择性加到羰基部分上。
  • New syntheses of vinylsilanes and allylsilanes by cross-coupling of (R3Si)3MnMgMe with alkenyl and allylic compounds
    作者:Keigo Fugami、Koichiro Oshima、Kiitiro Utimoto、Hitosi Nozaki
    DOI:10.1016/s0040-4039(00)84475-5
    日期:1986.1
    The reaction of alkenyl halides, alkenyl sulfides, and enol phosphates with (R3Si)3MnMgMe provides vinylsilanes in good yields. The method is also applicable to the allylsilane synthesis from allylic sulfides and ethers.
    链烯基卤化物,链烯基硫化物和烯醇磷酸盐与(R 3 Si)3 MnMgMe的反应以良好的产率提供了乙烯基硅烷。该方法也适用于由烯丙基硫化物和醚合成烯丙基硅烷。
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