摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(phenylthio)malononitrile | 30866-13-8

中文名称
——
中文别名
——
英文名称
(phenylthio)malononitrile
英文别名
Phenylthiomalonitril;2-Phenylsulfanylpropanedinitrile
(phenylthio)malononitrile化学式
CAS
30866-13-8
化学式
C9H6N2S
mdl
——
分子量
174.226
InChiKey
YCTSGLALDQMZEJ-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    72.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    活性亚甲基化合物与磺胺的磺酰化
    摘要:
    衍生自仲烷基胺的次磺酰胺与活性亚甲基化合物的等摩尔反应以良好的产率提供单次磺酰化的化合物。2 mol 衍生自酰亚胺的次磺酰胺与 1 mol 活性亚甲基化合物在碱存在下反应,得到二亚磺酰化化合物。发现α-单-亚磺酰化酮是通过烯胺与衍生自酰亚胺的次磺酰胺反应制备的。α-gem-Di-sulfenylated 酮是通过 α-mono-sulfenylated 酮与衍生自酰亚胺的亚磺酰胺在碱存在下反应制备的。还研究了N-苯基硫代苯甲脒盐酸盐的制备和反应。
    DOI:
    10.1246/bcsj.45.866
点击查看最新优质反应信息

文献信息

  • Pyrolysis of (2-Phenylethyl)phenylsulfonium Ylides.
    作者:Toshiaki Yoshimura、Atsushi Motoyama、Akiko Morishige、Eiichi Tsukurimichi、Choichiro Shimasaki、Kiyoshi Hasegawa
    DOI:10.1246/bcsj.66.174
    日期:——
    In order to obtain information concerning the reaction mechanism of the pyrolysis of sulfonium ylides bearing a substituted phenyl group on the 2-position in the S-ethyl group of ethylphenylsulfonium ylide, (2-phenylethyl)phenylsulfonium bis(methoxycarbonyl)methylide (1) and dicyanomethylide (2) were subjected to pyrolysis in benzene. The reaction rates of 1 and 2 at 140 °C were 6.0- and 3.2-times faster than those of ethylphenylsulfonium bis(methoxycarbonyl)methylide and dicyanomethylide, respectively. The activation parameters for 1 were ΔH‡ = 125 kJ mol−1 and ΔS‡ = −3.8 J K−1 mol−1, while those for 2 were ΔH‡ = 124 kJ mol−1 and ΔS‡ = −2.5 J K−1 mol−1. Substituent effects on the β-phenyl groups in 1 and 2 afforded positive Hammett ρ-values: ρ = 0.49 (γ = 0.997) and ρ = 0.26 (γ = 0.993), respectively.From the obtained results, it was suggested that the pyrolysis proceeds through essentially a concerted intramolecular cis-elimination inclined toward a slightly carbanion-like type from an E1-like type by introducing a phenyl substituent at the 2-position of the ethyl group in the ethylphenylsulfonium ylide.
    为了获取有关乙基苯基亚磺酸乙酯中乙基的2-位上带有取代基的磺酸磺酸分解反应机理的信息,将(2-乙基)基亚磺酸双(甲基羰基)甲亚基(1)和双基甲亚基(2)在中进行分解。在140°C时,1和2的反应速率分别比乙基苯基亚磺酸双(甲基羰基)甲亚基和双基甲亚基快6.0倍和3.2倍。1的活化参数为ΔH‡ = 125 kJ mol−1,ΔS‡ = -3.8 J K−1 mol−1,而2的活化参数为ΔH‡ = 124 kJ mol−1,ΔS‡ = -2.5 J K−1 mol−1。1和2中β-基的取代效应提供了正的Hammett ρ值:ρ = 0.49(γ = 0.997)和ρ = 0.26(γ = 0.993)。从得到的结果可以看出,通过在乙基苯基亚磺酸乙的乙基的2-位引入基取代基,基本上是通过倾向于稍微类似于负离子的顺式消除过程,从而类似于E1型反应。
  • Regioselective Mono- and Bis-Sulfenylation of Active Methylene Compounds
    作者:Namita Devi、Rajjakfur Rahaman、Kuladip Sarma、Pranjit Barman
    DOI:10.1002/ejoc.201501148
    日期:2016.1
    Selective mono- and bis-sulfenylation of active methylene groups with a variety of disulfides at an ambient temperature is reported. Sulfenylation is promoted by iodine as a catalyst and sulfenyl iodides as intermediates, under metal-free conditions. The method is greener in terms of solvent selection and the use of less hazardous DMSO as an oxidant. The procedure is highly efficient with readily available
    据报道,在环境温度下,活性亚甲基与多种二硫化物的选择性单-和双-亚磺酰化反应。在无属条件下,以催化剂,以亚中间体,可促进亚磺酰化。该方法在溶剂选择和使用危害较小的 DMSO 作为化剂方面更环保。该程序非常有效,使用容易获得的起始材料,并提供良好的收率。
  • Metal free sulfenylation of active methylene compounds and indole: TBATB mediated synthesis
    作者:Rajjakfur Rahaman、Namita Devi、Pranjit Barman
    DOI:10.1016/j.tetlet.2015.05.062
    日期:2015.7
    The present work addresses a development of metal free one pot direct method for sulfenylation of active methylene compounds and indole. The reaction might proceed through sulfenyl bromide as an intermediate, which initiates the C-S bond formation. The reaction was performed using tetrabutylammonium tribromide (TBATB) as a brominating agent, CH2Cl2 as a solvent at room temperature. (C) 2015 Elsevier Ltd. All rights reserved.
  • Yoshimura, Toshiaki; Motoyama, Atsushi; Kitada, Tomoko, Phosphorus, Sulfur and Silicon and the Related Elements, 1992, vol. 71, # 1-4, p. 85 - 92
    作者:Yoshimura, Toshiaki、Motoyama, Atsushi、Kitada, Tomoko、Tsukurimichi, Eiichi、Simasaki, Choichoiro、Hasegawa, Kiyoshi
    DOI:——
    日期:——
  • COMPOSITIONS, KITS AND RELATED METHODS FOR THE DETECTION AND/OR MONITORING OF LISTERIA
    申请人:GEN-PROBE INCORPORATED
    公开号:US20170211132A1
    公开(公告)日:2017-07-27
    Provided are compositions, kits, and methods for the identification of Listeria. In certain aspects and embodiments, the compositions, kits, and methods may provide improvements in relation to specificity, sensitivity, and speed of detection.
查看更多

同类化合物

(Rp)-2-(叔丁硫基)-1-(二苯基膦基)二茂铁 (1E)-1-{4-[(4-氨基苯基)硫烷基]苯基}乙酮肟 颜料红88 颜料紫36 顺式-1,2-二(乙硫基)-1-丙烯 非班太尔-D6 雷西那得中间体 阿西替尼杂质J 阿西替尼杂质C 阿西替尼杂质4 阿西替尼杂质 阿西替尼 阿拉氟韦 阿扎毒素 阿嗪米特 阔草特 银(I)(6-氨基-2-(甲硫基)-5-亚硝基嘧啶-4-基)酰胺水合物 钾三氟[3-(苯基硫基)丙基]硼酸酯(1-) 邻甲苯基(对甲苯基)硫化物 避虫醇 连翘脂苷B 还原红 41 还原紫3 还原桃红R 达索尼兴 辛硫醚 辛-1,7-二炔-1-基(苯基)硫烷 西嗪草酮 萘,2-[(2,3-二甲基苯基)硫代]- 莫他哌那非 茴香硫醚 苯醌B 苯酰胺,N-(氨基亚氨基甲基)-4-[(2-甲基苯基)硫代]-3-(甲磺酰)-,盐酸盐 苯酰胺,N-(氨基亚氨基甲基)-4-[(2-氯苯基)硫代]-3-(甲磺酰)-,盐酸盐 苯酰胺,N-(氨基亚氨基甲基)-4-[(2,6-二氯苯基)硫代]-3-(甲磺酰)-,盐酸盐 苯酰胺,2-[(2-硝基苯基)硫代]- 苯酚,3-氯-4-[(4-硝基苯基)硫代]- 苯酚,3-(乙硫基)- 苯酚,3,5-二[(苯基硫代)甲基]- 苯胺,4-[5-溴-3-[4-(甲硫基)苯基]-2-噻嗯基]- 苯胺,3-氯-4-[(1-甲基-1H-咪唑-2-基)硫代]- 苯胺,2-[(2-吡啶基甲基)硫代]- 苯硫醚-D10 苯硫胍 苯硫基乙酸 苯硫代磺酸S-(三氯乙烯基)酯 苯甲醇,2,3,4,5,6-五氟-a-[(苯基硫代)甲基]-,(R)- 苯甲酸,3-[[2-[(二甲氨基)甲基]苯基]硫代]-,盐酸 苯甲胺,5-氟-2-((3-甲氧苯基)硫代)-N,N-二甲基-,盐酸 苯甲二硫酸,4-溴苯基酯