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1-Thiophen-2-yl-ethanethione | 97564-65-3

中文名称
——
中文别名
——
英文名称
1-Thiophen-2-yl-ethanethione
英文别名
1-Thiophen-2-ylethanethione;1-thiophen-2-ylethanethione
1-Thiophen-2-yl-ethanethione化学式
CAS
97564-65-3
化学式
C6H6S2
mdl
——
分子量
142.246
InChiKey
PELPZJHHJQCQRL-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):
    1.8
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    60.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    苯乙酮1-Thiophen-2-yl-ethanethioneN-溴代丁二酰亚胺(NBS) 作用下, 以 为溶剂, 以75 %的产率得到2-(2-thienyl)-4-phenylthiazole
    参考文献:
    名称:
    Visible-light-induced C–S bond formation in the synthesis of 2,4-disubstituted thiazoles through cascade difunctionalization of acetophenone: a greener approach
    摘要:

    A novel approach for the synthesis of 2,4-disubstituted thiazoles from methyl aryl ketones, N-bromo-succinimide (NBS), and thioamide in water as a green reaction medium through visible-light irradiation is reported.

    DOI:
    10.1039/d4ob00096j
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文献信息

  • Mayer, R.; Hartenhauer, H.; Gruner, M., Journal fur praktische Chemie (Leipzig 1954), 1991, vol. 333, # 1, p. 35 - 40
    作者:Mayer, R.、Hartenhauer, H.、Gruner, M.
    DOI:——
    日期:——
  • A METHOD FOR PREPARING OPTICALLY ACTIVE CARBONYL COMPOUND
    申请人:ZHEJIANG NHU COMPANY LTD.
    公开号:US20180105477A1
    公开(公告)日:2018-04-19
    The present invention discloses a method for preparing optically active carbonyl compound, comprising the following steps: under the catalysis of chiral amine salt and transition metal catalysts, with hydrogen and catalytic amount of dihydropyridine compound as hydrogen source, use α, β-unsaturated aldehydes or α, β-unsaturated troponoid compounds to conduct asymmetric catalytic reaction to obtain the optically active carbonyl compound. This method comes in moderate reaction condition, simple operation, and catalytic amount of dihydropyridine compounds usage, the target product is easy to be separated and purified from the reaction system, and the metal catalyst can be recycled, it is economical.
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