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(1-formyl-propyl)-dimethyl-sulfonium betaine | 367926-59-8

中文名称
——
中文别名
——
英文名称
(1-formyl-propyl)-dimethyl-sulfonium betaine
英文别名
2-(Dimethyl-lambda4-sulfanylidene)butanal;2-(dimethyl-λ4-sulfanylidene)butanal
(1-formyl-propyl)-dimethyl-sulfonium betaine化学式
CAS
367926-59-8
化学式
C6H12OS
mdl
——
分子量
132.227
InChiKey
WUZDIJIYJBFJMC-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):
    0.5
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    36.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (1-formyl-propyl)-dimethyl-sulfonium betaine足球烯甲苯 为溶剂, 反应 20.0h, 以56%的产率得到2,2-[60]fullerenobutanal
    参考文献:
    名称:
    Synthesis and transformation of a novel methano[60]fullerene having a formyl group
    摘要:
    The reaction of [60]fullerene with a dimethylsulfonium alpha -formylalkylide gave a novel methano[60]fullerene having a formyl group at the bridge-head carbon, This 2.2-[60]fulleroalkanal was readily converted into a variety of N-aryl-2,2-[60]fulleroaldimines by condensation with aromatic amines: one of them showed efficient quenching of the fluorescence of the [60]fullerene core, due to a photoinduced intramolecular electron transfer. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)00944-3
  • 作为产物:
    描述:
    (α-formylpropyl)dimethylsulfonium tetrafluoroborate 在 sodium hydroxidepotassium carbonate 作用下, 以 氯仿 为溶剂, 以39%的产率得到(1-formyl-propyl)-dimethyl-sulfonium betaine
    参考文献:
    名称:
    Synthesis and transformation of a novel methano[60]fullerene having a formyl group
    摘要:
    The reaction of [60]fullerene with a dimethylsulfonium alpha -formylalkylide gave a novel methano[60]fullerene having a formyl group at the bridge-head carbon, This 2.2-[60]fulleroalkanal was readily converted into a variety of N-aryl-2,2-[60]fulleroaldimines by condensation with aromatic amines: one of them showed efficient quenching of the fluorescence of the [60]fullerene core, due to a photoinduced intramolecular electron transfer. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)00944-3
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文献信息

  • The Reactions of α-Substituted Carbonyl-stabilized Sulfonium Ylides with Succinic Anhydride
    作者:Teruaki Mukaiyama、Katsuaki Hagio、Hisashi Takei、Kazuhiko Saigo
    DOI:10.1246/bcsj.44.161
    日期:1971.1
    It was found that various kinds of α-substituted carbonyl-stabilized sulfonium ylides were conveniently prepared from the corresponding sulfonium salts by treating with 50% aqueous sodium hydroxide. The reactions of sulfonium ylides with succinic anhydride afforded furofuran derivative by one step procedure in yields ranging these from 5 to 14%. The structures of furofuran derivatives were confirmed
    结果表明,通过用 50% 氢氧化钠溶液处理相应的锍盐,可以方便地制备各种 α-取代的羰基稳定的锍叶立德。锍叶立德与琥珀酸酐的反应通过一步程序以 5% 至 14% 的产率提供呋喃生物。通过红外光谱、核磁共振谱、降解及其对碱和酸的行为证实了呋喃生物的结构。
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