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(S)-3,4-dimethyl-5-oxo-2-pentyl-2,5-dihydrofuran-2-yl acetate | 1496537-31-5

中文名称
——
中文别名
——
英文名称
(S)-3,4-dimethyl-5-oxo-2-pentyl-2,5-dihydrofuran-2-yl acetate
英文别名
——
(S)-3,4-dimethyl-5-oxo-2-pentyl-2,5-dihydrofuran-2-yl acetate化学式
CAS
1496537-31-5
化学式
C13H20O4
mdl
——
分子量
240.299
InChiKey
WQAGLCVTDPJYMQ-ZDUSSCGKSA-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

反应信息

  • 作为产物:
    描述:
    (S)-5-hydroxy-3,4-dimethyl-5-pentylfuran-2(5H)-one 、 乙酸酐吡啶 作用下, 反应 20.0h, 以2.5 mg的产率得到(S)-3,4-dimethyl-5-oxo-2-pentyl-2,5-dihydrofuran-2-yl acetate
    参考文献:
    名称:
    Isolation of a new butenolide from the South China Sea gorgonian coral Subergorgia suberosa
    摘要:
    Chemical investigation on the South China Sea gorgonian coral Subergorgia suberosa has led to the isolation of one new butenolide (5R)-5-(1-ethoxypropyl)-5-hydroxy-3,4-dimethylfuran-2(5H)-one (1) as a pair of inseparable epimers, along with two known butenolides (S)-5-hydroxy-3,4-dimethyl-5-propylfuran-2(5H)-one (2) and (S)-5-hydroxy-3,4-dimethyl-5-pentylfuran-2(5H)-one (3). Their structures including absolute configurations were determined unambiguously by detailed analyses of spectroscopic data and by comparison with the available literature. Compounds 1-3 exhibited moderate antifouling activities against the settlement of Balanus amphitrite larvae, whereas compound 4, the acetyl derivative of 3, showed no antifouling activity at the concentrations up to 25g/mL.
    DOI:
    10.1080/14786419.2013.857668
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