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1,5-anhydro-6-O-octadecanoyl-D-fructose | 252977-30-3

中文名称
——
中文别名
——
英文名称
1,5-anhydro-6-O-octadecanoyl-D-fructose
英文别名
1,5-Anhydro-6-O-stearoyl-D-fructose;[(2R,3S,4S)-3,4-dihydroxy-5-oxooxan-2-yl]methyl octadecanoate
1,5-anhydro-6-O-octadecanoyl-D-fructose化学式
CAS
252977-30-3
化学式
C24H44O6
mdl
——
分子量
428.61
InChiKey
SCDADWACVUHUKY-GMKZXUHWSA-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):
    6.8
  • 重原子数:
    30
  • 可旋转键数:
    19
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    93.1
  • 氢给体数:
    2
  • 氢受体数:
    6

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:
    描述:
    1,5-anhydro-6-O-octadecanoyl-D-fructose盐酸羟胺 作用下, 以 吡啶 为溶剂, 反应 1.0h, 生成 1,5-anhydro-6-O-octadecanoyl-D-fructose oxime
    参考文献:
    名称:
    1,5-Anhydro-d-fructose: regioselective acylation with fatty acids
    摘要:
    Regioselective acylation of 1,5-anhydro-D-fructose was performed with dodecanoic acid to give 1,5-anhydro-6-O-dodecanoyl-D-fructose, chemically in 50% yield and enzymatically in quantitative yield. Quantitative conversions were also obtained using hexadecanoic and octadecanoic acids as acyl donors. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(99)00163-9
  • 作为产物:
    描述:
    1,5-脱水-d-果糖硬脂酸 在 3 A molecular sieve 、 Novorym 435 作用下, 以 丙酮 为溶剂, 反应 168.0h, 以65%的产率得到1,5-anhydro-6-O-octadecanoyl-D-fructose
    参考文献:
    名称:
    1,5-Anhydro-d-fructose: regioselective acylation with fatty acids
    摘要:
    Regioselective acylation of 1,5-anhydro-D-fructose was performed with dodecanoic acid to give 1,5-anhydro-6-O-dodecanoyl-D-fructose, chemically in 50% yield and enzymatically in quantitative yield. Quantitative conversions were also obtained using hexadecanoic and octadecanoic acids as acyl donors. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(99)00163-9
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文献信息

  • 1,5-Anhydro-D-fructose substituted with a hydrophobic group for use as anti-oxidant and/or emulsifier
    申请人:——
    公开号:US20020102342A1
    公开(公告)日:2002-08-01
    The present invention provides a derivatised anhydrofructose comprising a hydrophobic group linked (directly or indirectly) to a C of an anhydrofructose moiety.
    本发明提供了一种衍生化的无水果糖,其包含一个疏水基团与无水果糖基团上的碳(直接或间接)连接。
  • 1,5-ANHYDRO-D-FRUCTOSE SUBSTITUTED WITH A HYDROPHOBIC GROUP FOR USE AS ANTI-OXIDANT AND/OR EMULSIFIER
    申请人:DANISCO A/S
    公开号:EP1163248B1
    公开(公告)日:2004-09-22
  • [EN] 1,5-ANHYDRO-D-FRUCTOSE SUBSTITUTED WITH A HYDROPHOBIC GROUP FOR USE AS ANTI-OXIDANT AND/OR EMULSIFIER<br/>[FR] 1,5-ANHYDRO-D-FRUCTOSE SUBSTITUEE PAR UN GROUPE HYDROPHOBE, SERVANT D'ANTI-OXYDANT ET/OU D'EMULSIFIANT
    申请人:DANISCO
    公开号:WO2000056745A1
    公开(公告)日:2000-09-28
    There is provided a derivatised anhydrofructose comprising a hydrophobic group linked (directly or indirectly) to a C of an anhydrofructose moiety.
  • 1,5-Anhydro-d-fructose: regioselective acylation with fatty acids
    作者:Søren M Andersen、Inge Lundt、Jan Marcussen、Shukun Yu
    DOI:10.1016/s0008-6215(99)00163-9
    日期:1999.8
    Regioselective acylation of 1,5-anhydro-D-fructose was performed with dodecanoic acid to give 1,5-anhydro-6-O-dodecanoyl-D-fructose, chemically in 50% yield and enzymatically in quantitative yield. Quantitative conversions were also obtained using hexadecanoic and octadecanoic acids as acyl donors. (C) 1999 Elsevier Science Ltd. All rights reserved.
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