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2-碘-1,3-丙二醇 | 5349-29-1

中文名称
2-碘-1,3-丙二醇
中文别名
——
英文名称
2-iodo-1,3-propanediol
英文别名
2-iodo-propane-1,3-diol;2-Jod-propan-1,3-diol;Glycerin-2-jodhydrin;Glycerin-β-jodhydrin;2-Jod-1.3-dihydroxy-propan;glycerol β-iodohydrin;2-Iodopropane-1,3-diol
2-碘-1,3-丙二醇化学式
CAS
5349-29-1
化学式
C3H7IO2
mdl
——
分子量
201.992
InChiKey
UQTRRWUQXIOVPL-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):
    -0.1
  • 重原子数:
    6
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:319460ef572b686a459fcf8d357199b4
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反应信息

  • 作为反应物:
    描述:
    2-碘-1,3-丙二醇雄诺龙对甲苯磺酸 作用下, 以 为溶剂, 生成
    参考文献:
    名称:
    Free radical macrocyclizations from steroid-derived precursors
    摘要:
    Stereoselective free radical addition reactions were studied using steroid-derived templates in an attempt to control product dispersity. Templates were prepared from bifunctional steroids appropriately substituted with initiating and terminating functionality. Free radical initiation in the presence of a polymerizable olefin resulted in the formation of macrocycles that had incorporated monomer. The yield of macrocycle formed was as high as 51 % for templates derived from lithocholic acid whereas templates derived from androstanolone failed to give significant amounts of macrocycles. The effects of variation of initiating and terminating functionality, steroid, and olefin on macrocycle size and yield were examined.
    DOI:
    10.1021/jo00057a034
  • 作为产物:
    描述:
    2-氯-1,3-丙二醇丙酮 、 sodium iodide 作用下, 生成 2-碘-1,3-丙二醇
    参考文献:
    名称:
    The C4-Saccharinic Acids. VI. Further Attempts to Prepare 2,2'-Dihydroxyisobutyric Acid. 2,3-Dihydroxybutyric Acid Lactone from Glycidol. The Preparation of the Two Iodohydrins of Glycerol1
    摘要:
    DOI:
    10.1021/ja01330a041
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文献信息

  • Structure-activity relationship of lipopeptide from outer membrane of Escherichia coli and synthesis of highly immunopotenting lipopeptide derivatives with an achiral lipo-part.
    作者:Muneaki KURIMURA、Kazuo ACHIWA
    DOI:10.1248/cpb.41.627
    日期:——
    For outstanding the structere-activity relationship of lipopeptide derivatives, high biologically active lipopeptide derivatives with an achiral lipo-part were newly synthesized
    为了突出脂肽衍生物的结构-活性关系,新近合成了具有非手性脂部分的生物活性高的脂肽衍生物
  • Hessel et al., Recueil des Travaux Chimiques des Pays-Bas, 1954, vol. 73, p. 842,846
    作者:Hessel et al.
    DOI:——
    日期:——
  • Petrov,K.A. et al., Journal of general chemistry of the USSR, 1961, vol. 31, p. 2692 - 2695
    作者:Petrov,K.A. et al.
    DOI:——
    日期:——
  • Hoefnagel,M.A. et al., Recueil des Travaux Chimiques des Pays-Bas, 1961, vol. 80, p. 608 - 622
    作者:Hoefnagel,M.A. et al.
    DOI:——
    日期:——
  • Verkade,P.E., Recueil des Travaux Chimiques des Pays-Bas, 1963, vol. 82, p. 450 - 452
    作者:Verkade,P.E.
    DOI:——
    日期:——
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