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methyl 2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-α-D-altopyranoside | 1030028-15-9

中文名称
——
中文别名
——
英文名称
methyl 2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-α-D-altopyranoside
英文别名
——
methyl 2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-α-D-altopyranoside化学式
CAS
1030028-15-9
化学式
C32H52O6Si2
mdl
——
分子量
588.932
InChiKey
OCYXWFPUGWCJFV-ZNOUKXQUSA-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

物化性质

  • 沸点:
    600.1±55.0 °C(predicted)
  • 密度:
    1.07±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.07
  • 重原子数:
    40.0
  • 可旋转键数:
    11.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    77.38
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

上下游信息

  • 下游产品
    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:
    methyl 2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-α-D-altopyranoside三苯基氯甲烷4-二甲氨基吡啶 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以93%的产率得到methyl 2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-6-O-(triphenylmethyl)-α-D-altropyranoside
    参考文献:
    名称:
    The 2α-(3-hydroxypropyl) group as an active motif in vitamin D3 analogues as agonists of the mutant vitamin D receptor (Arg274Leu)
    摘要:
    We designed and synthesized 1 alpha- and 1 beta-hydroxymethyl-2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (2a,b) and related analogues 2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (3), Posner's analogues of 1 alpha- and 1 beta-hydroxymethyl-25-hydroxyvitamin D-3 (4a,b), as well as 2 alpha-(3-hydroxypropyl)-1 alpha,25-dihydroxyvitamin D-3 (5), to confirm the effect of the 1 alpha-hydroxy group and/or 2 alpha-(3-hydroxypropyl) group of vitamin D-3 analogues with the modified A-ring moiety on the mutant vitamin D receptor, VDR(Arg274Leu). The 2 alpha-(3-hydroxypropyl) group showed better effect on enhancement of the transcriptional activity through the mutant VDR than the 1 alpha- and 1 beta-hydroxymethyl groups. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.039
  • 作为产物:
    描述:
    methyl 4,6-O-benzylidene-2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-α-D-altopyranosidelithium 作用下, 以 四氢呋喃 为溶剂, 反应 0.25h, 以95%的产率得到methyl 2-O-(tert-butyldimethylsilyl)-3-C-{3-(tert-butyldiphenylsilyloxy)propyl}-3-deoxy-α-D-altopyranoside
    参考文献:
    名称:
    The 2α-(3-hydroxypropyl) group as an active motif in vitamin D3 analogues as agonists of the mutant vitamin D receptor (Arg274Leu)
    摘要:
    We designed and synthesized 1 alpha- and 1 beta-hydroxymethyl-2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (2a,b) and related analogues 2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (3), Posner's analogues of 1 alpha- and 1 beta-hydroxymethyl-25-hydroxyvitamin D-3 (4a,b), as well as 2 alpha-(3-hydroxypropyl)-1 alpha,25-dihydroxyvitamin D-3 (5), to confirm the effect of the 1 alpha-hydroxy group and/or 2 alpha-(3-hydroxypropyl) group of vitamin D-3 analogues with the modified A-ring moiety on the mutant vitamin D receptor, VDR(Arg274Leu). The 2 alpha-(3-hydroxypropyl) group showed better effect on enhancement of the transcriptional activity through the mutant VDR than the 1 alpha- and 1 beta-hydroxymethyl groups. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.039
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