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2-(N-methylbenzamido)-5-(2-O,4-C-methylene-D-ribofuranosyl)thiazole | 1029931-26-7

中文名称
——
中文别名
——
英文名称
2-(N-methylbenzamido)-5-(2-O,4-C-methylene-D-ribofuranosyl)thiazole
英文别名
——
2-(N-methylbenzamido)-5-(2-O,4-C-methylene-D-ribofuranosyl)thiazole化学式
CAS
1029931-26-7
化学式
C17H18N2O5S
mdl
——
分子量
362.406
InChiKey
VWIAKAFBOKJCTF-WSMBLCCSSA-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):
    0.98
  • 重原子数:
    25.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    92.12
  • 氢给体数:
    2.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    2-(N-methylbenzamido)-5-(2-O,4-C-methylene-D-ribofuranosyl)thiazole4,4'-双甲氧基三苯甲基氯吡啶 为溶剂, 反应 12.0h, 以96%的产率得到2-(N-methylbenzamido)-5-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-D-ribofuranosyl]thiazole
    参考文献:
    名称:
    Recognition of T·A interruption by 2′,4′-BNAs bearing heteroaromatic nucleobases through parallel motif triplex formation
    摘要:
    2'-O,4'-C-methylene bridged nucleic acid (2',4'-BNA) monomers bearing novel unnatural nucleobases, 4-(3-benzamidophenyl)-2-pyridone and 2-(N-methylbenzamido)thiazole, were synthesized and successfully incorporated into oligonucleotides. UV melting experiments showed that the corresponding oligonucleotide derivatives formed stable triplexes with dsDNA targets even in the presence of a T center dot A interruption. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.043
  • 作为产物:
    描述:
    2-(N-methylbenzamido)-5-(3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranosyl)thiazole四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以72%的产率得到2-(N-methylbenzamido)-5-(2-O,4-C-methylene-D-ribofuranosyl)thiazole
    参考文献:
    名称:
    Recognition of T·A interruption by 2′,4′-BNAs bearing heteroaromatic nucleobases through parallel motif triplex formation
    摘要:
    2'-O,4'-C-methylene bridged nucleic acid (2',4'-BNA) monomers bearing novel unnatural nucleobases, 4-(3-benzamidophenyl)-2-pyridone and 2-(N-methylbenzamido)thiazole, were synthesized and successfully incorporated into oligonucleotides. UV melting experiments showed that the corresponding oligonucleotide derivatives formed stable triplexes with dsDNA targets even in the presence of a T center dot A interruption. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.043
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