摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-(4-nitrophenyl)-D-galactosylamine | 10399-84-5

中文名称
——
中文别名
——
英文名称
N-(4-nitrophenyl)-D-galactosylamine
英文别名
(2R,3R,4S,5R)-2-(hydroxymethyl)-6-(4-nitroanilino)oxane-3,4,5-triol
N-(4-nitrophenyl)-D-galactosylamine化学式
CAS
10399-84-5
化学式
C12H16N2O7
mdl
——
分子量
300.268
InChiKey
ONVNCZJMOXIVHT-SCWFEDMQSA-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):
    -0.4
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    148
  • 氢给体数:
    5
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    N-(4-nitrophenyl)-D-galactosylamine碘甲烷sodium hydroxide 作用下, 以 二甲基亚砜 为溶剂, 反应 0.25h, 以82%的产率得到N-methyl-N-(4-nitrophenyl)-2,3,4,6-tetra-O-methyl-β-D-galactopyranosylamine
    参考文献:
    名称:
    Selective defucosylation by mercaptolysis. A potential step in analyzing branched oligosaccharides
    摘要:
    A method of stepwise chemical degradation was elaborated on a mu g quantity of 3-O-alpha-L-fucosyllactose. The key step, TiCl4-catalysed dithioacetal formation from the permethylated N-4-nitrophenyl triosylamine (4) was accompanied by quantitative defucosylation. [C-14]Acetylation of the dried mercaptalation mixture gave radiolabelled 3,5-di-O-[C-14]acetyl-4-O-(2,3,4,6-tetra-O-methyl-beta-D-galactopyranosyl)-2,6-diO-methyl-D-glucose diethyl dithioacetal (7) and 5-O-[C-14]acetyl-2,3,4-tri-O-methyl-L-fucose diethyl dithioacetal (8). The former was further degraded via the bis(sulfone), and thereby 2,3,4,6-tetra-O-methyl-D-galactose (13) was expelled. The monosaccharide branches, fucose and galactose, were identified as derivatives 8 and 13, respectively, by comparison with authentic samples. Isolation of microquantities of products was carried out by preparative TLC.
    DOI:
    10.1016/s0008-6215(05)80006-0
点击查看最新优质反应信息