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((2R,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-tetradecylamino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester | 294664-73-6

中文名称
——
中文别名
——
英文名称
((2R,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-tetradecylamino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester
英文别名
——
((2R,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-tetradecylamino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester化学式
CAS
294664-73-6
化学式
C25H50N2O6
mdl
——
分子量
474.682
InChiKey
SMQJLLPRUOTMOS-GNJRFXKQSA-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):
    3.61
  • 重原子数:
    33.0
  • 可旋转键数:
    16.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    120.28
  • 氢给体数:
    5.0
  • 氢受体数:
    7.0

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
  • 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:
    ((2R,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-tetradecylamino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester三氟乙酸 作用下, 以 四氢呋喃二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 37.0h, 生成 (Z)-N-(2-L-alanylamino-2-deoxy-β-D-glucopyranosyl)-N-tetradecyl-9-octadecenamide
    参考文献:
    名称:
    Syntheses of Peptidoglycolipid Analogs with Distinct Immunomodulating Activities
    摘要:
    Amphiphilic 2-amino-2-deoxy-beta-D-glucopyranosylamides were synthesized from N-protected glucosamine derivatives via N-glycosidation with fatty amines, subsequent N-acylation with fatty acid derivatives and deprotection. They could further be modified with amino acids to give peptido-glycopyranosyl amides, some of which exhibited strong immunostimulatory (BAY Q8939, 8) or immunoadjuvant (BAY R1005, 9) activities.
    DOI:
    10.1080/07328300008544102
  • 作为产物:
    参考文献:
    名称:
    Syntheses of Peptidoglycolipid Analogs with Distinct Immunomodulating Activities
    摘要:
    Amphiphilic 2-amino-2-deoxy-beta-D-glucopyranosylamides were synthesized from N-protected glucosamine derivatives via N-glycosidation with fatty amines, subsequent N-acylation with fatty acid derivatives and deprotection. They could further be modified with amino acids to give peptido-glycopyranosyl amides, some of which exhibited strong immunostimulatory (BAY Q8939, 8) or immunoadjuvant (BAY R1005, 9) activities.
    DOI:
    10.1080/07328300008544102
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