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

1-(2'-deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyrimidinone | 68780-64-3

中文名称
——
中文别名
——
英文名称
1-(2'-deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyrimidinone
英文别名
1-α-D-deoxyribofuranosyl-1,2-dihydropyrimidin-2-one;1-(2'-Desoxy-α-D-ribofuranosyl)-2(1H)-pyrimidinon;α-dZeb;1-(α-D-erythro-2-deoxy-pentofuranosyl)-1H-pyrimidin-2-one;1-(2'-Deoxyribosyl)-2-pyrimidinone;1-[(2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
1-(2'-deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyrimidinone化学式
CAS
68780-64-3
化学式
C9H12N2O4
mdl
——
分子量
212.205
InChiKey
QEJOIGZDWKFVCO-RNJXMRFFSA-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

  • 熔点:
    159 °C
  • 沸点:
    450.2±55.0 °C(Predicted)
  • 密度:
    1.57±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    82.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Polynucleotide assay reagent and method
    申请人:ANTIVIRALS INC.
    公开号:EP0639582A2
    公开(公告)日:1995-02-22
    The invention provides a use of a morpholino subunit of the formula (I) where P is a purine or pyrimidine base-pairing moiety, and T is H or an N-protective group, for the production of a polymer capable of hydrogen-bonding to complementary bases in a polynucleotide, where in said polymer (i) the subunits are joined predominantly by substantially uncharged, achiral linkages, and (ii) each linkage joins the morpholino nitrogen of one subunit to the 5' exocyclic carbon of an adjacent subunit.
    本发明提供了式 (I) 吗啉亚基的用途 其中 P 是嘌呤或嘧啶碱基配对分子,T 是 H 或 N 保护基团,用于生产能够与多核苷酸中的互补碱基发生氢键连接的聚合物,在所述聚合物中,(i) 亚基主要通过基本上不带电的非手性连接物连接,(ii) 每个连接物将一个亚基的吗啉基氮连接到相邻亚基的 5'外环碳上。
  • Efficient synthesis of 2′-deoxyzebularine and its α-anomer by the silyl method of N-glycosylation. Crystal structures and conformational study in solution
    作者:Katarzyna Ebenryter-Olbinska、Janina Karolak-Wojciechowska、Elzbieta Sochacka
    DOI:10.1016/j.carres.2014.03.018
    日期:2014.6
    2'-Deoxyzebularine and its alpha-anomer have been efficiently synthesized with relatively high stereoselectivity by a modified procedure of the silyl method of the N-glycosidic bond formation. An SnCl4-catalyzed condensation of silylated pyrimidin-2-one with 1-alpha-chloro-3,5-di-O-p-toluoy1-2-deoxy-D-ribofuranose under kinetic control condition (-33 degrees C, 1,2-dichloroethane) led to the mixture of beta- and alpha-anomeric nucleosides in 3:1 ratio. Analogous condensation at +35 degrees C (thermodynamic control conditions) provided mainly p-toluoyl protected alpha-2'-deoxyzebularine (alpha:beta= 4:1), easily separated by crystallization from the anomeric mixture. The structures of both 2'-deoxyzebularine anomers were confirmed by X-ray analysis of the crystals and conformational studies in solution performed using an NMR method. (C) 2014 Elsevier Ltd. All rights reserved.
  • SEELA, FRANK;BINDIG, UWE, LIEBIGS ANN. CHEM.,(1989) N, C. 895-901
    作者:SEELA, FRANK、BINDIG, UWE
    DOI:——
    日期:——
  • EP0215942A4
    申请人:——
    公开号:EP0215942A4
    公开(公告)日:1988-08-23
  • STEREOREGULAR POLYNUCLEOTIDE-BINDING POLYMERS
    申请人:SUMMERTON, James
    公开号:EP0216860A1
    公开(公告)日:1987-04-08
查看更多