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(3aS,4S,6R,6aS)-6-[(4R)-2,2-二甲基-1,3-二氧戊环-4-基]-N-羟基-2,2-二甲基四氢呋喃并[3,4-d][1,3]二氧杂环戊烯-4-胺 | 35023-80-4

中文名称
(3aS,4S,6R,6aS)-6-[(4R)-2,2-二甲基-1,3-二氧戊环-4-基]-N-羟基-2,2-二甲基四氢呋喃并[3,4-d][1,3]二氧杂环戊烯-4-胺
中文别名
二丙酮甘露糖肟
英文名称
(2,2-dimethyl-1,3-dioxolan-4-yl)-[5-[(Z)-hydroxyiminomethyl]-2,2-dimethyl-1,3-dioxolan-4-yl]methanol
英文别名
——
(3aS,4S,6R,6aS)-6-[(4R)-2,2-二甲基-1,3-二氧戊环-4-基]-N-羟基-2,2-二甲基四氢呋喃并[3,4-d][1,3]二氧杂环戊烯-4-胺化学式
CAS
35023-80-4;104012-85-3;104320-20-9;129312-24-9;129312-25-0;129312-26-1;129312-27-2;129312-29-4;129312-30-7
化学式
C12H21NO6
mdl
——
分子量
275.302
InChiKey
GCYSHDWLKNPSBV-ACAGNQJTSA-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):
    -0.1
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    89.7
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • METHOD FOR THE GENERATION OF CHEMICAL LIBRARIES
    申请人:ETH ZURICH
    公开号:US20170088878A1
    公开(公告)日:2017-03-30
    A method for the generation of oligomers or a mixture of oligomers to form a chemical library by amide-forming oligomerization comprises the steps of 1) reacting a mixture of at initiator (I) with monomer (M) to form a dimer of the initiator (I) and the monomer (M) or a pre-oligomer with an initiator (I) attached to a chain of more than one monomer (M) or a mixture thereof by amide-bond formation; 2) optionally adding at least one terminator (T) for the formation of a linear oligomer or a mixture of linear oligomers by amide-bond formation; or, for the formation of a cyclic oligomer or a mixture of cyclic oligomers by amide-bond formation, changing the reaction conditions relative to step 1) so as to form a linking covalent bond between the at least one initiator (I).
  • [EN] METHOD FOR THE GENERATION OF CHEMICAL LIBRARIES<br/>[FR] PROCÉDÉ DE GÉNÉRATION DE BANQUES CHIMIQUES
    申请人:ETH ZUERICH
    公开号:WO2015124443A1
    公开(公告)日:2015-08-27
    A method for the generation of oligomers or a mixture of oligomers to form a chemical library by amide-forming oligomerization comprises the steps of ) reacting a mixture of at least one initiator (I) with at least one monomer (M) to form a dimer of the initiator (I) and the monomer (M) or a pre-oligomer with an initiator (I) attached to a chain of more than one monomer (M) or a mixture thereof by amide-bond formation; 2) optionally adding at least one terminator (T) for the formation of a linear oligomer or a mixture of linear oligomers by amide-bond formation; or, for the formation of a cyclic oligomer or a mixture of cyclic oligomers by amide-bond formation, changing the reaction conditions relative to step 1) so as to form a linking covalent bond between the at least one initiator (I) and preferably the respective terminal monomer (M) of the dimer or pre-oligomer formed in step 1).
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