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(14R,15R,114R,115R,4E,7E,14E,17E)-12,12,112,112-tetramethyl-3,4,8,9,13,14,18,19-octaaza-1,11(4,5)-didioxolana-6,16(1,4)-dibenzenacycloicosaphane-4,7,14,17-tetraene-2,10,12,20-tetraone | 1374018-89-9

中文名称
——
中文别名
——
英文名称
(14R,15R,114R,115R,4E,7E,14E,17E)-12,12,112,112-tetramethyl-3,4,8,9,13,14,18,19-octaaza-1,11(4,5)-didioxolana-6,16(1,4)-dibenzenacycloicosaphane-4,7,14,17-tetraene-2,10,12,20-tetraone
英文别名
——
(14R,15R,114R,115R,4E,7E,14E,17E)-12,12,112,112-tetramethyl-3,4,8,9,13,14,18,19-octaaza-1,11(4,5)-didioxolana-6,16(1,4)-dibenzenacycloicosaphane-4,7,14,17-tetraene-2,10,12,20-tetraone化学式
CAS
1374018-89-9
化学式
C30H32N8O8
mdl
——
分子量
632.633
InChiKey
WTIMWRNRBGTVGZ-UUBWAUQQSA-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):
    0.24
  • 重原子数:
    46.0
  • 可旋转键数:
    0.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    202.76
  • 氢给体数:
    4.0
  • 氢受体数:
    12.0

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

反应信息

  • 作为产物:
    参考文献:
    名称:
    An expedient synthesis and conformational features of acylhydrazone macrocycles derived from tartaric acid: evidence of water and π aromatic hydrogen bond interactions
    摘要:
    Tartaric acid dihydrazides with acetal protected hydroxy groups react with terephthalaldehyde to preferentially form [2+2] bisacylhydrazone macrocycles. The structures of these macrocycles display all anti N-N and C=N bonds. Both trans- and cis-C(O)-NH bonds are present in the macrocycle thus allowing the formation of a rather compact macrocyclic structure. The structures of the acylhydrazone macrocycle are shown to be different in the crystal and in the isolated molecule due to the structure determining role of water included in the crystal lattice: in the former all of the O=C-C-H bonds are anti, while in the latter both syn- and anti-bonds are present. Both the non-planarity of the bisacylhydrazone molecules and their chiral interchromophoric interactions contribute to the rotatory power of the molecule. The low-temperature X-ray crystal structure of this compound provides direct evidence for hydrogen bonding between water and the aromatic pi-electrons in the solid state. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2012.02.010
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