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Ethyl 2-[40,41-bis(2-ethoxy-2-oxoethoxy)-5,13-dioxo-3,15-dioxa-6,9,12-triazahexacyclo[15.15.7.123,27.134,38.02,29.016,21]hentetraconta-1(32),2(29),16(21),17,19,23,25,27(41),30,34(40),35,37-dodecaen-9-yl]acetate | 250786-17-5

中文名称
——
中文别名
——
英文名称
Ethyl 2-[40,41-bis(2-ethoxy-2-oxoethoxy)-5,13-dioxo-3,15-dioxa-6,9,12-triazahexacyclo[15.15.7.123,27.134,38.02,29.016,21]hentetraconta-1(32),2(29),16(21),17,19,23,25,27(41),30,34(40),35,37-dodecaen-9-yl]acetate
英文别名
——
Ethyl 2-[40,41-bis(2-ethoxy-2-oxoethoxy)-5,13-dioxo-3,15-dioxa-6,9,12-triazahexacyclo[15.15.7.123,27.134,38.02,29.016,21]hentetraconta-1(32),2(29),16(21),17,19,23,25,27(41),30,34(40),35,37-dodecaen-9-yl]acetate化学式
CAS
250786-17-5
化学式
C48H55N3O12
mdl
——
分子量
865.978
InChiKey
UQSSSVQTIPYZOV-UHFFFAOYSA-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):
    6.9
  • 重原子数:
    63
  • 可旋转键数:
    14
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    177
  • 氢给体数:
    2
  • 氢受体数:
    13

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:
    Ethyl 2-[40,41-bis(2-ethoxy-2-oxoethoxy)-5,13-dioxo-3,15-dioxa-6,9,12-triazahexacyclo[15.15.7.123,27.134,38.02,29.016,21]hentetraconta-1(32),2(29),16(21),17,19,23,25,27(41),30,34(40),35,37-dodecaen-9-yl]acetatepotassium carbonate 作用下, 以 甲醇甲苯 为溶剂, 生成 Ethyl 2-(5,13,31,36-tetraoxo-3,15,29,38-tetraoxa-6,9,12,32,35-pentazaheptacyclo[25.22.1.117,40.02,46.016,21.023,28.039,44]henpentaconta-1(49),2(46),16,18,20,23,25,27,39(44),40,42,47-dodecaen-9-yl)acetate
    参考文献:
    名称:
    Studies on Calix(aza)crqwns, III. Synthesis of 1,3-Alternate Calix[4]arenes Capped by Diamide Bridges
    摘要:
    The alkylation of calix[4]arenes 1 capped by diamide bridges gave fully substituted compounds 5 and 6 of 1,3-alternate conformation. Diesters 6 were cyclized with diamines to afford doubly capped derivatives 7.
    DOI:
    10.1080/00397919908085912
  • 作为产物:
    描述:
    溴乙酸乙酯calix[4]amidocrown-5, conecaesium carbonate 作用下, 以 丙酮 为溶剂, 反应 4.0h, 以60%的产率得到Ethyl 2-[40,41-bis(2-ethoxy-2-oxoethoxy)-5,13-dioxo-3,15-dioxa-6,9,12-triazahexacyclo[15.15.7.123,27.134,38.02,29.016,21]hentetraconta-1(32),2(29),16(21),17,19,23,25,27(41),30,34(40),35,37-dodecaen-9-yl]acetate
    参考文献:
    名称:
    Studies on Calix(aza)crqwns, III. Synthesis of 1,3-Alternate Calix[4]arenes Capped by Diamide Bridges
    摘要:
    The alkylation of calix[4]arenes 1 capped by diamide bridges gave fully substituted compounds 5 and 6 of 1,3-alternate conformation. Diesters 6 were cyclized with diamines to afford doubly capped derivatives 7.
    DOI:
    10.1080/00397919908085912
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文献信息

  • Studies on Calix(aza)crqwns, III. Synthesis of 1,3-Alternate Calix[4]arenes Capped by Diamide Bridges
    作者:István Bitter、Alajos Grün、Barbara Balázs、Gábor Tóth、Gyula Horváth、László Töke
    DOI:10.1080/00397919908085912
    日期:1999.11
    The alkylation of calix[4]arenes 1 capped by diamide bridges gave fully substituted compounds 5 and 6 of 1,3-alternate conformation. Diesters 6 were cyclized with diamines to afford doubly capped derivatives 7.
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