CAS: 69271-98-3; Bis((2,3,5,6,8,9,11,12-Octahydrobenzo[b][1,4,7,10,13]Pentaoxacyclopentadecin-15-yl)Methyl) Heptanedioate

该化合物是一种冠醚衍生物,由两个Benzo-15-crown-5组成,相互连接,增强了碱性和碱性土金属离子的复合性,其僵硬结构以及钾(K+)和钠(Na+)离子的高选择性使其在离子选择性电极,相继转移催化和分离过程中具有价值.该化合物的双冠醚糖在宿主座化学应用中提高了结合性和稳定性.其合成多功能性可以进一步功能化,使超分子化学和感应器的开发能够有针对性地使用.Bis(benzo-15-crown)在涉及离子运输和分子识别的研究中特别有用,因为其可预测的协调行为和在非水媒体中的强有力性能.

英文名称Bis((2,3,5,6,8,9,11,12-Octahydrobenzo[b][1,4,7,10,13]Pentaoxacyclopentadecin-15-yl)Methyl) Heptanedioate
中文名称钾离子载体 II
IUPAC名称bis((2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecin-15-yl)methyl) heptanedioate
其它别名Bis(2,5,8,11,14-Pentaoxabicyclo[13.4.0]Nonadeca-1(15),16,18-Trien-17-Ylmethyl) Heptanedioate; Bis[(Benzo-15-Crown-5)-15-Ylmethyl] Pimelate; Bis((2,3,5,6,8,9,11,12-Octahydrobenzo[b][1,4,7,10,13]Pen
CAS编号69271-98-3
MFCD编号:MFCD00012089
EINECS号:634-736-4
分子式:C37H52O14分子量:720.81
产品CID: 1688060
产品分类分析化学 → 分析试剂 → 常用分析试剂

相似结构搜索
InChIKey: LTZRCLYZVSXCTC-UHFFFAOYSA-N
InChI=1S/C37H52O14/c38-36(50-28-30-6-8-32-34(26-30)48-24-20-44-16-12-40-10-14-42-18-22-46-32)4-2-1-3-5-37(39)51-29-31-7-9-33-35(27-31)49-25-21-45-17-13-41-11-15-43-19-23-
计算化学: 氢键受体数14.0氢键供体数0.0可旋转键数12.0

MSDS等安全信息

GHS象形图
GHS符号GHS07;
注释: Exclamation mark
危险类别急性毒性类别4(吸入)
急性毒性类别4(经皮)
急性毒性类别4(经口)
特定目标器官毒性 - 单次接触类别3
皮肤腐蚀/刺激类别2
严重眼刺激类别2
警示词Warning(警告)
危险描述H332 |吸入有害.
H312 |皮肤接触有害.
H302 |吞咽有害.
H335 |可能引起呼吸道刺激.
H315 |造成皮肤刺激.
H319 |造成严重眼刺激.
防范说明P261-P280-P301+P312-P302+P352+P312-P304+P340+P312-P305+P351+P338
UN编号NONH for all modes of transport
危险品标志Xn
安全声明26-36
危险类别码20/21/22-36/37/38
WGK Germany3

欧盟法规

ECHA物质C&L通报

合成工艺路线路线简述

海关参考信息

2902300000-甲苯
2905121000-正丙醇
2905130000-正丁醇
2905310000-1,2-乙二醇
💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
详情请参考：📖 海关编码查询和海关进出口税则

专利信息

专利号:US-9550704-B2
优先权日:2012-05-24
标题 :Method for synthesizing radiopharmaceuticals using a cartridge
发明人：CHI DAE YOON; LEE BYOUNG SE; LEE JAE HAK; CHU SO YOUNG; JUNG WOON JUNG
权利人:FUTURECHEM CO LTD
摘要:The present invention relates to a method for synthesizing a radiopharmaceutical using a cartridge, which makes it possible to carry out several steps of reaction required for synthesizing a radiopharmaceutical in the cartridge filled with a polymer. A method for synthesizing a radiopharmaceutical according to the present invention enables each step's reaction to be carried out with the solution confined in the cartridge so as not to flow out, thus being simplified compared to the conventional methods for synthesizing radiopharmaceuticals, and expediting the synthesis thereof.