N,N-二[2-(p-甲苯磺氧基)乙基]-p-甲苯磺酰胺
![N,N-二[2-(p-甲苯磺氧基)乙基]-p-甲苯磺酰胺结构式](https://image.chemsrc.com/caspic/487/16695-22-0.png)
N,N-二[2-(p-甲苯磺氧基)乙基]-p-甲苯磺酰胺结构式
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常用名 | N,N-二[2-(p-甲苯磺氧基)乙基]-p-甲苯磺酰胺 | 英文名 | Benzenesulfonamide,4-methyl-N,N-bis[2-[[(4-methylphenyl)sulfonyl]oxy]ethyl]- |
|---|---|---|---|---|
| CAS号 | 16695-22-0 | 分子量 | 567.69500 | |
| 密度 | 1.345g/cm3 | 沸点 | 732.4ºC at 760mmHg | |
| 分子式 | C25H29NO8S3 | 熔点 | 92-98ºC(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 396.8ºC | |
| 符号 |
GHS07 |
信号词 | Warning |
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Synthesis of 2-(p-thiocyanatobenzyl)-1,4,7-triazacyclononane-1,4,7-triacetic acid: application of the 4-methoxy-2,3,6-trimethylbenzenesulfonamide protecting group in the synthesis of macrocyclic polyamines.
Bioconjug. Chem. 4(3) , 236-45, (1993) A synthesis of the bifunctional chelator 2-(p-thiocyanatobenzyl)-1,4,7-triazacyclononane-1,4,7-triacetic acid [2-(p-NCS-Bz)-NOTA] is described which illustrates the especial utility of the (4-methoxy-2,3,6-trimethylphenyl)sulfonyl (Mtr) protecting group as an... |
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J. Org. Chem. 56 , 4904, (1991)
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Inorg. Chem. 31 , 3558, (1992)
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Rec. Trav. Chim. 110 , 124, (1991)
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