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CAS RN: 6066-82-6 | 产品编码: B0249
N-Hydroxysuccinimide [Coupling Reagent for Peptide]
![N-Hydroxysuccinimide [Coupling Reagent for Peptide] No-Image](/medias/B0249.jpg?context=bWFzdGVyfHJvb3R8NDU1OTh8aW1hZ2UvanBlZ3xhR1poTDJneE1pODRPVEU1TnpVek5Ea3dORFl5TDBJd01qUTVMbXB3Wnd8YmIzODhjODMwOWFlOGUyNmQwMWVlYmNlNGJmODFmNzgwOTI1YzYxY2I2YWE1YjJmY2YwZWViMTQwNmZiNjViZg)
技术规格
Appearance | White to Almost white powder to crystal |
Purity(GC) | min. 98.0 % |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 98.0 to 102.0 °C |
Solubility in Dioxane | lmost transparency |
NMR | confirm to structure |
物性(参考值)
熔点 | 100 °C |
水溶性 | 可溶 |
溶解性(可溶于) | 二噁烷 |
GHS
相关法规
运输信息
HS编码* | 2928.00-000 |
应用
An Additive for Condensation Reactions
Experimental procedure: A mixture of 1 (3.8 g, 17.5 mmol) and N-hydroxysuccinimide (3.0 g, 26.2 mmol) in CH2Cl2 (100 mL) and THF (50 mL) at 0 °C is treated with EDC・HCl (5.0 g, 26.2 mmol), and the mixture is stirred at the same temperature for 12 h. The reaction is quenched with H2O, and the mixture is partitioned between AcOEt and H2O. The organic phase is washed with saturated aqueous NaCl, dried (Na2SO4), filtered, and concentrated in vacuo. The residue (2) in CH2Cl2 (100 mL) is treated with 3-amino-1-propanol (2.0 mL, 26.2 mmol) at 0 °C and stirred at room temperature for 8 h. The resulting mixture is partitioned between AcOEt and H2O. The organic phase is washed with H2O (twice), saturated aqueous NaCl, dried (Na2SO4), filtered, and concentrated in vacuo. The residue is purified by silica gel column chromatography (40% AcOEt-hexane) to afford 3 as a colorless syrup (4.0 g, 84% over two steps).
References
- Mechanistic Analysis of Muraymycin Analogues: A Guide to the Design of MraY Inhibitors
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