3,5-二异氰酸硝基苯
3,5-二异氰酸硝基苯结构式
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常用名 | 3,5-二异氰酸硝基苯 | 英文名 | 3,5-Dinitrophenyl isocyanate |
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| CAS号 | 59776-60-2 | 分子量 | 209.11600 | |
| 密度 | 1.61g/cm3 | 沸点 | 338.6ºC at 760 mmHg | |
| 分子式 | C7H3N3O5 | 熔点 | 82-87ºC(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 158.6ºC | |
| 符号 |
GHS07, GHS08 |
信号词 | Danger |
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New chiral high-performance liquid chromatographic methodology used for the pharmacokinetic evaluation of dexfenfluramine.
J. Chromatogr. B, Biomed. Appl. 654(2) , 231-48, (1994) A new chiral high-performance liquid chromatographic (HPLC) method utilizing ultraviolet (UV) detection has been developed for determining plasma and urinary concentrations of d-fenfluramine and its major metabolite d-norfenfluramine, while being able to dete... |
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Immobilized isocyanates for derivatization of amines for chiral recognition in liquid chromatography with UV detection.
J. Pharm. Biomed. Anal. 11(6) , 495-503, (1993) Solid-phase derivatization reagents containing a 3,5-dinitrophenyl moiety for the derivatization of amines are described. The reagents are useful for Pirkle-type recognition of stereochemical composition of amines and related nucleophiles. The ability to stab... |
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Enantiomeric analysis of phenylpropanolamine in plasma via resolution of dinitrophenylurea derivatives on a high performance liquid chromatographic chiral stationary phase.
Biomed. Chromatogr. 5(1) , 43-6, (1991) Racemic phenylpropanolamine was resolved on a high performance liquid chromatographic (HPLC) chiral stationary phase (CSP) as the 3,5-dinitrophenyl ureide derivative. The CSP was prepared by a simple in situ procedure in which (R)-(1-naphthyl)ethyl isocyanate... |
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High-performance liquid chromatographic separation of chiral alcohols on chiral stationary phases. Oi N and Kitahara H.
J. Chromatogr. A. 265 , 117-20, (1983)
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Anthracene derivatives bearing two urea groups as fluorescent receptors for anions. Kim SK, et al.
Tetrahedron 61(19) , 4545-50, (2005)
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