3,5-Dinitrophenyl isocyanate
3,5-Dinitrophenyl isocyanate structure
|
Common Name | 3,5-Dinitrophenyl isocyanate | ||
|---|---|---|---|---|
| CAS Number | 59776-60-2 | Molecular Weight | 209.11600 | |
| Density | 1.61g/cm3 | Boiling Point | 338.6ºC at 760 mmHg | |
| Molecular Formula | C7H3N3O5 | Melting Point | 82-87ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 158.6ºC | |
| Symbol |
GHS07, GHS08 |
Signal Word | Danger | |
|
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... |
|
|
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... |
|
|
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... |
|
|
High-performance liquid chromatographic separation of chiral alcohols on chiral stationary phases. Oi N and Kitahara H.
J. Chromatogr. A. 265 , 117-20, (1983)
|
|
|
Anthracene derivatives bearing two urea groups as fluorescent receptors for anions. Kim SK, et al.
Tetrahedron 61(19) , 4545-50, (2005)
|