3,5-Dinitrophenyl isocyanate

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Names

[ CAS No. ]:
59776-60-2

[ Name ]:
3,5-Dinitrophenyl isocyanate

[Synonym ]:
1-isocyanato-3,5-dinitrobenzene
MFCD00210046

Chemical & Physical Properties

[ Density]:
1.61g/cm3

[ Boiling Point ]:
338.6ºC at 760 mmHg

[ Melting Point ]:
82-87ºC(lit.)

[ Molecular Formula ]:
C7H3N3O5

[ Molecular Weight ]:
209.11600

[ Flash Point ]:
158.6ºC

[ Exact Mass ]:
209.00700

[ PSA ]:
121.07000

[ LogP ]:
2.51670

[ Index of Refraction ]:
1.654

[ Storage condition ]:
2-8℃

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07, GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H315-H317-H319-H334-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P342 + P311

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
36/37/38-42

[ Safety Phrases ]:
22-26-36

[ RIDADR ]:
UN3335 9

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • phosgene
  • 3,5-Dinitroaniline
  • Toluene
  • benzene
  • Acetone

DownStream

  • 3,5-Dinitroaniline
  • 1-[(1R,2R)-2-(dimethylamino)cyclohexyl]-3-(3,5-dinitrophenyl)urea

Articles

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 m...

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 composit...

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 ...


More Articles

Related Compounds

  • 3,5-dinitrophenyl phosphate
  • (3,5-dinitrophenyl)-(3,5-dinitrophenyl)imino-oxido-azanium
  • (3,5-dinitrophenyl)-(3-methyl-6-nitroindazol-1-yl)methanone
  • 3,5-Dinitrophenyl β-D-Galactoside
  • (3,5-dinitrophenyl) thiocyanate
  • (3,5-dinitrophenyl)-pyridin-1-ium-1-ylmethanone
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine