3,8-DIAMINO-6-PHENYLPHENANTHRIDINE

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Names

[ CAS No. ]:
52009-64-0

[ Name ]:
3,8-DIAMINO-6-PHENYLPHENANTHRIDINE

[Synonym ]:
MFCD00075152
EINECS 257-602-3
6-phenyl-phenanthridine-3,8-diyldiamine
2,7-Diamino-3-phenylphenanthridin
3,8-Diamino-6-phenylphenanthridine
6-Phenylphenathridine-3,8-diamine
6-Phenyl-phenanthridin-3,8-diyldiamin

Chemical & Physical Properties

[ Density]:
1.292g/cm3

[ Boiling Point ]:
558ºC at 760mmHg

[ Melting Point ]:
196-198 °C(lit.)

[ Molecular Formula ]:
C19H15N3

[ Molecular Weight ]:
285.34300

[ Flash Point ]:
325.6ºC

[ Exact Mass ]:
285.12700

[ PSA ]:
64.93000

[ LogP ]:
5.38180

[ Index of Refraction ]:
1.785

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

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

[ Hazard Codes ]:
Xn,Xi

[ Risk Phrases ]:
22-36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 3,8-Dinitro-6-phenyl-phenanthridine
  • Biphenyl
  • 2-Nitrobiphenyl
  • 2-Aminodiphenyl

DownStream

  • compound 76-805
  • 3,8-DI-(ETHOXYCARBONYLAMINO)-6-PHENYLPHENANTHRIDINE

Articles

Aromatic polyamides of 3, 8-diamino-6-phenylphenanthridine and their molecular complexes with sulfonated polystyrene ionomers. Cimecioglu AL, et al.

Macromolecules 28(18) , 6343-6346, (1995)

On the electronic structure of ethidium. Luedtke NW, et al.

Chemistry 11(2) , 495-508, (2005)

Binding of cationic and neutral phenanthridine Intercalators to a DNA oligomer is controlled by dispersion energy: Quantum chemical calculations and molecular mechanics simulations. Kubar T, et al.

Chemistry 12(1) , 280-290, (2006)


More Articles

Related Compounds

  • 3,8-DIAMINO-6-PHENYLPHENANTHRIDINE
  • carboxydimidium
  • 3-(3,8-diamino-6-phenylphenanthridin-5-ium-5-yl)propyl-diethyl-methylazanium,dibromide
  • 2-aminoethyl-p-carboxamide-methidium chloride
  • 4-(8-amino-5-ethyl-3-iminophenanthridin-6-yl)benzoic acid
  • 3,8-Diamino-5-ethyl-6-methylphenanthridinium bromide
  • 3-[4-(4-Chlorobenzyl)piperazin-1-yl]propanoic acid
  • N-cyclopropyl-2-(o-tolyl)-4-tosyloxazol-5-amine
  • 1-(4-((4-Fluorophenyl)sulfonyl)-2-(p-tolyl)oxazol-5-yl)piperidine-4-carboxamide
  • 1-(2-(o-Tolyl)-4-tosyloxazol-5-yl)piperidine-4-carboxamide
  • 2-amino-N-(4-ethylphenyl)-3-(4-methoxybenzoyl)indolizine-1-carboxamide
  • 2-(2-Furyl)-5-[(methylpropyl)amino]-4-(phenylsulfonyl)-1,3-oxazole
  • 1-(3-Hydroxypyrrolidin-1-yl)pentan-1-one
  • 5-(4-Ethylpiperazin-1-yl)-2-(furan-2-yl)-4-tosyloxazole
  • N-(4-fluorobenzyl)-2-(furan-2-yl)-4-[(4-methylphenyl)sulfonyl]-1,3-oxazol-5-amine
  • (3-Hydroxypyrrolidin-1-yl)(pyridin-2-yl)methanone
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