2-phenylindole-3-carboxaldehyde

Suppliers

Names

[ CAS No. ]:
25365-71-3

[ Name ]:
2-phenylindole-3-carboxaldehyde

[Synonym ]:
MFCD00435481
2-Phenylindole-3-carbaldehyde
2-phenyl-3-formylindole
3-Formyl-2-phenylindole
2-phenyl-1H-indol-3-carboxaldehyde
2-Phenylindole-3-carboxaldehyde

Chemical & Physical Properties

[ Density]:
1.237 g/cm3

[ Boiling Point ]:
462.9ºC at 760 mmHg

[ Melting Point ]:
249-253 °C(lit.)

[ Molecular Formula ]:
C15H11NO

[ Molecular Weight ]:
221.25400

[ Flash Point ]:
237.5ºC

[ Exact Mass ]:
221.08400

[ PSA ]:
32.86000

[ LogP ]:
3.64740

[ Vapour Pressure ]:
9.47E-09mmHg at 25°C

[ Index of Refraction ]:
1.709

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

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

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Precursor & DownStream

Precursor

  • 2-Phenylindole
  • N,N-Dimethylformamide
  • 2-bromo-1H-indole-3-carbaldehyde
  • Tetraphenylstannane
  • N,N,N-trimethyl-1-(2-phenyl-1H-indol-3-yl)methanaminium iodide
  • TMEDA
  • 10-methoxy-6,10-dimethylundec-3-en-2-one
  • 2,2,2-trifluoro-N-[2-(2-phenylethynyl)phenyl]acetamide
  • Aminoform

DownStream

  • tert-butyl 3-formyl-2-phenylindole-1-carboxylate
  • 2-(Benzoylamino)benzoic acid
  • Methyl-2-phenyl -3-formylindole
  • 2-phenyl-1H-indole-3-carbonitrile
  • 3-formyl-2-phenyl-1H-indole-1-propiononitrile

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis of 2-arylindole derivatives and evaluation as nitric oxide synthase and NFκB inhibitors.

Org. Biomol. Chem. 10(44) , 8835-47, (2012)

Development of small molecule drug-like inhibitors blocking both nitric oxide synthase and NFκB could offer a synergistic therapeutic approach in the prevention and treatment of inflammation and cance...

Iridium-catalyzed regio- and enantioselective N-allylation of indoles.

Angew. Chem. Int. Ed. Engl. 48(42) , 7841-4, (2009)

Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines: facile synthesis of bisindolyl-and indolyl-heterocyclic alkanes. Kumar S, et al.

Tetrahedron Lett. 44(10) , 2101-2104, (2003)


More Articles


Related Compounds

  • 2-Phenylindole-3-carboxaldehyde
  • 5-chloro-2-phenylindole-3-carboxaldehyde
  • 5-methyl-2-phenylindole-3-carboxaldehyde
  • 1-Methyl-2-Phenylindole-3-Carboxaldehyde
  • 2-Phenylindole-3-carboxaldehyde,4-(o-methoxyphenyl)-3-thiosemicarbazone
  • 2-Phenylindole-3-carboxamide