1H-Benz[g]indole

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Names

[ CAS No. ]:
233-34-1

[ Name ]:
1H-Benz[g]indole

[Synonym ]:
1h-benzo(g)indole

Chemical & Physical Properties

[ Density]:
1.229g/cm3

[ Boiling Point ]:
371.1ºC at 760mmHg

[ Melting Point ]:
180-184ºC

[ Molecular Formula ]:
C12H9N

[ Molecular Weight ]:
167.20700

[ Flash Point ]:
168.8ºC

[ Exact Mass ]:
167.07300

[ PSA ]:
15.79000

[ LogP ]:
3.32110

[ Vapour Pressure ]:
2.26E-05mmHg at 25°C

[ Index of Refraction ]:
1.767

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H318

[ Precautionary Statements ]:
P280-P301 + P310-P305 + P351 + P338

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

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
22-41

[ Safety Phrases ]:
26

[ RIDADR ]:
UN 2811 6.1/PG 3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2-(DIMETHYLAMINO)VINYL-1-NITRONAPHTHAL&
  • 1-Aminonaphthalene
  • Ethylene glycol
  • 4,5-dihydro-1H-benzo[g]indole
  • 1-Nitronaphthalene
  • Vinylmagnesium bromide
  • 2-Methyl-1-nitronaphthalene
  • 1-Amino-2-bromonaphthalene
  • ethyl (2-bromonaphthalen-1-yl)carbamate

DownStream

  • 1H-Benzo[g]indole-3-carboxaldehyde

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

Microwave assisted Leimgruber-Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines.

Org. Biomol. Chem. 2 , 160, (2004)

The development of enhanced conditions for Lewis acid catalysed Leimgruber-Batcho indole synthesis using microwave acceleration is described. This approach has permitted the preparation of a variety o...


More Articles

Related Compounds

  • 1H-Benz[g]indole-2,3-dione
  • 2,3-dimethyl-1H-benz[g]indole
  • 1H-Benz[g]indole,1,2,3-trimethyl
  • 6,7,8,9-tetrahydro-1H-benz[g]indole-2,3-dione
  • 1H-Benz[g]indole-2-carboxaldehyde,4,5-dihydro
  • ethyl 5-chloro-1H-benz[g]indole-2-carboxylate
  • (2-Cyano-2-{[3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-ylmethyl)-phenyl]-hydrazono}-acetyl)-carbamic acid ethyl ester
  • Tert-butyl 4-((4-chloroquinazolin-6-yl)oxy)piperidine-1-carboxylate
  • (6-Bromo-pyridin-3-yl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanol
  • 5-(3-fluoro-4-methylphenyl)-1H-imidazol-2-amine
  • (2-Chlorophenyl)(5-chloropyridin-2-yl)methanol
  • 5-(3-fluoro-4-methylphenyl)-1H-pyrazole-3-carboxylic acid
  • Methyl 3-(3-fluoro-4-methylphenyl)-3-methyloxirane-2-carboxylate
  • 3-(3-Fluoro-4-methylphenyl)butan-2-ol
  • 5-(4-Aminophenyl)nicotinonitrile
  • Methyl 4-[[(methylsulfonyl)oxy]methyl]cyclohexanecarboxylate
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