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-Isocyanato-4,6-dimethylpyridine
  • 6-[(5-Methyl-1,2-oxazol-4-yl)methoxy]-1,2,3,4-tetrahydroisoquinoline
  • tert-butyl 3-(5-{[(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)oxy]carbonyl}-1-methyl-1H-pyrrol-2-yl)morpholine-4-carboxylate
  • 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 1-(1,3-oxazol-5-yl)bicyclo[2.1.1]hexane-5-carboxylate
  • rac-1-tert-butyl 2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl) (2R,3R)-3-phenylazetidine-1,2-dicarboxylate
  • 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl (2S,3aS,7aS)-1-(pyrimidin-2-yl)-octahydro-1H-indole-2-carboxylate
  • 1-tert-butyl 3'a-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl) 5'-(9H-fluoren-9-yl)methyl hexahydrospiro[azetidine-3,1'-furo[3,4-c]pyrrole]-1,3'a,5'-tricarboxylate
  • (9H-fluoren-9-yl)methyl 3-(4-{[(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)oxy]carbonyl}phenyl)-3-fluoroazetidine-1-carboxylate
  • 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 1-(4-fluorophenyl)-3-methyl-1H-pyrazole-4-carboxylate
  • 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-(5-methyl-1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoate
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