1H-Benz[g]indole

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

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

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...

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
4-(Isopropylsulfonyl)benzonitrile
4-(2-Methylpropane-1-sulfonyl)-benzonitrile
N-(3-phenylpropyl)cyclobutanamine
3-Methoxy-6-methylpyrazine-2-carboxylic acid
1-Benzyl-5-(chloromethyl)pyrrolidin-2-one
Diethyl [(4-aminophenyl)(hydroxy)methyl]-phosphonate
tert-butyl N-methyl-N-[2-(methylsulfanyl)ethyl]carbamate
methyl 3-[2-(1H-benzoimidazol-1-yl)-4-(3-chlorophenyl)-5-oxazolyl]propionate
Methyl [2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)-5-oxazolyl]carboxylate
Tert-butyl 2-(ethylsulfonyl)ethylcarbamate

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