684910
1H-Benzo[g]indole
97%
Synonym(s):
1H-Benz[g]indole, 6,7-Benzindole, NSC 153687
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About This Item
Empirical Formula (Hill Notation):
C12H9N
CAS Number:
Molecular Weight:
167.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Product Name
1H-Benzo[g]indole, 97%
InChI
1S/C12H9N/c1-2-4-11-9(3-1)5-6-10-7-8-13-12(10)11/h1-8,13H
SMILES string
c1ccc2c(c1)ccc3cc[nH]c23
InChI key
HIYWOHBEPVGIQN-UHFFFAOYSA-N
assay
97%
form
solid
mp
180-184 °C
Quality Level
Related Categories
Application
- Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
Useful fused indole as a starter in indole chemistry.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Jason Siu et al.
Organic & biomolecular chemistry, 2(2), 160-167 (2004-01-23)
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 of heteroaromatic enamine intermediates in good yield and high purities. Subsequent catalytic hydrogenation reactions
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