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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:
233-34-1
Molecular Weight:
167.21
NACRES:
NA.22
PubChem Substance ID:
24885828
UNSPSC Code:
12352100
MDL number:
MFCD02668148
Assay:
97%
Form:
solid
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Quality Level

100

assay

97%

form

solid

mp

180-184 °C

SMILES string

c1ccc2c(c1)ccc3cc[nH]c23

InChI

1S/C12H9N/c1-2-4-11-9(3-1)5-6-10-7-8-13-12(10)11/h1-8,13H

InChI key

HIYWOHBEPVGIQN-UHFFFAOYSA-N

Application

  • Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
Useful fused indole as a starter in indole chemistry.

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

hcodes

H301,H318

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCB0846V
02715CH

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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

Global Trade Item Number

SKUGTIN
684910-1G04061832758787