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684910

Sigma-Aldrich

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
MDL number:
MFCD02668148
UNSPSC Code:
12352100
PubChem Substance ID:
24885828
NACRES:
NA.22

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

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.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H318

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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