525022
4-Aminoindole
97%
Synonym(s):
(Indol-4-yl)amine, 4-Indolamine
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About This Item
Empirical Formula (Hill Notation):
C8H8N2
CAS Number:
Molecular Weight:
132.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
114919
Product Name
4-Aminoindole, 97%
InChI
1S/C8H8N2/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,9H2
SMILES string
Nc1cccc2[nH]ccc12
InChI key
LUNUNJFSHKSXGQ-UHFFFAOYSA-N
assay
97%
mp
106-109 °C (lit.)
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Application
4-Aminoindole may be used to synthesize:
- macrolactam tumour promoter indolactam V
- tricyclic structure of 2-substituted-pyrrolo[2,3-h]quinolin-4-one
- 4-azidoindole
Reactant for preparation of:
- Inhibitors of bacterial thymidylate synthase
- Mimetics of non-alkaloid toxin lignan anticancer and antiviral agent Podophyllotoxin (PPT)
- Inhibitors of Gli1-mediated transcription in the Hedgehog pathway
- Protein kinase C θ (PKCθ) inhibitors
- Indolic non-peptidic HIV protease inhibitors
- Transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonists
- Cyclooxygenase-2 (COX-2) and lipoxygenase (LOX) inhibitors
- 11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) inhibitors
- Short chain 4-substituted indoles as potent αvβ3 antagonist
- Ligands of serotonin transporter and 5-HT1A receptors
General description
4-Aminoindole is an indole derivative. Its cytokinin activity has been assessed by tobacco pith callus bioassay. 4-Aminoindole can be prepared by reacting 2,6-dinitrotoluene and N,N-dimethylformamide dimethylacetal in anhydrous DMF.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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An efficient synthesis of azidoindoles and azidotryptophans.
Melhado LL and Leonard NJ.
The Journal of Organic Chemistry, 48(25), 5130-5133 (1983)
Synthestic approaches to the teleocidin-related tumour promoters: a total synthesis of (?)-indolactam V.
de Laszlo SE, et al.
Journal of the Chemical Society. Chemical Communications, 4, 344-346 (1986)
Maria Grazia Ferlin et al.
Journal of medicinal chemistry, 48(9), 3417-3427 (2005-04-29)
In our search for potential new anticancer drugs, we designed and synthesized a series of tricyclic compounds containing the antimitotic 2-phenylazaflavone chromophore fused to a pyrrole ring in a pyrroloquinoline structure. Compounds 8, 18, 19, 22, 23, 25 and 26
Cytokinin activity of azaindene, azanaphthalene, naphthalene, and indole derivatives.
Torigoe Y, et al.
Phytochemistry, 11(5), 1623-1630 (1972)
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