1H-Indol-5-amine
Based on 1 Customer Validation
1H-Indol-5-amine (5-Aminoindole) is an organic compound containing an indole ring structure and belongs to the class of indole derivatives. 1H-Indol-5-amine can serve as a key intermediate for the synthesis of other active compounds.
For research use only. We do not sell to patients.
- Purity: 98.0%
- CAS No.: 5192-03-0
- Formula: C8H8N2
- Molecular Weight:132.17
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Storage:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
- Purity & Documentation
- References
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Help & FAQs
Biological Activity
1H-Indol-5-amine undergoes a three-component reaction with aromatic aldehydes and tert-butyl 2,4-dioxopiperidine-1-carboxylate under catalyst-free conditions by refluxing in ethanol, yielding 11-aryl-3H-indolo[5,4-b][1,6]naphthyridine derivatives[1].
1H-Indol-5-amine is a ligand used for preparing AI-Sepharose hydrophobic charge induction chromatography medium, which can achieve protein adsorption and elution through hydrophobic interaction and pH-induced charge repulsion, and has application potential in protein purification[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 5192-03-0
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Appearance Solid
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Molecular Weight 132.17
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Formula C8H8N2
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Color Light brown to black
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SMILES
NC1=CC2=C(NC=C2)C=C1
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Synonyms
5-Aminoindole
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Purity & Documentation
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Data Sheet (268 KB)
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SDS (624 KB)
- English - EN (624 KB)
- Français - FR (624 KB)
- Deutsch - DE (624 KB)
- Norwegian - NO (624 KB)
- Español - ES (624 KB)
- Swedish - SV (624 KB)
- Italian - IT (624 KB)
- Korean - KR (624 KB)
- Portuguese - PT (624 KB)
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Handling Instructions (2659 KB)
References
[1]. Li C, et al., Combinatorial synthesis of fused tetracyclic heterocycles containing [1,6]naphthyridine derivatives under catalyst free conditions. ACS Comb Sci. 2013 May 13;15(5):267-72. [Content Brief]
[2]. Zhao G, et al., 5-Aminoindole, a new ligand for hydrophobic charge induction chromatography. J Chromatogr A. 2008 Nov 21;1211(1-2):90-8. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
1H-Indol-5-amine Related Classifications
HY-W007509 Related Classifications
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