| Bioactivity | 1H-Indol-5-amine (5-Aminoindole) can be utilized as absorbent for hydrophobic charge induction chromatography (HCIC), or synthesis of tetracyclic heterocycles through the three-component reaction[1][2]. |
| CAS | 5192-03-0 |
| Formula | C8H8N2 |
| Molar Mass | 132.16 |
| Appearance | 固体 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | 4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
| Reference | [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. [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. |
1H-Indol-5-amine
CAS: 5192-03-0 F: C8H8N2 W: 132.16
1H-Indol-5-amine (5-Aminoindole) can be utilized as absorbent for hydrophobic charge induction chromatography (HCIC), or
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