1H-Indol-5-amine

CAT:

804-HY-W007509-02

Size:

10 g

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CAS Number: 5192-03-0
UNSPSC Description: 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].
Target Antigen: Biochemical Assay Reagents
Type: Biochemical Assay Reagents
Related Pathways: Others
Field of Research: Others
Assay Protocol: https://www.medchemexpress.com/1h-indol-5-amine.html
Purity: 98.0
Solubility: 10 mM in DMSO
Smiles: NC1=CC2=C(NC=C2)C=C1
Molecular Weight: 132.166
References & Citations: [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.
Shipping Conditions: Room Temperature
Storage Conditions: 4°C (Powder, protect from light)
Clinical Information: No Development Reported

Cat	Name
HY-W007509-01	1H-Indol-5-amine
HY-W007509-02	1H-Indol-5-amine
HY-W320032	5-Bromo-1H-indol-3-yl octanoate
HY-W041232-02	5-Phenyl-1H-pyrazol-3-amine
HY-W041232-01	5-Phenyl-1H-pyrazol-3-amine
HY-D0910-04	5-Bromo-6-chloro-1H-indol-3-yl acetate
HY-D0910-03	5-Bromo-6-chloro-1H-indol-3-yl acetate
HY-D0910-05	5-Bromo-6-chloro-1H-indol-3-yl acetate
HY-D0910-02	5-Bromo-6-chloro-1H-indol-3-yl acetate
HY-D0910-01	5-Bromo-6-chloro-1H-indol-3-yl acetate

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