AB70202
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 95% | in stock | $33.00 | $23.00 | - + | |
5g | 95% | in stock | $60.00 | $42.00 | - + | |
10g | 95% | in stock | $100.00 | $70.00 | - + | |
25g | 95% | in stock | $122.00 | $86.00 | - + | |
100g | 95% | in stock | $355.00 | $248.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB70202 |
Chemical Name: | 8-Amino-2-(2h-tetrazol-5-yl)-4h-chromen-4-one hydrochloride |
CAS Number: | 110683-23-3 |
Molecular Formula: | C10H8ClN5O2 |
Molecular Weight: | 265.6558 |
MDL Number: | MFCD09907720 |
SMILES: | Nc1cccc2c1oc(cc2=O)c1n[nH]nn1.Cl |
The 8-Amino-2-(2H-tetrazol-5-yl)-4H-chromen-4-one hydrochloride is a versatile compound widely used in chemical synthesis as a key building block for the development of novel pharmaceuticals, agrochemicals, and materials. This compound serves as a valuable intermediate in organic synthesis due to its unique structure and reactivity. In chemical reactions, it can act as a nucleophile, electrophile, or radical precursor, allowing for the formation of complex molecular structures.One significant application of 8-Amino-2-(2H-tetrazol-5-yl)-4H-chromen-4-one hydrochloride is in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. By utilizing this compound as a starting material, chemists can create diverse libraries of compounds with potential biological activities. Additionally, its tetrazole moiety can serve as a bioisostere for carboxylic acids, enhancing the pharmacokinetic properties of the resulting molecules.Furthermore, the hydrochloride salt form of 8-Amino-2-(2H-tetrazol-5-yl)-4H-chromen-4-one provides improved solubility and stability in aqueous environments, making it suitable for various synthetic transformations under mild conditions. Its presence in the synthesis of biologically active compounds underscores its importance in medicinal chemistry and chemical biology research.