AB68815
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $8.00 | $5.00 | - + | |
1g | 98% | in stock | $9.00 | $6.00 | - + | |
5g | 98% | in stock | $20.00 | $14.00 | - + | |
10g | 98% | in stock | $36.00 | $25.00 | - + | |
25g | 98% | in stock | $75.00 | $52.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB68815 |
Chemical Name: | 5-Azaindole |
CAS Number: | 271-34-1 |
Molecular Formula: | C7H6N2 |
Molecular Weight: | 118.13594 |
MDL Number: | MFCD00955936 |
SMILES: | c1ncc2c(c1)[nH]cc2 |
Complexity: | 103 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 1 |
5-Azaindole, also known as 1-Azaindole or isogaupfromarine, is a heterocyclic compound with a five-membered ring structure containing both nitrogen and carbon atoms at positions 1 and 3, respectively. This unique molecular arrangement imparts valuable properties that make 5-Azaindole a versatile building block in chemical synthesis.One of the key applications of 5-Azaindole in chemical synthesis is its utility as a precursor in the preparation of various pharmaceuticals and agrochemicals. Due to its ability to efficiently participate in diverse chemical reactions, 5-Azaindole serves as a fundamental intermediate in the synthesis of biologically active compounds. Researchers and chemists often leverage the reactivity of 5-Azaindole to introduce specific functionalities or structural motifs into target molecules, thereby enabling the creation of new drug candidates or crop protection agents.Additionally, 5-Azaindole exhibits ligand properties, making it a valuable component in catalytic systems for organic transformations. Its nitrogen-containing heterocyclic nature enables coordination with transition metals, facilitating catalytic processes such as cross-coupling reactions, asymmetric synthesis, and metal-catalyzed transformations. By incorporating 5-Azaindole derivatives into catalytic systems, chemists can enhance reaction selectivity, efficiency, and overall yields in various synthetic protocols.In summary, the strategic placement of nitrogen and carbon atoms in the 5-Azaindole scaffold, coupled with its reactivity and diverse applications in chemical synthesis, positions this heterocyclic compound as a valuable tool for developing novel compounds with potential pharmaceutical and agrochemical applications.