logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 5-Azaindole

AB68815

271-34-1 | 5-Azaindole

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.

Description
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

 

Computed Properties
Complexity: 103  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
XLogP3: 1  

 

 

Upstream Synthesis Route
  • 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.
FEATURED PRODUCTS