AE17071
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $62.00 | $44.00 | - + | |
5g | 96% | in stock | $240.00 | $168.00 | - + | |
25g | 97% | in stock | $763.00 | $534.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE17071 |
Chemical Name: | 1-Benzyl-5-bromoindole |
CAS Number: | 10075-51-1 |
Molecular Formula: | C15H12BrN |
Molecular Weight: | 286.1665 |
MDL Number: | MFCD04337704 |
SMILES: | Brc1ccc2c(c1)ccn2Cc1ccccc1 |
NSC Number: | 143237 |
Complexity: | 249 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Rotatable Bond Count: | 2 |
XLogP3: | 4.3 |
1-Benzyl-5-bromo-1H-indole is a versatile compound widely utilized in chemical synthesis for its unique properties. In organic chemistry, this compound serves as a valuable building block for the synthesis of various biologically active molecules and pharmaceuticals. Due to its bromine and benzyl functionalities, 1-Benzyl-5-bromo-1H-indole can undergo diverse chemical reactions, such as nucleophilic substitution, palladium-catalyzed coupling reactions, and Friedel-Crafts acylation. These reactions allow for the introduction of different functional groups, facilitating the synthesis of complex organic compounds.Moreover, the indole ring present in 1-Benzyl-5-bromo-1H-indole imparts aromatic character and provides opportunities for further diversification through electrophilic aromatic substitution reactions. This structural feature is particularly valuable in the construction of heterocyclic compounds and natural product synthesis.Overall, the strategic incorporation of 1-Benzyl-5-bromo-1H-indole in chemical synthesis enables chemists to access a wide range of structurally diverse molecules with potential applications in medicinal chemistry, material science, and agrochemical research.