AB61290
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $9.00 | $7.00 | - + | |
1g | 97% | in stock | $15.00 | $11.00 | - + | |
5g | 97% | in stock | $50.00 | $35.00 | - + | |
10g | 97% | in stock | $97.00 | $68.00 | - + | |
25g | 97% | in stock | $194.00 | $136.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB61290 |
Chemical Name: | 2-(2-Bromoacetyl)thiophene |
CAS Number: | 10531-41-6 |
Molecular Formula: | C6H5BrOS |
Molecular Weight: | 205.0723 |
MDL Number: | MFCD02677721 |
SMILES: | BrCC(=O)c1cccs1 |
Complexity: | 116 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 2 |
XLogP3: | 2 |
The application of Ethanone, 2-bromo-1-(2-thienyl)- in chemical synthesis lies in its versatility as a key building block for the creation of various organic compounds. Due to its unique chemical structure, this compound serves as a fundamental intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science. The presence of the bromo and thienyl groups enables selective functionalization and molecular modifications, allowing for the formation of complex molecular structures. In organic chemistry, Ethanone, 2-bromo-1-(2-thienyl)- is commonly utilized in the construction of heterocyclic compounds and can participate in a range of reactions such as nucleophilic substitution, palladium-catalyzed coupling reactions, and cross-coupling reactions. Its strategic placement of functional groups makes it a valuable tool for customizing molecular structures with specific properties and functionalities, making it a cornerstone in modern synthetic chemistry.
Acta crystallographica. Section E, Structure reports online 20110301