AA33035
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $16.00 | $11.00 | - + | |
5g | 95% | in stock | $26.00 | $18.00 | - + | |
25g | 95% | in stock | $73.00 | $52.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA33035 |
Chemical Name: | Propionyl-L-carnitine, HCl |
CAS Number: | 119793-66-7 |
Molecular Formula: | C10H20ClNO4 |
Molecular Weight: | 253.7231 |
MDL Number: | MFCD00274137 |
SMILES: | CCC(=O)O[C@@H](C[N+](C)(C)C)CC(=O)O.[Cl-] |
NSC Number: | 759826 |
Complexity: | 232 |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 7 |
The (2R)-3-carboxy-N,N,N-trimethyl-2-(1-oxopropoxy)-1-propanaminium chloride is a versatile chemical reagent commonly used in chemical synthesis. It serves as an efficient chiral quaternary ammonium salt that can be employed in various reactions due to its unique structural properties. Specifically, this compound is favored in asymmetric transformations and catalytic processes where chirality plays a crucial role in determining the stereochemistry of the final product.In chemical synthesis, (2R)-3-carboxy-N,N,N-trimethyl-2-(1-oxopropoxy)-1-propanaminium chloride functions as a valuable catalyst or chiral auxiliary. It can facilitate the formation of new carbon-carbon or carbon-heteroatom bonds with high enantioselectivity, leading to the production of optically pure compounds. Additionally, this compound can participate in key steps of complex organic reactions, enabling the selective formation of specific stereoisomers essential for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.Overall, the application of (2R)-3-carboxy-N,N,N-trimethyl-2-(1-oxopropoxy)-1-propanaminium chloride in chemical synthesis showcases its significance as a fundamental building block for achieving stereocontrol and enhancing the efficiency of asymmetric transformations in the synthesis of valuable organic molecules.