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AA33035

119793-66-7 | Propionyl-L-carnitine, HCl

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.

Description
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

 

Computed Properties
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  

 

 

Upstream Synthesis Route
  • 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.
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