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55528-53-5

H-LYS(ME)3-OH CHLORIDE

Catalog#: AR00DJVU  |   CAS#: 55528-53-5  |   MDL#: MFCD06795777  |   MF: C9H21ClN2O2  |   MW: 224.7282

Packsize Purity Price Availability Quantity
5mg 98% $115.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DJVU
Chemical Name H-LYS(ME)3-OH CHLORIDE
CAS Number 55528-53-5
Molecular Formula C9H21ClN2O2
Molecular Weight 224.7282
MDL Number MFCD06795777
SMILES OC(=O)[C@H](CCCC[N+](C)(C)C)N.[Cl-]

(S)-5-Amino-5-carboxy-N,N,N-trimethylpentan-1-aminium chloride is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable chiral building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its asymmetric center allows for the creation of enantiomerically pure products, making it a valuable tool in the production of optically active compounds.One of the key applications of (S)-5-Amino-5-carboxy-N,N,N-trimethylpentan-1-aminium chloride is in asymmetric synthesis, where it acts as a chiral auxiliary or a chiral ligand in catalytic processes. By incorporating this compound into a reaction, chemists can efficiently control the stereochemistry of the products, leading to higher yields of desired enantiomers. This compound is particularly useful in the synthesis of amino acids, peptides, and complex natural products where stereochemistry plays a crucial role in determining biological activity.Additionally, (S)-5-Amino-5-carboxy-N,N,N-trimethylpentan-1-aminium chloride can be utilized in the preparation of chiral catalysts for asymmetric transformations, such as asymmetric hydrogenation, asymmetric allylation, and asymmetric Michael additions. Its unique structure and reactivity allow for the development of efficient and selective catalytic processes, enabling chemists to access a wide range of chiral compounds with high enantioselectivity.Overall, (S)-5-Amino-5-carboxy-N,N,N-trimethylpentan-1-aminium chloride is a valuable tool in chemical synthesis, offering chemists a versatile and efficient way to introduce chirality into their target molecules. Its applications in asymmetric synthesis and catalysis make it an essential component in the toolbox of synthetic chemists aiming to access enantiomerically pure compounds for various applications.
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