CAS 1208162-98-4
:N-a-methyl-D-leucine benzyl ester p-tosylate
Description:
N-a-methyl-D-leucine benzyl ester p-tosylate is a chemical compound characterized by its structure, which includes a D-leucine derivative with a methyl group at the nitrogen position, a benzyl ester functional group, and a p-toluenesulfonate (p-tosylate) moiety. This compound is typically used in organic synthesis and peptide chemistry due to its ability to act as a protecting group for amino acids and its role in facilitating various coupling reactions. The presence of the p-tosylate group enhances the compound's solubility and reactivity, making it useful in nucleophilic substitution reactions. Additionally, the benzyl ester provides stability and can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Its stereochemistry, being derived from D-leucine, contributes to its biological relevance, particularly in studies involving peptide synthesis and drug development. Overall, N-a-methyl-D-leucine benzyl ester p-tosylate is a versatile compound in the field of medicinal chemistry and peptide synthesis.
Formula:C21H29NO5S
InChI:InChI=1S/C14H21NO2.C7H8O3S/c1-11(2)9-14(3,15)13(16)17-10-12-7-5-4-6-8-12;1-6-2-4-7(5-3-6)11(8,9)10/h4-8,11H,9-10,15H2,1-3H3;2-5H,1H3,(H,8,9,10)/t14-;/m1./s1
SMILES:CC(C)C[C@](C)(C(=O)OCc1ccccc1)N.Cc1ccc(cc1)S(=O)(=O)O
Synonyms:- H-D-N-Me-Leu-OBzl・TosOH
- Benzyl 2-methyl-D-leucinate 4-methylbenzenesulfonate (1:1)
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