N-benzyloxycarbonyl-L-asparatic acid 2-allyl ester, CAS No. 99793-10-9

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99793-10-9

Catalog No. EBD696805

CAS 99793-10-9

Name N-benzyloxycarbonyl-L-asparatic acid 2-allyl ester

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Basic Information

Synonyms: L-Asparticacid,N-[(phenylmethoxy)carbonyl]-,4-(2-propen-1-yl)ester L-Asparticacid,N-[(phenylmethoxy)carbonyl]-,4-(2-propenyl)ester(9CI) b-AllylN-(benzyloxycarbonyl)aspartate N-benzyloxycarbonyl-L-asparaticacid2-allylester 2-allylN-Z-(S)-aspartate z-l-asparticacidβ-allylester cbz-l-asparticacid.beta.-allylester (s)-4-(allyloxy)-2-(benzyloxycarbonylamino)-4-oxobutanoicacid Cbz-Asp(OAll)-OH

Molecular Formula: C15H17NO6

Molecular Weight: 307.3

Categories: Medicinal Chemistry > Biochemicals and Life Science Reagents > Amino Acids and Derivatives Synthetic Chemistry > Organic Building Blocks > Carboxylic Acids and Esters

Product Description:

Z-L-Aspartic acid is a protected derivative of the natural amino acid L-aspartic acid. The Z-group (benzyloxycarbonyl) serves as a common amine-protecting group in peptide synthesis, making this compound a crucial building block. It is a white to off-white crystalline powder with a molecular formula of C12H13NO6. Its primary application is in the field of peptide chemistry and pharmaceutical research. As a protected amino acid, it is extensively used in the solid-phase and solution-phase synthesis of peptides and proteins, particularly for incorporating aspartic acid residues while preventing unwanted side reactions. It is also employed in the preparation of aspartame analogs and other bioactive compounds. This reagent is valued for its high purity and stability, which are essential for reproducible synthetic outcomes. It should be stored in a cool, dry place and handled with standard laboratory precautions to avoid inhalation or skin contact.

Physical Properties