Z-L-aspartic acid β-allyl ester
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Z-L-aspartic acid β-allyl ester

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Category
CBZ-Amino Acids
Catalog number
BAT-007758
CAS number
99793-10-9
Molecular Formula
C15H17NO6
Molecular Weight
307.30
Z-L-aspartic acid β-allyl ester
IUPAC Name
(2S)-4-oxo-2-(phenylmethoxycarbonylamino)-4-prop-2-enoxybutanoic acid
Synonyms
Z-L-Asp(OAll)-OH; Z-L-aspartic acid b-allyl ester; Z-Asp(OAll)-OH; (S)-4-(Allyloxy)-2-(((benzyloxy)carbonyl)amino)-4-oxobutanoic acid; Z-L-aspartic acid ss-allyl ester; N-(Benzyloxycarbonyl)-L-aspartic acid 4-allyl ester; L-Aspartic acid, N-[(phenylmethoxy)carbonyl]-, 4-(2-propen-1-yl) ester
Appearance
White powder
Purity
≥95%
Density
1.3±0.1 g/cm3
Boiling Point
517.5±50.0°C at 760 mmHg
Storage
Store at 2-8°C
InChI
InChI=1S/C15H17NO6/c1-2-8-21-13(17)9-12(14(18)19)16-15(20)22-10-11-6-4-3-5-7-11/h2-7,12H,1,8-10H2,(H,16,20)(H,18,19)/t12-/m0/s1
InChI Key
LKXLDZQGKGEICY-LBPRGKRZSA-N
Canonical SMILES
C=CCOC(=O)CC(C(=O)O)NC(=O)OCC1=CC=CC=C1

Z-L-aspartic acid β-allyl ester is a versatile compound with varied applications in bioscience and biotechnology. Here are some key applications of Z-L-aspartic acid β-allyl ester:

Peptide Synthesis: Z-L-aspartic acid β-allyl ester is used as a protecting group in peptide synthesis. It helps in the selective protection of the amino group, ensuring precise peptide chain elongation. This enables the synthesis of complex peptides and proteins with high purity and accuracy.

Pharmaceutical Research: This compound is valuable in the development of new drugs and therapeutic peptides. By enabling the synthesis of bioactive peptides, researchers can design and evaluate potential drug candidates. This application is crucial for the discovery of new treatments for various diseases, including cancer and infectious diseases.

Enzyme Inhibition Studies: Z-L-aspartic acid β-allyl ester can be employed in the design of enzyme inhibitors. By incorporating it into specific chemical structures, researchers can study its interactions with target enzymes. This assists in the identification of potent inhibitors for therapeutic applications and understanding enzyme kinetics.

Biocatalysis: In biotechnological processes, Z-L-aspartic acid β-allyl ester can be used as a substrate or intermediate. It plays a role in the synthesis of optically pure amino acids and other valuable compounds. This supports the development of efficient biocatalytic processes for industrial applications.

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