CAS 5618-98-4

N-[(Phenylmethoxy)carbonyl]tyrosine

Description:

N-[(Phenylmethoxy)carbonyl]tyrosine, also known by its CAS number 5618-98-4, is a derivative of the amino acid tyrosine, which is characterized by the presence of a phenylmethoxycarbonyl group. This modification enhances its stability and solubility, making it useful in various biochemical applications, particularly in peptide synthesis and drug development. The compound features a phenyl group, which contributes to its hydrophobic characteristics, and a methoxy group that can influence its reactivity and interaction with biological systems. N-[(Phenylmethoxy)carbonyl]tyrosine is typically utilized in the synthesis of peptides where protecting groups are necessary to prevent unwanted reactions during the coupling process. Its structural attributes allow for selective reactions, making it a valuable intermediate in organic synthesis. Additionally, the compound's properties may include moderate to high melting points and solubility in organic solvents, which are common traits for similar amino acid derivatives. Overall, this compound plays a significant role in the field of medicinal chemistry and peptide research.

Formula: C₁₇H₁₇NO₅

InChI: InChI=1/C17H17NO5/c19-14-8-6-12(7-9-14)10-15(16(20)21)18-17(22)23-11-13-4-2-1-3-5-13/h1-9,15,19H,10-11H2,(H,18,22)(H,20,21)/t15-/m0/s1

InChI key: InChIKey=MCRMUCXATQAAMN-UHFFFAOYSA-N

SMILES: C(C(NC(OCC1=CC=CC=C1)=O)C(O)=O)C2=CC=C(O)C=C2

Synonyms:

• Tyrosine, N-carboxy-, N-benzyl ester, DL-
• N-(Carbobenzyloxy)-DL-tyrosine
• DL-Tyrosine, N-[(phenylmethoxy)carbonyl]-
• N-[(Phenylmethoxy)carbonyl]tyrosine
• Tyrosine, N-[(phenylmethoxy)carbonyl]-
• N-[(benzyloxy)carbonyl]-L-tyrosine
• N-Benzyloxycarbonyl-DL-tyrosine
• ((Benzyloxy)carbonyl)tyrosine
• N-Methyl-N-benzyloxycarbonyl-L-Phenylalanine, derivative of
• N-[(Phenylmethoxy)carbonyl]-DL-tyrosine

2-([(Benzyloxy)carbonyl]amino)-3-(4-hydroxyphenyl)propanoic acid

CAS: 5618-98-4

2-([(Benzyloxy)carbonyl]amino)-3-(4-hydroxyphenyl)propanoic acid is a chemical compound that belongs to the class of amino acid derivatives. It has an optical isomer with a different configuration at the chiral centre and has been used as an experiment to study the optical properties of β-cyclodextrin. 2-([(Benzyloxy)carbonyl]amino)-3-(4-hydroxyphenyl)propanoic acid can be separated by chromatography using enantioseparation, which is a technique for separating molecules based on their asymmetric properties. The molecule functions as a cosolvent and transesterification agent in organic solvents. 2-([(Benzyloxy)carbonyl]amino)-3-(4-hydroxyphenyl)propanoic acid can also be synthesized from other compounds, such as acetophenone and benzaldehyde,

Formula: C₁₇H₁₇NO₅

Purity: Min. 95%

Molecular weight: 315.32 g/mol

Ref: 3D-FAA61898