CAS 59587-94-9

(4S)-4-[(tert-butoxycarbonyl)amino]-5-oxo-5-phenoxypentanoic acid (non-preferred name)

Description:

The chemical substance known as (4S)-4-[(tert-butoxycarbonyl)amino]-5-oxo-5-phenoxypentanoic acid, with the CAS number 59587-94-9, is an amino acid derivative characterized by its complex structure that includes a phenoxy group and a tert-butoxycarbonyl (Boc) protecting group. This compound features a pentanoic acid backbone, which contributes to its acidic properties. The presence of the Boc group indicates that it is likely used in peptide synthesis as a protecting group for the amino functionality, allowing for selective reactions without interfering with the amine. The phenoxy group adds to its hydrophobic character, influencing its solubility and interaction with biological systems. The stereochemistry at the 4-position, denoted as (4S), suggests that this compound has specific spatial arrangements that may affect its biological activity and interactions. Overall, this compound is of interest in medicinal chemistry and peptide synthesis due to its structural features and potential applications in drug development.

Formula: C₁₆H₂₁NO₆

InChI: InChI=1/C16H21NO6/c1-16(2,3)23-15(21)17-12(9-10-13(18)19)14(20)22-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,19)/t12-/m0/s1

Synonyms:

• Boc-Glu-Phenyl Ester

Boc-Glu-phenyl ester

CAS: 59587-94-9

Bachem ID: 4029196.

Formula: C₁₆H₂₁NO₆

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 332.35

Ref: 01-4029196

Boc-glu-phenyl ester

CAS: 59587-94-9

Formula: C₁₆H₂₁NO₆

Molecular weight: 323.341

Ref: IN-DA003OGX

(S)-4-((tert-Butoxycarbonyl)amino)-5-oxo-5-phenoxypentanoic acid

CAS: 59587-94-9

(S)-4-((tert-Butoxycarbonyl)amino)-5-oxo-5-phenoxypentanoic acid

Purity: 97%

Molecular weight: 323.35g/mol

Ref: 54-OR1056815

Boc-Glu-OPh

CAS: 59587-94-9

Molecular weight: 323.34

Ref: 7W-GM9341

Boc-Glu-phenyl ester

CAS: 59587-94-9

Boc-Glu-phenyl ester is an inhibitor of bacterial protein synthesis. It was first synthesized as a synthetic substrate for the enzyme staphylococcal protease and has been shown to be active against both human and staphylococcal cells, with activity against strains resistant to other antibiotics. Boc-Glu-phenyl ester inhibits the synthesis of proteins by binding to the catalytic site of the enzyme and preventing formation of peptide bonds. This inhibition leads to cell death due to a lack of critical proteins required for cellular function. Boc-Glu-phenyl ester is also specific for staphylococci, which may be due to its ability to inhibit the production of epidermolytic exotoxins.

Formula: C₁₆H₂₁NO₆

Purity: Min. 95%

Molecular weight: 323.34 g/mol

Ref: 3D-FB111274