4-[[2-[[2-[[(2S)-1-(4-nitroanilino)-1-oxo-3-phenylpropan-2-yl]amino]-2-oxoethyl]amino]-2-oxoethyl]amino]-4-oxobutanoic acid


Chemical Name: 4-[[2-[[2-[[(2S)-1-(4-nitroanilino)-1-oxo-3-phenylpropan-2-yl]amino]-2-oxoethyl]amino]-2-oxoethyl]amino]-4-oxobutanoic acid
CAS Number: 68982-90-1
Product Number: AG005ZFV(AGN-PC-05WXMM)
Synonyms:
MDL No: MFCD00038721
Molecular Formula: C23H25N5O8
Molecular Weight: 499.4733

Identification/Properties


Properties
MP:
202 - 205°C
Storage:
-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
499.48g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
12
Exact Mass:
499.17g/mol
Monoisotopic Mass:
499.17g/mol
Topological Polar Surface Area:
200A^2
Heavy Atom Count:
36
Formal Charge:
0
Complexity:
801
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



The compound N-(3-Carboxy-1-oxopropyl)glycylglycyl-N-(4-nitrophenyl)-L-phenylalaninamide serves as a versatile building block in chemical synthesis processes. Its unique molecular structure allows for precise manipulation and controlled reactivity in forming complex peptide chains and molecular assemblies. This compound is particularly valuable in peptide synthesis due to its ability to introduce specific functional groups and stereochemical features into the target molecules. By incorporating N-(3-Carboxy-1-oxopropyl)glycylglycyl-N-(4-nitrophenyl)-L-phenylalaninamide into synthetic pathways, chemists can achieve tailored modifications and create bioactive peptides with enhanced properties for various applications in pharmaceuticals, materials science, and biotechnology.