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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

L-Leucine, L-phenylalanyl-

N[C@H](C(=O)N[C@H](C(=O)O)CC(C)C)Cc1ccccc1 Request for Quotation
Chemical Name: L-Leucine, L-phenylalanyl-
CAS Number: 3303-55-7
Product Number: AG00I6CV(AGN-PC-0O8ZCG)
Synonyms:
MDL No:
Molecular Formula: C15H22N2O3
Molecular Weight: 278.3468

Identification/Properties

Computed Properties
Molecular Weight:
278.352g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
278.163g/mol
Monoisotopic Mass:
278.163g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
325
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

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Chemical Structure


H-Phe-Leu-OH, also known as N-(3-phenylpropyl)-L-leucine, is a dipeptide used in chemical synthesis for a variety of applications. This compound is frequently utilized in peptide synthesis as a building block for creating larger peptide chains with specific sequences. H-Phe-Leu-OH can be incorporated into peptides to introduce structural diversity and alter properties such as solubility, stability, and bioactivity. In addition, this dipeptide can serve as a valuable tool in drug discovery and development processes, playing a crucial role in designing and studying novel peptide-based therapeutics. Its unique chemical structure and reactivity make H-Phe-Leu-OH a versatile and essential component in the realm of chemical synthesis.