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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-Tyrosine, L-phenylalanyl-

OC(=O)[C@H](Cc1ccc(cc1)O)NC(=O)[C@H](Cc1ccccc1)N Request for Quotation
Chemical Name: L-Tyrosine, L-phenylalanyl-
CAS Number: 17355-18-9
Product Number: AG001Z12(AGN-PC-0O4WTI)
Synonyms:
MDL No:
Molecular Formula: C18H20N2O4
Molecular Weight: 328.3624

Identification/Properties

Computed Properties
Molecular Weight:
328.368g/mol
XLogP3:
-1.7
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
328.142g/mol
Monoisotopic Mass:
328.142g/mol
Topological Polar Surface Area:
113A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
415
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

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P264-P270-P301+P310+P330-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (S)-2-((S)-2-Amino-3-phenylpropanamido)-3-(4-hydroxyphenyl)propanoic acid in chemical synthesis is primarily focused on its use as a chiral building block. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals where stereochemistry plays a crucial role in determining the biological activity and properties of the final product. By incorporating this chiral entity into the molecular structure of target compounds, chemists can access enantiomerically pure substances with enhanced selectivity and potency. The presence of both an amino group and a hydroxyphenyl group in the molecule provides versatility in functional group transformations, enabling the creation of diverse molecular architectures with specific stereochemical arrangements. In addition, the (S)-2-((S)-2-Amino-3-phenylpropanamido)-3-(4-hydroxyphenyl)propanoic acid can also act as a ligand in asymmetric catalysis, facilitating the creation of new stereoselective synthetic methodologies. Its wide-ranging synthetic utility makes it a valuable tool for organic chemists working in the field of medicinal chemistry, organic synthesis, and chemical biology.