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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, N-acetyl-

OC(=O)[C@H](Cc1ccc(cc1)O)NC(=O)C Request for Quotation
Chemical Name: L-Tyrosine, N-acetyl-
CAS Number: 2901-77-1
Product Number: AG002V78(AGN-PC-0O8N6Q)
Synonyms:
MDL No:
Molecular Formula: C11H13NO4
Molecular Weight: 223.2252

Identification/Properties

Computed Properties
Molecular Weight:
223.22g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
223.084458g/mol
Monoisotopic Mass:
223.084458g/mol
Topological Polar Surface Area:
86.6Ų
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
259
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-Acetamido-3-(4-hydroxyphenyl)propanoic acid, also known as $name$, serves as a valuable reagent in chemical synthesis. With its unique chemical structure, this compound is frequently employed in the pharmaceutical industry for the creation of novel drug molecules. Specifically, its functional groups make it ideal for use in the synthesis of various bioactive compounds, such as inhibitors and pharmaceutical intermediates. By leveraging the versatility of this compound in organic reactions, chemists can access a wide range of synthetic pathways to develop new drug candidates with potential therapeutic benefits. Additionally, the presence of the hydroxyphenyl group in 2-Acetamido-3-(4-hydroxyphenyl)propanoic acid enhances its interactions with biological targets, making it a promising building block for designing biologically active molecules.