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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)-

Benzenepropanamide, a-(acetylamino)-4-hydroxy-, (aS)-

NC(=O)[C@@H](Cc1ccc(cc1)O)NC(=O)C Request for Quotation
Chemical Name: Benzenepropanamide, a-(acetylamino)-4-hydroxy-, (aS)-
CAS Number: 1948-71-6
Product Number: AG003SP4(AGN-PC-0QN7QV)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O3
Molecular Weight: 222.2405

Identification/Properties

Properties
MP:
223-225 °C(lit.)
BP:
582.8°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Refractive Index:
1.5700 (estimate)
Computed Properties
Molecular Weight:
222.244g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
222.1g/mol
Monoisotopic Mass:
222.1g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
260
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

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Chemical Structure


(S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound, also known as $name$, serves as a crucial building block in the creation of various pharmaceuticals, organic chemicals, and biologically active compounds.In chemical synthesis, (S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide acts as a chiral starting material, enabling the production of enantiomerically pure compounds with specific biological activities. Its structure contains both an amide group and a hydroxyphenyl moiety, providing opportunities for diverse chemical reactions and functional group transformations.The presence of a chiral center in (S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide allows for the synthesis of optically active compounds, essential in drug development and medicinal chemistry. By incorporating this compound into synthetic pathways, chemists can control the stereochemistry of the final products, influencing their biological properties and pharmacological profiles.Furthermore, (S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide can participate in various reactions such as acylation, amidation, and condensation, making it a valuable intermediate in the synthesis of diverse chemical entities. Its unique structure and reactivity make it a key component in the construction of complex molecules with specific functionalities, making it indispensable in modern chemical synthesis strategies.