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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)-

Boc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid

N#Cc1ccc(cc1)C[C@H](NC(=O)OC(C)(C)C)CC(=O)O Request for Quotation
Chemical Name: Boc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid
CAS Number: 270065-89-9
Product Number: AG003OEY(AGN-PC-0O8H5Y)
Synonyms:
MDL No:
Molecular Formula: C16H20N2O4
Molecular Weight: 304.3410

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-3-((tert-Butoxycarbonyl)amino)-4-(4-cyanophenyl)butanoic acid, often referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it an indispensable component in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals.$name$ can be utilized in the synthesis of peptide-based compounds due to its ability to act as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) protecting group ensures the selective reaction of the primary amine, allowing for controlled peptide bond formation. This characteristic makes $name$ particularly valuable in solid-phase peptide synthesis and in the production of peptide mimetics with enhanced stability and bioavailability.Furthermore, $name$ serves as a key intermediate in the preparation of diverse bioactive molecules with therapeutic potential. Its cyanophenyl functionality enables the construction of complex molecular structures through various chemical transformations, such as Suzuki coupling reactions, amide bond formations, and ketone reductions. This flexibility opens up a wide range of synthetic pathways for the creation of pharmaceutical candidates and research compounds.In summary, the application of (S)-3-((tert-Butoxycarbonyl)amino)-4-(4-cyanophenyl)butanoic acid in chemical synthesis encompasses its pivotal role as a building block for peptide synthesis and its significance in the development of bioactive molecules with medicinal and research applications.