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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-(R)-3-Amino-4-(3-cyano-phenyl)-butyric acid

N#Cc1cccc(c1)C[C@@H](NC(=O)OC(C)(C)C)CC(=O)O Request for Quotation
Chemical Name: Boc-(R)-3-Amino-4-(3-cyano-phenyl)-butyric acid
CAS Number: 269726-83-2
Product Number: AG0034JE(AGN-PC-0O8GZ5)
Synonyms:
MDL No:
Molecular Formula: C16H20N2O4
Molecular Weight: 304.3410

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
304.346g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
304.142g/mol
Monoisotopic Mass:
304.142g/mol
Topological Polar Surface Area:
99.4A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
447
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

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 (R)-3-((tert-Butoxycarbonyl)amino)-4-(3-cyanophenyl)butanoic acid, commonly referred to as $name$, is a valuable compound widely utilized in chemical synthesis processes. It serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its versatile reactivity and structural properties. Specifically, in chemical synthesis, $name$ is frequently employed as a key intermediate for the production of specialized peptides and amino acid derivatives.One of the significant applications of (R)-3-((tert-Butoxycarbonyl)amino)-4-(3-cyanophenyl)butanoic acid is as a chiral auxiliary in asymmetric synthesis. Its chiral nature enables the selective control of stereochemistry in forming complex molecules, making it a valuable tool in the synthesis of enantiopure compounds. By incorporating $name$ into the synthetic pathway, chemists can achieve high levels of enantioselectivity, crucial for producing biologically active compounds and fine chemicals with specific functionalities.Moreover, (R)-3-((tert-Butoxycarbonyl)amino)-4-(3-cyanophenyl)butanoic acid can participate in various coupling reactions, such as amide bond formation and peptide synthesis. Its functional groups allow for efficient chemical transformations, facilitating the construction of peptide sequences and peptide mimetics. This versatility makes $name$ an essential component in the creation of peptide-based drugs, as well as in the modification and functionalization of peptides for research purposes.In summary, the application of (R)-3-((tert-Butoxycarbonyl)amino)-4-(3-cyanophenyl)butanoic acid in chemical synthesis extends to its role as a critical intermediate for generating chiral compounds, controlling stereochemistry, and enabling the synthesis of peptides and amino acid derivatives with precision and efficiency.