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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)-

(R)-5-Amino-5-phenylpentanoic acid hydrochloride

N[C@@H](c1ccccc1)CCCC(=O)O.Cl Request for Quotation
Chemical Name: (R)-5-Amino-5-phenylpentanoic acid hydrochloride
CAS Number: 1810074-59-9
Product Number: AG0022KT(AGN-PC-0WAM9K)
Synonyms:
MDL No:
Molecular Formula: C11H16ClNO2
Molecular Weight: 229.7032

Identification/Properties

Computed Properties
Molecular Weight:
229.704g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
229.087g/mol
Monoisotopic Mass:
229.087g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
176
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-5-Amino-5-phenylpentanoic acid hydrochloride is a valuable compound in chemical synthesis due to its chirality and unique structural properties. This compound serves as a versatile building block in the creation of pharmaceuticals, agrochemicals, and fine chemicals. Its chiral nature allows for the development of enantiopure compounds, which are crucial in drug discovery and development processes. Furthermore, the presence of the amino and phenyl functional groups in the molecule provides diverse reactivity, enabling it to participate in various synthetic transformations such as amidation, cyclization reactions, and coupling reactions. This compound is particularly useful in the synthesis of peptide-based drugs, where the chirality and functional groups play a critical role in determining biological activity and pharmacological properties.