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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)-

methyl 2-amino-4-phenylbutanoate;hydrochloride

COC(=O)C(CCc1ccccc1)N.Cl Request for Quotation
Chemical Name: methyl 2-amino-4-phenylbutanoate;hydrochloride
CAS Number: 85808-33-9
Product Number: AG004RK8(AGN-PC-00KMTY)
Synonyms:
MDL No: MFCD08458513
Molecular Formula: C11H16ClNO2
Molecular Weight: 229.7032

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
229.704g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
229.087g/mol
Monoisotopic Mass:
229.087g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
176
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:
2
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-DL-HoPhe-OMe.HCl is a versatile reagent commonly used in chemical synthesis due to its unique properties and functionality. This compound, a protected form of DL-Homophenylalanine methyl ester hydrochloride, serves as a key building block in the preparation of various peptides and peptidomimetics.In peptide synthesis, H-DL-HoPhe-OMe.HCl is utilized to introduce the DL-homophenylalanine residue into the sequence, imparting specific structural and functional characteristics to the final peptide product. By incorporating this amino acid derivative, researchers can modulate the properties of the peptide, such as enhancing bioactivity, improving stability, or influencing binding affinity.Furthermore, H-DL-HoPhe-OMe.HCl is valuable in the development of peptidomimetics – molecules designed to mimic the structure and function of peptides. Its selective reactivity and compatibility with standard peptide coupling chemistries make it a valuable tool for creating peptidomimetic compounds with tailored properties for various biomedical and pharmaceutical applications.Overall, the application of H-DL-HoPhe-OMe.HCl in chemical synthesis offers researchers a strategic approach to designing and synthesizing peptide-based molecules with desired functionalities and properties.