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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)-

D-Tyrosine, N-[(phenylmethoxy)carbonyl]-

O=C(N[C@@H](C(=O)O)Cc1ccc(cc1)O)OCc1ccccc1 Request for Quotation
Chemical Name: D-Tyrosine, N-[(phenylmethoxy)carbonyl]-
CAS Number: 64205-12-5
Product Number: AG003VDL(AGN-PC-0OELY7)
Synonyms:
MDL No:
Molecular Formula: C17H17NO5
Molecular Weight: 315.3206

Identification/Properties

Properties
MP:
99 °C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
315.325g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
315.111g/mol
Monoisotopic Mass:
315.111g/mol
Topological Polar Surface Area:
95.9A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
386
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#:
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


(R)-2-(((Benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid, known for short as $name$, is a key compound utilized in chemical synthesis for its versatile applications. This compound plays a crucial role in peptide synthesis, specifically in the construction of peptide linkages through amide bond formation. Its unique structure containing a protected amino group, a hydroxyphenyl group, and a propanoic acid moiety allows for precise control over peptide bond formation during the synthesis process.In the realm of chemical synthesis, (R)-2-(((Benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid serves as a pivotal building block for the creation of peptide-based pharmaceuticals, bioconjugates, and specialty chemicals. By incorporating this compound into synthetic pathways, chemists can efficiently access a wide range of peptide derivatives with tailored functionalities and properties.Additionally, the selective deprotection of the benzyloxycarbonyl group in (R)-2-(((Benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid enables further structural modifications and derivatization, expanding its utility in the creation of structurally diverse peptides and peptidomimetics. This flexibility in functional group manipulations makes (R)-2-(((Benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid a valuable asset in the arsenal of synthetic chemists seeking to access complex peptide structures with precision and efficiency.