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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)-

Z-Nva-OH

CCC[C@@H](C(=O)O)NC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: Z-Nva-OH
CAS Number: 21691-44-1
Product Number: AG006ZZP(AGN-PC-0WAFI1)
Synonyms:
MDL No:
Molecular Formula: C13H17NO4
Molecular Weight: 251.2784

Identification/Properties

Computed Properties
Molecular Weight:
251.282g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
251.116g/mol
Monoisotopic Mass:
251.116g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
274
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Z-Nva-OH, or Z-norvaline hydrochloride, plays a crucial role in chemical synthesis as a versatile building block compound. This compound is widely utilized in peptide synthesis, particularly in the solid-phase peptide synthesis (SPPS) methodology. Z-Nva-OH serves as a valuable amino acid derivative due to its unique properties and functionalities, making it a popular choice for peptide chemists and researchers.In chemical synthesis, Z-Nva-OH is commonly used as a key intermediate for preparing various peptides with specific sequences and structures. Its ability to act as a protected amino acid enables chemists to incorporate it into peptide chains with precision and control. Additionally, Z-Nva-OH is known for its compatibility with other amino acids and coupling reagents, allowing for efficient and reliable peptide assembly processes.Moreover, Z-Nva-OH exhibits excellent stability under typical peptide synthesis conditions, ensuring reliable performance and consistent results. Its specific chemical structure and reactivity make it an essential component in the creation of complex peptides for pharmaceutical, biotechnological, and research purposes. Overall, Z-Nva-OH is a valuable tool in chemical synthesis, enabling the synthesis of a wide range of peptides with diverse functionalities and applications.