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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)-

Arginine, N2-[(phenylmethoxy)carbonyl]-

NC(=N)NCCC[C@@H](C(=O)O)NC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: Arginine, N2-[(phenylmethoxy)carbonyl]-
CAS Number: 1234-35-1
Product Number: AG000KIQ(AGN-PC-0O0MUR)
Synonyms:
MDL No:
Molecular Formula: C14H20N4O4
Molecular Weight: 308.3330

Identification/Properties

Properties
MP:
171-174 °C
BP:
448.73°C (rough estimate)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
-10 ° (C=5.5, 0.2mol/L HCl)
Computed Properties
Molecular Weight:
308.338g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
308.148g/mol
Monoisotopic Mass:
308.148g/mol
Topological Polar Surface Area:
140A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
390
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-Arg-OH, also known as Z-Arginine-OH, is a valuable compound widely used in chemical synthesis. This amino acid derivative plays a crucial role in the creation of various peptide molecules through solid-phase peptide synthesis (SPPS) techniques. Its unique structure and properties make Z-Arg-OH an excellent building block for the synthesis of peptides with specific functionalities or structural characteristics. By incorporating Z-Arg-OH into peptide sequences, chemists can introduce a variety of modifications or conjugations to tailor the peptides for a range of research, pharmaceutical, or biotechnological applications.Additionally, Z-Arg-OH can be utilized as a substrate in enzymatic reactions or as a starting material for the synthesis of small organic molecules. Its versatile nature and compatibility with common peptide synthesis methodologies make it an indispensable tool for chemists and researchers looking to design and develop new compounds with precise control over their chemical structure and properties.