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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)-

L-Arginine, N2-[(1,1-dimethylethoxy)carbonyl]-, monohydrochloride,monohydrate

OC(=O)[C@@H](NC(=O)OC(C)(C)C)CCCNC(=N)N.O.Cl Request for Quotation
Chemical Name: L-Arginine, N2-[(1,1-dimethylethoxy)carbonyl]-, monohydrochloride,monohydrate
CAS Number: 114622-81-0
Product Number: AG000EUK(AGN-PC-0P6IUB)
Synonyms:
MDL No:
Molecular Formula: C11H25ClN4O5
Molecular Weight: 328.7930

Identification/Properties

Properties
MP:
176-178°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
328.794g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
328.151g/mol
Monoisotopic Mass:
328.151g/mol
Topological Polar Surface Area:
141A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
345
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N2-Boc-L-arginine Hydrochloride Hydrate is a versatile compound widely utilized in chemical synthesis for its unique properties and numerous applications. This compound serves as a crucial building block in peptide synthesis, particularly in the production of peptides with pharmaceutical potential. By incorporating N2-Boc-L-arginine Hydrochloride Hydrate into peptide sequences, chemists can enhance the stability, solubility, and biological activity of the resulting molecules.Moreover, the use of N2-Boc-L-arginine Hydrochloride Hydrate in chemical synthesis enables precise control over the structure and function of peptides, thereby facilitating the development of novel drugs, bioactive molecules, and research tools. Its compatibility with a variety of coupling reagents and protective groups makes it a valuable asset in synthetic organic chemistry, allowing for efficient and selective modifications during peptide assembly. In addition, its hygroscopic nature and stability in solution offer practical advantages for synthetic processes, ensuring reliable and reproducible results.Overall, N2-Boc-L-arginine Hydrochloride Hydrate plays a crucial role in advancing the field of chemical synthesis by facilitating the creation of complex peptides and bioactive compounds with tailored properties and functions. Its widespread applications in peptide chemistry underscore its significance as a key component in the realm of drug discovery, biomedical research, and chemical biology.