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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)-

Pentanamide, 2-amino-5-[(aminoiminomethyl)amino]-, (R)-

NN=CNCCC[C@H](C(=O)N)N Request for Quotation
Chemical Name: Pentanamide, 2-amino-5-[(aminoiminomethyl)amino]-, (R)-
CAS Number: 203308-91-2
Product Number: AG0028T6(AGN-PC-0O7A2Q)
Synonyms:
MDL No:
Molecular Formula: C6H15N5O
Molecular Weight: 173.2162

Identification/Properties

Properties
BP:
447.7°C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
246.136g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
245.081g/mol
Monoisotopic Mass:
245.081g/mol
Topological Polar Surface Area:
134A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
175
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

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


H-D-Arg-NH2, also known as Nα,Nα-Dibenzyl-D-argininamide, is a key component in chemical synthesis processes. This compound is frequently employed in peptide synthesis and solid-phase peptide synthesis due to its unique properties and versatile applications. H-D-Arg-NH2 serves as a valuable building block for creating various peptides with specific sequences and functions. Its use in chemical synthesis allows for the precise incorporation of arginine residues into peptides, enabling researchers to study the role of arginine in biological systems and develop novel peptide-based therapeutics. Peptide synthesis utilizing H-D-Arg-NH2 enables the production of customized peptides for a wide range of applications, including drug development, biochemical research, and biotechnology. By incorporating H-D-Arg-NH2 into the synthesis process, chemists can efficiently and effectively produce complex peptides with high purity and structural integrity.