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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-Ornithine,N2-[(1,1-dimethylethoxy)carbonyl]-N5-[(2-propen-1-yloxy)carbonyl]-

C=CCOC(=O)NCCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: L-Ornithine,N2-[(1,1-dimethylethoxy)carbonyl]-N5-[(2-propen-1-yloxy)carbonyl]-
CAS Number: 171820-74-9
Product Number: AG003OI3(AGN-PC-0Q9Y4L)
Synonyms:
MDL No:
Molecular Formula: C14H24N2O6
Molecular Weight: 316.3502

Identification/Properties

Properties
MP:
504.9 °C at 760 mmHg
BP:
504.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
316.354g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
11
Exact Mass:
316.163g/mol
Monoisotopic Mass:
316.163g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
403
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-Orn(Aloc)-OH, also known as Nα-Fmoc-L-ornithine, is a key intermediate utilized in chemical synthesis processes to introduce the ornithine amino acid into peptide sequences. Its application lies in the solid-phase peptide synthesis (SPPS) approach, particularly in the Fmoc strategy, where the Boc-Orn(Aloc)-OH serves as a building block for the construction of complex peptide structures.In peptide synthesis, Boc-Orn(Aloc)-OH acts as a protected form of ornithine, facilitating controlled incorporation of this specific amino acid into the peptide chain. The Boc (tert-butyloxycarbonyl) and Aloc (allyloxycarbonyl) protecting groups shield the amine and hydroxyl functionalities of ornithine, allowing selective deprotection steps during peptide elongation while preserving the integrity of the sequence.By using Boc-Orn(Aloc)-OH in Fmoc-based SPPS, chemists can strategically introduce ornithine residues at desired positions within the peptide backbone, enabling the synthesis of peptides with tailored properties and functionalities. This versatile building block plays a crucial role in the precise assembly of peptides for various applications in drug discovery, biochemical research, and biotechnological developments.