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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-Serine, O-amino-

NC(C(=O)O)CON Request for Quotation
Chemical Name: L-Serine, O-amino-
CAS Number: 1187-83-3
Product Number: AG003GCT(AGN-PC-0NZOOG)
Synonyms:
MDL No:
Molecular Formula: C3H8N2O3
Molecular Weight: 120.1072

Identification/Properties

Properties
BP:
372.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


2-Amino-3-(aminooxy)propanoic acid, also known as AOA, is a versatile compound widely utilized in chemical synthesis. Its unique structure containing both an amino group and an aminooxy group makes it a valuable building block in organic chemistry. One of the key applications of 2-Amino-3-(aminooxy)propanoic acid is in the synthesis of peptide conjugates. By selectively modifying the amino and aminooxy functional groups, chemists can create peptide-drug conjugates or peptide-polymer conjugates with enhanced properties such as improved stability, solubility, or targeted delivery.In addition, 2-Amino-3-(aminooxy)propanoic acid can be used in the preparation of various bioconjugates for biological studies. Its ability to connect to biomolecules through either the amino or aminooxy group allows for the creation of complex structures for investigating biological interactions or developing new bioactive compounds.Furthermore, this compound is employed in the synthesis of fluorescent probes and labeling reagents. By attaching fluorescent moieties to 2-Amino-3-(aminooxy)propanoic acid, researchers can design molecular probes for tracking biological processes or labeling specific molecules for visualization purposes.Overall, the versatility of 2-Amino-3-(aminooxy)propanoic acid in chemical synthesis makes it a valuable tool for creating diverse compounds with applications in drug development, materials science, and biological research.