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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)-

5-amino-1,2-oxazole-4-carboxamide;sulfuric acid

OS(=O)(=O)O.NC(=O)c1cnoc1N Request for Quotation
Chemical Name: 5-amino-1,2-oxazole-4-carboxamide;sulfuric acid
CAS Number: 1273577-24-4
Product Number: AG000WYE(AGN-PC-0BLD50)
Synonyms:
MDL No: MFCD16495885
Molecular Formula: C4H7N3O6S
Molecular Weight: 225.1799

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Aminoisoxazole-4-carboxamide Hydrogensulfate, also known as AICA ribonucleotide, is a key compound used in chemical synthesis for various applications. This chemical plays a crucial role in the development of pharmaceuticals and biologically active molecules. Specifically, it serves as a potent intermediate in the synthesis of nucleotide analogs and other pharmaceutical compounds.In chemical synthesis, 5-Aminoisoxazole-4-carboxamide Hydrogensulfate is utilized as a building block for the creation of nucleoside analogs, such as acyclovir and ribavirin, which are important antiviral medications. Additionally, this compound is employed in the preparation of nucleotide derivatives that can modulate various biological pathways and enzyme activities.Moreover, 5-Aminoisoxazole-4-carboxamide Hydrogensulfate is valued for its ability to mimic natural nucleosides and interfere with nucleic acid synthesis, making it a versatile tool in drug discovery and medicinal chemistry. Its unique structure and reactivity make it a valuable component in the synthesis of novel pharmaceuticals with diverse therapeutic applications.