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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)-

2-Pyrimidinecarboximidamide, N-hydroxy-

O/N=C(c1ncccn1)/N Request for Quotation
Chemical Name: 2-Pyrimidinecarboximidamide, N-hydroxy-
CAS Number: 90993-49-0
Product Number: AG00GRNL(AGN-PC-0OMIRY)
Synonyms:
MDL No:
Molecular Formula: C5H6N4O
Molecular Weight: 138.1273

Identification/Properties

Computed Properties
Molecular Weight:
138.13g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
138.054g/mol
Monoisotopic Mass:
138.054g/mol
Topological Polar Surface Area:
84.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-HYDROXY-2-PYRIMIDINECARBOXIMIDAMIDE is a versatile chemical compound widely utilized in chemical synthesis as a key intermediate. Its unique structure and reactivity make it a valuable tool for organic chemists in various applications.Within chemical synthesis, N-HYDROXY-2-PYRIMIDINECARBOXIMIDAMIDE serves as a crucial building block for the construction of complex molecules. Its hydroxy and carboxylic acid functionalities enable it to participate in a range of chemical reactions, such as acylation, amidation, and esterification. This compound's reactivity allows for the introduction of pyrimidine and amide moieties into target molecules, facilitating the synthesis of diverse organic compounds.One of the primary applications of N-HYDROXY-2-PYRIMIDINECARBOXIMIDAMIDE is in the production of pharmaceuticals and agrochemicals. By incorporating this compound into synthetic pathways, chemists can access novel drug candidates, crop protection agents, and other biologically active compounds. The versatility of N-HYDROXY-2-PYRIMIDINECARBOXIMIDAMIDE enables researchers to tailor its use to specific synthetic needs, making it a valuable asset in the design and development of new chemical entities.Furthermore, N-HYDROXY-2-PYRIMIDINECARBOXIMIDAMIDE demonstrates excellent compatibility with a variety of reaction conditions and functional groups, enhancing its utility in complex synthesis routes. Its stability and ease of handling further contribute to its widespread adoption in both academic research and industrial settings.In summary, N-HYDROXY-2-PYRIMIDINECARBOXIMIDAMIDE plays a crucial role in chemical synthesis by serving as a versatile and reactive intermediate for the construction of complex organic molecules. Its applications in pharmaceutical and agrochemical research highlight its significance in advancing the field of organic chemistry.