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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)-

1H-Imidazole-5-carboxamide, N,1-dimethyl-4-(methylamino)-

CNC(=O)c1n(C)cnc1NC Request for Quotation
Chemical Name: 1H-Imidazole-5-carboxamide, N,1-dimethyl-4-(methylamino)-
CAS Number: 20041-90-1
Product Number: AG00C3BE(AGN-PC-0JPMGL)
Synonyms:
MDL No:
Molecular Formula: C7H12N4O
Molecular Weight: 168.1964

Identification/Properties

Computed Properties
Molecular Weight:
168.2g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
168.101g/mol
Monoisotopic Mass:
168.101g/mol
Topological Polar Surface Area:
59A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
173
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,1-Dimethyl-4-(methylamino)-1H-imidazole-5-carboxamide is a versatile chemical compound widely utilized in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals and agrochemicals due to its unique structural properties and reactivity. Its functional groups enable it to participate in a range of synthetic reactions, making it an essential component in the production of complex organic molecules. Its application in chemical synthesis extends to the formation of heterocyclic compounds, amino acids, peptide bond formations, and as a precursor in the development of novel drug candidates. Additionally, its presence in the synthesis process often enhances the efficiency and selectivity of reactions, making it a valuable tool in organic chemistry.