1. Home
  2. 1H-Imidazole-4,5-dicarboxamide

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-4,5-dicarboxamide

NC(=O)c1[nH]cnc1C(=O)N Request for Quotation
Chemical Name: 1H-Imidazole-4,5-dicarboxamide
CAS Number: 83-39-6
Product Number: AG003QZN(AGN-PC-0JL6TD)
Synonyms:
MDL No:
Molecular Formula: C5H6N4O2
Molecular Weight: 154.1267

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
154.129g/mol
XLogP3:
-2.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
154.049g/mol
Monoisotopic Mass:
154.049g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
193
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

Request for Quotation

Customer Feedback

Chemical Structure


1H-Imidazole-4,5-dicarboxamide, also known as 1H-Imidazole-4,5-dicarboxylic acid, is a versatile compound commonly used in chemical synthesis due to its unique chemical properties. In particular, this compound serves as a crucial building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its ability to undergo selective functionalization reactions makes it an essential intermediate in the production of diverse organic compounds. When employed in chemical reactions, 1H-Imidazole-4,5-dicarboxamide facilitates the formation of complex molecular structures, allowing for the creation of novel compounds with desirable properties. Its role in chemical synthesis extends to the development of new drugs, advanced materials, and specialized chemicals, highlighting its significance in modern organic chemistry.