1. Home
  2. 5-Pyrimidinecarboxamide, 4-amino-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-Pyrimidinecarboxamide, 4-amino-

NC(=O)c1cncnc1N Request for Quotation
Chemical Name: 5-Pyrimidinecarboxamide, 4-amino-
CAS Number: 4786-51-0
Product Number: AG00DC5K(AGN-PC-0JWIHV)
Synonyms:
MDL No:
Molecular Formula: C5H6N4O
Molecular Weight: 138.1273

Identification/Properties

Computed Properties
Molecular Weight:
138.13g/mol
XLogP3:
-0.7
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:
94.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
138
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302+H312+H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Aminopyrimidine-5-carboxamide, also known as Aminopyrimidinecarboxamide, is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a key intermediate in the production of various pharmaceuticals, agrochemicals, and organic compounds.In chemical synthesis, 4-Aminopyrimidine-5-carboxamide serves as a crucial building block for the synthesis of diverse heterocyclic compounds due to its unique structure and reactivity. It can undergo various chemical transformations such as acylation, alkylation, and condensation reactions to generate structurally complex molecules with potential biological activities.One of the main uses of 4-Aminopyrimidine-5-carboxamide is in the synthesis of antiviral and anticancer agents where its incorporation into the molecular scaffold imparts desired pharmacological properties. Additionally, its involvement in the construction of herbicides and pesticides highlights its significance in the agricultural sector.Moreover, the versatility of 4-Aminopyrimidine-5-carboxamide extends to the field of material science where it can be employed as a precursor for the synthesis of functional materials and polymers with tailored properties.Overall, the application of 4-Aminopyrimidine-5-carboxamide in chemical synthesis underscores its importance as a valuable synthetic tool for the creation of diverse compounds with potential applications in medicinal, agricultural, and materials science industries.