1. Home
  2. 4-Pyrimidinecarboxylic acid, 2-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)-

4-Pyrimidinecarboxylic acid, 2-amino-

Nc1nccc(n1)C(=O)O Request for Quotation
Chemical Name: 4-Pyrimidinecarboxylic acid, 2-amino-
CAS Number: 2164-65-0
Product Number: AG003GK1(AGN-PC-0JOJSG)
Synonyms:
MDL No:
Molecular Formula: C5H5N3O2
Molecular Weight: 139.1121

Identification/Properties

Properties
BP:
474.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
139.114g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
139.038g/mol
Monoisotopic Mass:
139.038g/mol
Topological Polar Surface Area:
89.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
139
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


2-Aminopyrimidine-4-carboxylic acid, also known as $name$, is a versatile compound that plays a crucial role in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other organic molecules due to its unique structure and reactivity.In chemical synthesis, 2-Aminopyrimidine-4-carboxylic acid is often used as a key intermediate in the preparation of complex molecules. Its presence allows for the introduction of functional groups at specific positions, facilitating the formation of desired products with high yields and selectivity. Additionally, this compound can undergo various transformations, such as acylation, alkylation, and cyclization reactions, leading to the generation of diverse molecular structures.Furthermore, the versatile nature of 2-Aminopyrimidine-4-carboxylic acid enables chemists to access a wide range of chemical derivatives with altered properties and functionalities. By strategically incorporating this compound into synthetic routes, researchers can access novel compounds with potential applications in drug discovery, materials science, and other fields.Overall, 2-Aminopyrimidine-4-carboxylic acid serves as a valuable tool in chemical synthesis, allowing for the efficient and strategic construction of complex molecules with tailored properties and functionalities. Its versatility and reactivity make it an indispensable component in the development of innovative products and materials.