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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(1H)-Pyridinone, 3,4-diamino-

Nc1c(N)ccnc1O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 3,4-diamino-
CAS Number: 33631-02-6
Product Number: AG00C70J(AGN-PC-042YIN)
Synonyms:
MDL No:
Molecular Formula: C5H7N3O
Molecular Weight: 125.1286

Identification/Properties

Properties
BP:
545.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
125.131g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
125.059g/mol
Monoisotopic Mass:
125.059g/mol
Topological Polar Surface Area:
81.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
204
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#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,4-Diaminopyridin-2-ol is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its primary application lies in the development of novel drug candidates and active pharmaceutical ingredients (APIs).In chemical synthesis, 3,4-Diaminopyridin-2-ol can be used as a precursor for the synthesis of heterocyclic compounds with potent biological activities. By incorporating this compound into the molecular structure, researchers can modulate the pharmacological properties of the final products, such as enhanced bioavailability, improved metabolic stability, and targeted drug delivery.Furthermore, 3,4-Diaminopyridin-2-ol plays a crucial role in the development of catalysts and ligands for various organic transformations. Its ability to coordinate with metal ions allows for the design of efficient catalyst systems for organic reactions, including cross-coupling reactions, asymmetric transformations, and C-H functionalization.Overall, the application of 3,4-Diaminopyridin-2-ol in chemical synthesis demonstrates its significance in the discovery and development of new chemical entities with potential therapeutic benefits and industrial applications.