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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)-

3-Pyridinecarboxamide, 6-amino-

Nc1ccc(cn1)C(=O)N Request for Quotation
Chemical Name: 3-Pyridinecarboxamide, 6-amino-
CAS Number: 329-89-5
Product Number: AG003N2V(AGN-PC-0JK934)
Synonyms:
MDL No:
Molecular Formula: C6H7N3O
Molecular Weight: 137.1393

Identification/Properties

Properties
MP:
245-248 °C(lit.)
BP:
381.6°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.6910 (estimate)
Computed Properties
Molecular Weight:
137.142g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
137.059g/mol
Monoisotopic Mass:
137.059g/mol
Topological Polar Surface Area:
82A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
137
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Aminonicotinamide is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organic chemistry. This molecule serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its unique structural properties, 6-Aminonicotinamide can participate in a variety of chemical reactions to form important intermediates and final products with enhanced biological activities.One key application of 6-Aminonicotinamide in chemical synthesis is its use as a precursor in the preparation of heterocyclic compounds, such as pyridine derivatives. These compounds are essential in the development of drugs, dyes, and materials with diverse functionalities. 6-Aminonicotinamide can undergo various synthetic transformations, including condensation, reduction, and substitution reactions, to yield valuable derivatives that contain the characteristic pyridine ring.Furthermore, 6-Aminonicotinamide plays a crucial role in the synthesis of bioactive molecules, such as enzyme inhibitors and antitumor agents. By selectively modifying the amino and pyridine moieties of 6-Aminonicotinamide, chemists can design novel compounds with improved biological properties and reduced side effects. This compound's versatility and reactivity make it a valuable tool for medicinal chemists and researchers striving to develop new therapeutic agents with enhanced efficacy.In conclusion, the use of 6-Aminonicotinamide in chemical synthesis enables the efficient construction of complex molecules with diverse applications in drug discovery and material science. Its role as a key intermediate in the synthesis of biologically active compounds highlights its importance in advancing the field of organic chemistry.