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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)-

1H-1,2,3-Triazole-4-carboxamide, 5-amino-1-phenyl-

NC(=O)c1nnn(c1N)c1ccccc1 Request for Quotation
Chemical Name: 1H-1,2,3-Triazole-4-carboxamide, 5-amino-1-phenyl-
CAS Number: 20317-25-3
Product Number: AG017C4U(AGN-PC-0JNRH0)
Synonyms:
MDL No:
Molecular Formula: C9H9N5O
Molecular Weight: 203.2007

Identification/Properties

Computed Properties
Molecular Weight:
203.205g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
203.081g/mol
Monoisotopic Mass:
203.081g/mol
Topological Polar Surface Area:
99.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
241
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

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Chemical Structure


5-Amino-1-phenyl-1H-1,2,3-triazole-4-carboxamide is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This compound serves as a valuable building block in the preparation of a variety of bioactive molecules and pharmaceuticals. Its ability to undergo various chemical transformations, such as derivatization and functional group interconversion, makes it a key component in the construction of complex organic compounds. Additionally, 5-Amino-1-phenyl-1H-1,2,3-triazole-4-carboxamide exhibits reactivity towards a range of reagents, facilitating its use in the development of novel chemical entities with potential applications in drug discovery and material science. Its strategic placement of functional groups allows for precise modifications that can influence the physicochemical properties and biological activities of the final products. This compound's role in chemical synthesis extends beyond basic reactions, making it an indispensable tool for synthetic chemists seeking to access diverse molecular architectures with enhanced properties and functionalities.