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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-1,2,4-Triazole, 1-phenyl-

c1ccc(cc1)n1cncn1 Request for Quotation
Chemical Name: 1H-1,2,4-Triazole, 1-phenyl-
CAS Number: 13423-60-4
Product Number: AG003ELO(AGN-PC-0JLUJ0)
Synonyms:
MDL No:
Molecular Formula: C8H7N3
Molecular Weight: 145.1613

Identification/Properties

Properties
MP:
47℃
BP:
292.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
145.165g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
145.064g/mol
Monoisotopic Mass:
145.064g/mol
Topological Polar Surface Area:
30.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
121
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Phenyl-1H-1,2,4-triazole is a versatile compound widely utilized in chemical synthesis as a key building block in the creation of various organic molecules. This compound serves as a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and dyes due to its unique structural properties and reactivity. In chemical synthesis, 1-Phenyl-1H-1,2,4-triazole can be employed as a precursor in the formation of heterocyclic compounds, which are essential components in the development of new materials and bioactive compounds. Its ability to participate in diverse reactions, such as cycloadditions and nucleophilic substitutions, makes it a crucial tool for organic chemists in designing novel molecules with specific properties and functions. Additionally, the presence of the phenyl group in 1-Phenyl-1H-1,2,4-triazole offers opportunities for further functionalization, facilitating the creation of a wide range of chemical structures tailored to specific applications. By incorporating 1-Phenyl-1H-1,2,4-triazole into synthetic pathways, researchers can access a multitude of compounds with varying biological activities and industrial uses.