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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)-

Benzaldehyde, 4-(1H-1,2,3-triazol-1-yl)-

O=Cc1ccc(cc1)n1ccnn1 Request for Quotation
Chemical Name: Benzaldehyde, 4-(1H-1,2,3-triazol-1-yl)-
CAS Number: 41498-10-6
Product Number: AG0071UW(AGN-PC-0NBJ2H)
Synonyms:
MDL No:
Molecular Formula: C9H7N3O
Molecular Weight: 173.1714

Identification/Properties

Computed Properties
Molecular Weight:
173.175g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
173.059g/mol
Monoisotopic Mass:
173.059g/mol
Topological Polar Surface Area:
47.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
178
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(1H-1,2,3-Triazol-1-yl)benzaldehyde is a versatile compound commonly utilized in chemical synthesis as a key building block in the creation of various organic compounds. Due to its unique structure containing a triazole ring, this aldehyde offers opportunities for the development of novel molecules with desirable properties.One significant application of 4-(1H-1,2,3-Triazol-1-yl)benzaldehyde is in the synthesis of pharmaceuticals and agrochemicals. Its triazole moiety can serve as a pharmacophore, enabling the design and production of bioactive compounds with potential therapeutic or pesticidal effects. Additionally, the aldehyde group in this molecule allows for further functionalization, facilitating the modification of its chemical properties to optimize its biological activity.Furthermore, 4-(1H-1,2,3-Triazol-1-yl)benzaldehyde can be employed in the preparation of fluorescent probes and dyes. By incorporating this compound into fluorescent molecules, researchers can develop tools for cellular imaging, drug delivery systems, and molecular labeling techniques. The triazole ring enhances the fluorescence properties of these compounds, making them valuable in various biological and chemical applications.In summary, the strategic utilization of 4-(1H-1,2,3-Triazol-1-yl)benzaldehyde in chemical synthesis allows for the construction of diverse compounds with potential pharmaceutical, agrochemical, and fluorescent properties. Its structural features make it a valuable building block for the development of innovative materials and bioactive molecules.