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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,3-(5-methyl-1,2,4-oxadiazol-3-yl)-

O=Cc1cccc(c1)c1noc(n1)C Request for Quotation
Chemical Name: Benzaldehyde,3-(5-methyl-1,2,4-oxadiazol-3-yl)-
CAS Number: 852180-68-8
Product Number: AG004VYG(AGN-PC-0UYWO2)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O2
Molecular Weight: 188.1827

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
188.186g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
188.059g/mol
Monoisotopic Mass:
188.059g/mol
Topological Polar Surface Area:
56A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
210
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-H319
Precautionary Statements:
P264-P270-P280-P301+P312+P330-P305+P351+P338-P337+P313-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzaldehyde, commonly referred to as $name$, is a versatile chemical compound that finds extensive application in various chemical synthesis processes. Its unique molecular structure, consisting of a benzaldehyde moiety attached to a 1,2,4-oxadiazole ring with a methyl group at the 5-position, imparts specific reactivity and functionality ideal for several synthetic pathways.In organic chemistry, $name$ serves as a valuable building block for the synthesis of diverse compounds due to its aromatic aldehyde group, which can participate in numerous reactions like condensations, nucleophilic additions, and redox transformations. The presence of the oxadiazole ring introduces heteroatom functionality, expanding the scope of potential reactions and applications.One key application of 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzaldehyde lies in the synthesis of pharmaceutical intermediates and bioactive molecules. The unique structure of $name$ can be utilized to introduce specific pharmacophores or functional groups into drug candidates, enhancing their biological activity or target specificity.Furthermore, $name$ can be employed in material science for the preparation of advanced polymers, dyes, and organic electronic components. Its judicious incorporation into polymer chains or conjugated systems can influence the physical, optical, or electronic properties of the resulting materials, offering tailored solutions for various applications.In summary, the strategic use of 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzaldehyde in chemical synthesis enables the construction of complex molecules with defined structures and properties, making it a valuable reagent in the hands of synthetic chemists and researchers across different disciplines.