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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)-

1,2,5-Oxadiazol-3-amine, 4-methyl-

Nc1nonc1C Request for Quotation
Chemical Name: 1,2,5-Oxadiazol-3-amine, 4-methyl-
CAS Number: 17647-70-0
Product Number: AG0024P2(AGN-PC-0JKK80)
Synonyms:
MDL No:
Molecular Formula: C3H5N3O
Molecular Weight: 99.0913

Identification/Properties

Computed Properties
Molecular Weight:
99.093g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
99.043g/mol
Monoisotopic Mass:
99.043g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
67.2
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:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyl-1,2,5-oxadiazol-3-amine, also known as $name$, serves as a valuable building block in chemical synthesis due to its versatile reactivity and functional groups. This compound finds application in the development and preparation of various organic compounds and materials.In the realm of chemical synthesis, 4-Methyl-1,2,5-oxadiazol-3-amine plays a crucial role as a key intermediate in the synthesis of heterocyclic compounds. Its unique structure containing an oxadiazole ring facilitates the formation of diverse derivatives through functionalization reactions. This compound can undergo substitution, reduction, or addition reactions to introduce different substituents or functional groups, allowing for the modification and customization of the final product.Furthermore, 4-Methyl-1,2,5-oxadiazol-3-amine is utilized in the development of pharmaceuticals, agrochemicals, and materials science. By incorporating this compound into molecular structures, chemists can access new compounds with varied properties and applications. Its presence in the chemical synthesis process enables the creation of novel molecules with enhanced biological activity, improved performance, or tailored functionalities for specific industrial applications.