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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)-

5-(methoxymethyl)-1,2,4-oxadiazol-3-amine(SALTDATA

COCc1nc(no1)N Request for Quotation
Chemical Name: 5-(methoxymethyl)-1,2,4-oxadiazol-3-amine(SALTDATA
CAS Number: 1243250-15-8
Product Number: AG009DXB(AGN-PC-0WB5RQ)
Synonyms:
MDL No: MFCD17078854
Molecular Formula: C4H7N3O2
Molecular Weight: 129.1173

Identification/Properties

Computed Properties
Molecular Weight:
129.119g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
129.054g/mol
Monoisotopic Mass:
129.054g/mol
Topological Polar Surface Area:
74.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
89.9
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Methoxymethyl)-1,2,4-oxadiazol-3-amine, commonly referred to as $name$, serves as a valuable building block in chemical synthesis. This compound is utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structural features make it a versatile reagent for the introduction of functional groups, enabling the synthesis of diverse molecular architectures. In addition, 5-(Methoxymethyl)-1,2,4-oxadiazol-3-amine exhibits excellent reactivity towards a variety of coupling reactions, allowing for the efficient construction of complex molecules with high yield and selectivity. Its consistent performance and compatibility with a wide range of synthetic protocols make it an indispensable tool for synthetic chemists seeking to streamline their processes and access novel chemical entities.