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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)-

1,2,4-Oxadiazol-3-amine, 5-(1,1-dimethylethyl)-

CC(c1onc(n1)N)(C)C Request for Quotation
Chemical Name: 1,2,4-Oxadiazol-3-amine, 5-(1,1-dimethylethyl)-
CAS Number: 91362-43-5
Product Number: AG00IGMD(AGN-PC-00LS1Z)
Synonyms:
MDL No:
Molecular Formula: C6H11N3O
Molecular Weight: 141.1710

Identification/Properties

Computed Properties
Molecular Weight:
141.174g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
141.09g/mol
Monoisotopic Mass:
141.09g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
10
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-tert-Butyl-1,2,4-oxadiazol-3-amine is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various organic compounds and pharmaceuticals. In chemical synthesis, 5-tert-Butyl-1,2,4-oxadiazol-3-amine is commonly employed as a key intermediate in the synthesis of heterocyclic compounds and functionalized molecules. Its presence enables the introduction of the tert-butyl functional group, enhancing the stability and altering the physicochemical properties of the resulting products. Additionally, the oxadiazole ring moiety provides a structural scaffold that can be further diversified through various chemical transformations, leading to the development of new materials and bioactive compounds with potential applications in medicinal chemistry and materials science.