1. Home
  2. (5-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL

OCc1noc(n1)C1CCC1 Request for Quotation
Chemical Name: (5-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL
CAS Number: 915925-42-7
Product Number: AG00GTQ7(AGN-PC-0WB3OF)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O2
Molecular Weight: 154.1665

Identification/Properties

Computed Properties
Molecular Weight:
154.169g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
154.074g/mol
Monoisotopic Mass:
154.074g/mol
Topological Polar Surface Area:
59.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
138
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(5-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL, a powerful building block in chemical synthesis, serves as a versatile reagent in various organic transformations. This compound exhibits a unique structure that enables it to participate in diverse reactions, making it a valuable tool for synthetic chemists. Its cyclobutyl group imparts steric effects, influencing the regioselectivity and stereoselectivity of reactions it undergoes.In organic synthesis, (5-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL is commonly utilized in the preparation of heterocyclic compounds, serving as a key intermediate in the construction of complex molecular architectures. Its oxadiazole moiety plays a crucial role in enhancing the chemical and biological properties of the resulting compounds, making it a significant component in drug discovery and development processes.Moreover, the presence of a methanol functional group in this molecule enables it to participate in various transformations such as nucleophilic addition reactions, substitution reactions, and transition metal-catalyzed transformations. This versatility makes (5-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL a valuable reagent for the synthesis of pharmaceuticals, agrochemicals, and functional materials with tailored properties.In summary, the strategic incorporation of (5-CYCLOBUTYL-1,2,4-OXADIAZOL-3-YL)METHANOL in chemical synthesis enables the creation of diverse organic compounds with enhanced properties, making it an indispensable component in modern synthetic chemistry endeavors.