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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-Isoxazolemethanol, 3-(phenylmethoxy)-

OCc1onc(c1)OCc1ccccc1 Request for Quotation
Chemical Name: 5-Isoxazolemethanol, 3-(phenylmethoxy)-
CAS Number: 123320-44-5
Product Number: AG000KCF(AGN-PC-0LQ19O)
Synonyms:
MDL No:
Molecular Formula: C11H11NO3
Molecular Weight: 205.2099

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
205.213g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
205.074g/mol
Monoisotopic Mass:
205.074g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
183
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

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Chemical Structure


The versatile compound (3-(Benzyloxy)isoxazol-5-yl)methanol serves as a valuable building block in chemical synthesis, particularly in the creation of complex organic molecules. Its strategic placement of functional groups enables efficient modifications and derivatizations, making it a key component in the development of pharmaceuticals, agrochemicals, and advanced materials. By leveraging the unique reactivity and selectivity of this compound, chemists can streamline synthetic routes and access diverse molecular scaffolds with enhanced structural and stereochemical diversity.