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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-phenyl-

OCc1onc(c1)c1ccccc1 Request for Quotation
Chemical Name: 5-Isoxazolemethanol, 3-phenyl-
CAS Number: 90924-12-2
Product Number: AG006GFD(AGN-PC-0KKPIJ)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2
Molecular Weight: 175.1840

Identification/Properties

Properties
MP:
45-47 °C
BP:
362.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
175.187g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
175.063g/mol
Monoisotopic Mass:
175.063g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
157
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Phenyl-5-isoxazolyl)methanol is a versatile compound commonly used in chemical synthesis as a key building block for the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows for efficient functionalization and derivatization, making it a valuable tool in the creation of complex molecular structures.In organic synthesis, (3-Phenyl-5-isoxazolyl)methanol serves as a valuable starting material for the construction of heterocyclic compounds through various reactions such as cyclization, oxidation, and reduction. Its isoxazole ring provides opportunities for further modification, enabling the synthesis of diverse molecules with potential bioactivity and therapeutic properties.Additionally, (3-Phenyl-5-isoxazolyl)methanol can be utilized in the preparation of chiral intermediates and ligands for asymmetric synthesis, contributing to the development of new methodologies for enantioselective transformations. Its presence in the chemical toolbox of a synthetic chemist opens up avenues for innovative strategies in drug discovery, material science, and chemical manufacturing.