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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)-

Isoxazole, 3-methyl-5-phenyl-

Cc1noc(c1)c1ccccc1 Request for Quotation
Chemical Name: Isoxazole, 3-methyl-5-phenyl-
CAS Number: 1008-75-9
Product Number: AG0002XC(AGN-PC-0JMP3I)
Synonyms:
MDL No:
Molecular Formula: C10H9NO
Molecular Weight: 159.1846

Identification/Properties

Computed Properties
Molecular Weight:
159.188g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
159.068g/mol
Monoisotopic Mass:
159.068g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
143
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methyl-5-phenylisoxazole, a unique heterocyclic compound, finds crucial application in chemical synthesis due to its versatile reactivity and structural properties. In the realm of organic chemistry, this molecule serves as a valuable building block for the synthesis of various functionalized compounds. By harnessing the reactivity of the isoxazole ring and the substituents at positions 3 and 5, chemists can efficiently introduce diverse functional groups to generate novel molecules with tailored properties. Additionally, 3-Methyl-5-phenylisoxazole plays a significant role in the development of pharmaceuticals, agrochemicals, and materials with applications in medicinal chemistry, crop protection, and materials science. Its structural uniqueness and synthetic utility make it a valuable tool for chemists striving to advance the frontiers of chemical innovation.