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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)-

Ethanone, 1-(3-phenyl-5-isoxazolyl)-

CC(=O)c1onc(c1)c1ccccc1 Request for Quotation
Chemical Name: Ethanone, 1-(3-phenyl-5-isoxazolyl)-
CAS Number: 2048-69-3
Product Number: AG0029PN(AGN-PC-0KK6ZA)
Synonyms:
MDL No:
Molecular Formula: C11H9NO2
Molecular Weight: 187.1947

Identification/Properties

Properties
MP:
107-108,5 °C
BP:
373 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
187.198g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
187.063g/mol
Monoisotopic Mass:
187.063g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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


1-(3-Phenylisoxazol-5-yl)ethanone, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This organic compound plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure containing a phenylisoxazole moiety imparts specific properties that are beneficial for designing and synthesizing complex molecules with desired biological activities.In chemical synthesis, 1-(3-Phenylisoxazol-5-yl)ethanone serves as a key building block for the construction of heterocyclic compounds and biologically active molecules. Its reactivity allows for the functionalization of the phenylisoxazole ring and the ethanone group, enabling the introduction of specific chemical groups that can modulate the compound's properties and interactions with biological targets.Furthermore, the presence of the isoxazole ring confers the compound with unique characteristics such as potential pharmacophores, which are essential for drug design and development. By incorporating 1-(3-Phenylisoxazol-5-yl)ethanone into molecular structures, chemists can explore diverse synthetic pathways to create novel compounds with enhanced bioavailability, target selectivity, and therapeutic efficacy.Overall, the application of 1-(3-Phenylisoxazol-5-yl)ethanone in chemical synthesis offers researchers an invaluable tool for the efficient and strategic assembly of structurally diverse molecules with significant potential for pharmaceutical and agrochemical applications.