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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)-

1-Propanone, 1-[2-(oxiranylmethoxy)phenyl]-3-phenyl-

O=C(c1ccccc1OCC1CO1)CCc1ccccc1 Request for Quotation
Chemical Name: 1-Propanone, 1-[2-(oxiranylmethoxy)phenyl]-3-phenyl-
CAS Number: 22525-95-7
Product Number: AG00I4G3(AGN-PC-05XGHL)
Synonyms:
MDL No:
Molecular Formula: C18H18O3
Molecular Weight: 282.3337

Identification/Properties

Properties
MP:
56-58 °C
BP:
452.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
282.339g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
282.126g/mol
Monoisotopic Mass:
282.126g/mol
Topological Polar Surface Area:
38.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
335
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
P261-P280-P305+P351+P338-P304+P340
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2-(2,3-Epoxypropoxy)phenyl)-3-phenyl-1-propanone is a versatile compound widely used in chemical synthesis for its unique structural features and reactivity. It serves as a crucial building block in the preparation of various organic compounds, particularly in the field of organic chemistry and pharmaceutical research. This compound is commonly employed as a key intermediate in the synthesis of complex molecules and functional materials due to its ability to undergo diverse chemical transformations.One of the prominent applications of 1-(2-(2,3-Epoxypropoxy)phenyl)-3-phenyl-1-propanone is its role as a precursor in the preparation of biologically active substances, such as pharmaceutical drugs and agrochemicals. Its distinct chemical structure allows for the selective modification of functional groups, enabling the synthesis of compounds with specific biological activities. Additionally, this compound can participate in various reactions, including nucleophilic addition, condensation, and oxidation, making it a valuable tool in the development of new chemical entities.Moreover, 1-(2-(2,3-Epoxypropoxy)phenyl)-3-phenyl-1-propanone finds application in the field of material science for the synthesis of polymers, coatings, and specialty chemicals. Its epoxy and carbonyl functional groups provide opportunities for crosslinking, polymerization, and surface modification, leading to the creation of advanced materials with tailored properties. By incorporating this compound into polymer matrices, researchers can enhance the mechanical strength, thermal stability, and chemical resistance of the resulting materials.Overall, the use of 1-(2-(2,3-Epoxypropoxy)phenyl)-3-phenyl-1-propanone in chemical synthesis offers a wide range of possibilities for designing and synthesizing novel compounds with desired functionalities and properties. Its versatility and reactivity make it a valuable asset in the hands of chemists and researchers striving to develop innovative solutions in various scientific disciplines.