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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)-

Methanone, [2-hydroxy-4-(2-propenyloxy)phenyl]phenyl-

C=CCOc1ccc(c(c1)O)C(=O)c1ccccc1 Request for Quotation
Chemical Name: Methanone, [2-hydroxy-4-(2-propenyloxy)phenyl]phenyl-
CAS Number: 2549-87-3
Product Number: AG003KN7(AGN-PC-0JLPIY)
Synonyms:
MDL No:
Molecular Formula: C16H14O3
Molecular Weight: 254.2806

Identification/Properties

Properties
MP:
67-70 °C(lit.);
BP:
403 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
254.285g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
254.094g/mol
Monoisotopic Mass:
254.094g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
307
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Allyloxy)-2-hydroxybenzophenone, also known as benzophenone-2-allyl ether, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic synthesis, this compound serves as a valuable building block for creating various functionalized molecules and polymers. Due to the presence of both an allyl group and a hydroxybenzophenone moiety, it can participate in a range of chemical reactions to introduce new functional groups or modify existing ones.One of the key applications of 4-(Allyloxy)-2-hydroxybenzophenone is as a photoinitiator in the formulation of UV-curable materials. When exposed to UV radiation, this compound undergoes photolysis to generate free radicals, initiating polymerization reactions in systems such as inks, coatings, adhesives, and sealants. This property makes it an essential component in the production of UV-curable polymers with tailored properties and performance characteristics.Furthermore, 4-(Allyloxy)-2-hydroxybenzophenone can also be utilized in the synthesis of advanced materials, such as liquid crystals and functionalized nanoparticles, by serving as a reactive intermediate or a chemical modifier. Its ability to act as a crosslinking agent or a coupling reagent enables the design and fabrication of novel materials with specific functionalities and applications in various industries, including electronics, pharmaceuticals, and biomedical engineering.