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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, (4-hydroxyphenyl)(4-methylphenyl)-

Cc1ccc(cc1)C(=O)c1ccc(cc1)O Request for Quotation
Chemical Name: Methanone, (4-hydroxyphenyl)(4-methylphenyl)-
CAS Number: 134-92-9
Product Number: AG003LIC(AGN-PC-0JL7PA)
Synonyms:
MDL No:
Molecular Formula: C14H12O2
Molecular Weight: 212.2439

Identification/Properties

Computed Properties
Molecular Weight:
212.248g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
212.084g/mol
Monoisotopic Mass:
212.084g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
233
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-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Hydroxy-4'-methylbenzophenone, also known as p-methylbenzophenone-4 or 4-Methylbenzophenone-4-ol, is a key chemical compound widely utilized in chemical synthesis and various industries. This compound serves as a versatile building block in the creation of UV-curable coatings, adhesives, and polymers. Its photoinitiating properties make it an essential component in the formulation of sunscreens, as it effectively absorbs and dissipates harmful UV radiation, providing photoprotection for the skin. In addition, 4-Hydroxy-4'-methylbenzophenone is commonly employed in the synthesis of specialty chemicals, pharmaceuticals, and fragrances due to its unique molecular structure and reactivity. Its capability to undergo various chemical reactions makes it a valuable intermediate in the production of complex organic compounds with diverse applications in the chemical industry.