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Methanone, (2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)-

HCID 81876
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Basic information

CAS
7392-62-3
Standard SMILES
COc1ccc(C(=O)c2ccc(O)cc2O)c(O)c1
InChIKey
YLQYOUPUVFQNLO-UHFFFAOYSA-N
Molecular formula
C14H12O5
Average molar mass
260.24 g/mol
Monoisotopic mass
260.06847348

Names & identifiers

Preferred name
Methanone, (2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)-
IUPAC
(2,4-dihydroxyphenyl)-(2-hydroxy-4-methoxyphenyl)methanone
English name
2,2',4-trihydroxy-4'-methoxybenzophenone
Molecular formula
C14H12O5
Molecular weight
260.24208

Names & synonyms

7392-62-3Methanone, (2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)-EINECS 230-984-9DTXSID7064657RefChem:811624DTXCID90475982,2',4-Trihydroxy-4'-methoxybenzophenone(2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)methanoneZMM9GH7Y2KSCHEMBL93206SCHEMBL30900821NS00037575
Show more names
2,4-Dihydroxyphenyl(2-hydroxy-4-methoxyphenyl) ketone

Database identifiers

CAS
7392-62-3
PubChem CID
81876
DTXSID
DTXSID7064657
UNII
ZMM9GH7Y2K
EC Number
230-984-9
Nikkaji
J278.806C

Properties

Computed structural properties

XLogP
2.9
Topological polar surface area
87 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
5
Rotatable bonds
3
Heavy atoms
19
Formal charge
0
Complexity
319

Physicochemical properties

Melting point
101 · 101-102°C
EPA Substance Registry System
Methanone, (2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)- (7392-62-3)
TSCA
TSCA listed

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Hazard information

Regulatory InformationChemical: Methanone, (2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)-
Other Safety InformationEvaluation - Chemicals not considered for in depth evaluation - Not commercially active in Australia

Safety data

tsca
TSCA listed

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationMethanone, (2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)-: INACTIVE

Preparation methods

Preparationobtained by action of 2-hydroxy-4-methoxybenzoic acid with resorcinol in the presence of zinc chloride and phos-phorous oxychloride at 6065° for 3 h (30%).

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