benzofenon

Also known as alpha -oxodiphenylmethane, benzoylbenzene, diphenyl ketone, diphenylmethanone, phenyl ketone, benzopheneone, diphenylketone, di(phenyl)methanone

związek chemiczny

In the Vinony graph

Vinony's link graph records 129 inbound references to benzofenon, and connects out to carbon tetrachloride, sunscreen and International Standard Book Number.

It is catalogued under topics including Benzophenones, Chembox having GHS data and Chembox image size set.

Vinony links it to 30 Wikipedia language editions.

Chemical data

Formula: C13H10O
Molecular weight: 182.22 g/mol
IUPAC name: diphenylmethanone
SMILES: C1=CC=C(C=C1)C(=O)C2=CC=CC=C2
InChIKey: RWCCWEUUXYIKHB-UHFFFAOYSA-N
XLogP: 3.4
Polar surface area: 17.1 Å²
H-bond donors: 0
H-bond acceptors: 1
Formal charge: 0

via PubChem

Drug data · ChEMBL

Molecule type: Small molecule

via ChEMBL · EBI

Research

13,704 papers

Safety of benzophenone-type UV filters: A mini review focusing on carcinogenicity, reproductive and developmental toxicity.Chemosphere · 2023
Benzophenone photophores in biochemistry.Biochemistry · 1994
Benzophenone photoprobes for phosphoinositides, peptides and drugs.Photochemistry and photobiology · 1997
Is the commonly used UV filter benzophenone-3 a risk factor for the nervous system?Acta biochimica Polonica · 2021
Stability and Removal of Benzophenone-Type UV Filters from Water Matrices by Advanced Oxidation Processes.Molecules (Basel, Switzerland) · 2022

via PubMed

Wikidata facts

Has part: oxygen
Mass: 182.073
Autonomy: 560

Show 11 more facts

Commons category: Benzophenone
subject has role: photosensitizer
chemical formula: C₁₃H₁₀O
canonical SMILES: C1=CC=C(C=C1)C(=O)C2=CC=CC=C2
boiling point: 305.4
melting point: 47.88
solubility: 0.14
found in taxon: soybean
described by source: Encyclopædia Britannica 11th edition
ionization energy: 9.05
different from: acetophenone

Sources (4)

via Wikidata · CC0

Article · Polski

Benzofenon (difenyloketon, keton difenylowy) – organiczny związek chemiczny, najprostszy keton aromatyczny. W małych ilościach powstaje w organizmie podczas metabolizmu niektórych benzodiazepin. Praktycznie nie rozpuszcza się w wodzie, dobrze rozpuszczalny w rozpuszczalnikach organicznych. Stosowany do wyrobu leków, kosmetyków i środków owadobójczych. Pochodne bywają stosowane w filtrach przeciwsłonecznych.

Abstract from DBpedia / Wikipedia · CC BY-SA