CAS 1470-79-7: 2,4,4'-Trihydroxybenzophenone
Formula:C13H10O4
InChI:InChI=1S/C13H10O4/c14-9-3-1-8(2-4-9)13(17)11-6-5-10(15)7-12(11)16/h1-7,14-16H
InChI key:InChIKey=OKJFKPFBSPZTAH-UHFFFAOYSA-N
SMILES:C(=O)(C1=C(O)C=C(O)C=C1)C2=CC=C(O)C=C2
Synonyms:- (2,4-Dihydroxyphenyl)(4-Hydroxyphenyl)Methanone
- 2,4-Dihydroxyphenyl p-hydroxybenzyl ketone
- Benzophenone, 2,4,4′-trihydroxy-
- Methanone, (2,4-dihydroxyphenyl)(4-hydroxyphenyl)-
- NSC 76052
- 2,4,4-Trihydroxybenzophenone
- 2,4,4′-Trihydroxybenzophenone
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Found 5 products.
2,4,4'-Trihydroxybenzophenone
CAS:Formula:C13H10O4Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:230.222,4,4'-Trihydroxybenzophenone
CAS:2,4,4'-Trihydroxybenzophenone is a synthetic compound that has been shown to have receptor binding properties. It also inhibits the effects of estradiol by competitively binding to the estrogen receptors α and β in the presence of estradiol. 2,4,4'-Trihydroxybenzophenone has been found to exert a variety of health effects including carcinogenic and genotoxic effects. These effects are mediated through its ability to bind with DNA and affect the expression of genes. The uv irradiation can cause the formation of reactive oxygen species in cells which can lead to DNA damage. 2,4,4'-Trihydroxybenzophenone also has an estrogenic effect on human breast cancer cells in vitro as well as estrogen-dependent mammary tumors in rats. This agent binds with high affinity to estrogen receptors α and β.Formula:C13H10O4Purity:Min. 95%Color and Shape:White To Light (Or Pale) Yellow SolidMolecular weight:230.22 g/molRef: 3D-FT30132
Discontinued product(2,4-Dihydroxyphenyl)(4-hydroxyphenyl)methanone
CAS:(2,4-Dihydroxyphenyl)(4-hydroxyphenyl)methanonePurity:98+%Molecular weight:230.22g/molMethanone, (2,4-dihydroxyphenyl)(4-hydroxyphenyl)-
CAS:Formula:C13H10O4Purity:98%Color and Shape:SolidMolecular weight:230.2161
