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Details

Stereochemistry ACHIRAL
Molecular Formula C23H24O4
Molecular Weight 364.4343
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4,4'-ISOPROPYLIDENEDIPHENOL DIMETHACRYLATE

SMILES

CC(=C)C(=O)OC1=CC=C(C=C1)C(C)(C)C2=CC=C(OC(=O)C(C)=C)C=C2

InChI

InChIKey=QUZSUMLPWDHKCJ-UHFFFAOYSA-N
InChI=1S/C23H24O4/c1-15(2)21(24)26-19-11-7-17(8-12-19)23(5,6)18-9-13-20(14-10-18)27-22(25)16(3)4/h7-14H,1,3H2,2,4-6H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Rational quantitative structure-activity relationship (RQSAR) screen for PXR and CAR isoform-specific nuclear receptor ligands.
2010-12-05
Fast preparation of photopolymerized poly(benzyl methacrylate-co-bisphenol A dimethacrylate) monoliths for capillary electrochromatography.
2010-05-28
Effect of Energy Density on the Physical Properties of Resin-Based Restorative Materials when Polymerized with Quartz-Tungsten Halogen or LED-Light.
2010-04
Molecular toxicology of substances released from resin-based dental restorative materials.
2009-09-04
Contact allergy to epoxy (meth)acrylates.
2009-07
Selective removal of bisphenol A from serum using molecular imprinted polymer membranes.
2009-02
Effect of adhesive hydrophilicity and curing time on the permeability of resins bonded to water vs. ethanol-saturated acid-etched dentin.
2009-01
Polymer induced crystal organization of composite resins.
2008-12
Experimental composites made of electron beam irradiated reinforced fillers.
2008-05
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Endocrine-disrupting potential of bisphenol A, bisphenol A dimethacrylate, 4-n-nonylphenol, and 4-n-octylphenol in vitro: new data and a brief review.
2007-12
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Alterations in steroid hormone production by porcine ovarian granulosa cells caused by bisphenol A and bisphenol A dimethacrylate.
2005-12-01
Induction of cyclooxygenase-2 mRNA and protein expression by dentin bonding agents in human gingival fibroblasts.
2004-08-15
Reproductive toxic effect of bisphenol A dimethacrylate in mice.
2004-06-15
Synthetic polymers adsorbing bisphenol A and its analogues prepared by covalent molecular imprinting using bisphenol A dimethacrylate as a template molecule.
2004-04
Stability of bisphenol A, triethylene-glycol dimethacrylate, and bisphenol A dimethacrylate in whole saliva.
2002-03
Aromatic dental monomers affect the activity of cholesterol esterase.
2001-11-26
Heterogeneous distribution of single-bottle adhesive monomers in the resin-dentin interdiffusion zone.
2001-07
Estrogenicity of fissure sealants and adhesive resins determined by reporter gene assay.
2001-06
Estrogenicity of fissure sealants and adhesive resins determined by reporter gene assay.
2000-11
The estrogenicity of bisphenol A-related diphenylalkanes with various substituents at the central carbon and the hydroxy groups.
1998-03
Estrogenicity of resin-based composites and sealants used in dentistry.
1996-03
Name Type Language
2-PROPENOIC ACID, 2-METHYL-, (1-METHYLETHYLIDENE)DI-4,1-PHENYLENE ESTER
Preferred Name English
4,4'-ISOPROPYLIDENEDIPHENOL DIMETHACRYLATE
Systematic Name English
DIPHENYLOLPROPANE DIMETHACRYLATE
Common Name English
2,2-PROPANEDIYLDI-4,1-PHENYLENE BIS(2-METHYLACRYLATE)
Systematic Name English
PROPANE-2,2-DIYLDIBENZENE-4,1-DIYL BIS(2-METHYLPROP-2-ENOATE)
Systematic Name English
BISPHENOL A DIMETHACRYLATE
Systematic Name English
PROPANE-2,2-DIYLDI-4,1-PHENYLENE BIS(2-METHYLACRYLATE)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID80863135
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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CAS
3253-39-2
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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MESH
C002462
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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CHEBI
34579
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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ECHA (EC/EINECS)
221-846-9
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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PUBCHEM
76739
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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FDA UNII
982O8255NE
Created by admin on Mon Mar 31 20:37:21 GMT 2025 , Edited by admin on Mon Mar 31 20:37:21 GMT 2025
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