553476
Bisphenol C
98%
Synonym(s):
Bis(4-hydroxyphenyl)-2,2-dichloroethylene
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About This Item
Linear Formula:
Cl2C=C(C6H4OH)2
CAS Number:
Molecular Weight:
281.13
EC Number:
238-940-0
UNSPSC Code:
12162002
PubChem Substance ID:
Beilstein/REAXYS Number:
2052978
MDL number:
InChI key
OWEYKIWAZBBXJK-UHFFFAOYSA-N
InChI
1S/C14H10Cl2O2/c15-14(16)13(9-1-5-11(17)6-2-9)10-3-7-12(18)8-4-10/h1-8,17-18H
SMILES string
Oc1ccc(cc1)\C(=C(/Cl)Cl)c2ccc(O)cc2
assay
98%
mp
213-217 °C (lit.)
Application
Used in the preparation of flame-resistant polycarbonates; Modifier to form thermosets with improved flame resistant.
Regulatory Information
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Justin M Conley et al.
Toxicological sciences : an official journal of the Society of Toxicology, 153(2), 382-395 (2016-07-31)
In vitro estrogen receptor assays are valuable tools for identifying environmental samples and chemicals that display estrogenic activity. However, in vitro potency cannot necessarily be extrapolated to estimates of in vivo potency because in vitro assays are currently unable to
Vanessa Delfosse et al.
Environmental health perspectives, 122(12), 1306-1313 (2014-09-27)
Individuals are exposed daily to environmental pollutants that may act as endocrine-disrupting chemicals (EDCs), causing a range of developmental, reproductive, metabolic, or neoplastic diseases. With their mostly hydrophobic pocket that serves as a docking site for endogenous and exogenous ligands
Caroline Pinto et al.
Toxicology and applied pharmacology, 380, 114709-114709 (2019-08-16)
The high volume production compound bisphenol A (BPA) is of environmental concern largely because of its estrogenic activity. Consequently, BPA analogues have been synthesized to be considered as replacement molecules for BPA. These analogues need to be thoroughly evaluated for
Xiaohui Liu et al.
Toxicology and applied pharmacology, 377, 114610-114610 (2019-06-14)
An endocrine-disrupting chemical Bisphenol A (BPA) binds specifically to a nuclear receptor (NR) named ERRγ. Although the importance of receptor-binding evaluation for human NRs is often stressed, the binding characteristics of so-called next-generation (NextGen) bisphenol compounds are still poorly understood.
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