553476
双酚C
98%
别名:
2,2-双(4-羟基苯基)-1,1-二氯乙烯
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线性分子式:
Cl2C=C(C6H4OH)2
化学文摘社编号:
分子量:
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
用于制备阻燃性聚碳酸酯；用作形成更高阻燃性热固性树脂的改性剂。
法规信息
新产品
此项目有
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
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
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
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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