Información del producto
- 1,1-Bis(4-hydroxyphenyl)-1-phenylethane-13C6
- 1-Phenyl-1,1-bis(4-hydroxyphenyl)ethane-13C6
- 4,4'-(1-Phenylethylidene)bisphenol-13C6
- 4,4'-(1-Phenylethylidene)diphenol-13C6
- 4,4'-(a-Methylbenzylidene)diphenol-13C6
- Bis(4-hydroxyphenyl)methylphenylmethane-13C6
- Bisp-Ap-13C6
- Bisphenol ACP-13C6
- NK-AP-13C6
- a,a-Bis(4-hydroxyphenyl)ethylbenzene-13C6
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- 1,1-Bis(4-hydroxyphenyl)-1-phenylethane
- 1-Phenyl-1,1-bis(4-hydroxyphenyl)ethane
- 4,4'-(1-Phenylethane-1,1-Diyl)Diphenol
- 4,4'-(1-Phenylethylidene) Biphenol
- 4,4-(1-alpha-Methylbenzylidene)bisphenol
- 4,4′-(1-Phenylethylidene)bis[phenol]
- 4,4′-(1-Phenylethylidene)diphenol
- 4,4′-(α-Methylbenzylidene)diphenol
- Bis(4-hydroxyphenyl)methylphenylmethane
- Bisp-Ap
- Bisphenol ACP
- Bisphenol AP
- Nk-Ap
- Phenol, 4,4′-(1-phenylethylidene)bis-
- Phenol, 4,4′-(α-methylbenzylidene)di-
- α,α-Bis(4-hydroxyphenyl)ethylbenzene
Applications Bisphenol AP-13C6 is the isotope labelled analog of Bisphenol AP. Bisphenol AP is used to prepare triphenylmethane derivatives as inhibitors of hepatitis C virus helicase. It is a derivative of Bisphenol A (B519495) which is a monomer used for policarbonate and epoxy resins.
References Chen, C., et al.: J. Med. Chem., 52, 2716 (2009); Krishnan, A.V., et al.: Endocrinology, 132, 2279 (1993); Steinmetz, R., et al.: Trends Endocrinol. Metab., 9, 124 (1998); Petersen, H., et al.: Eur. Food Res. Technol., 216, 355 (2003)
Propiedades químicas
Consulta técnica sobre: TR-B519487 Bisphenol AP-13C6
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