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Sigma-Aldrich P28263 2-Phenylphenol 99% CAS No.: 90-43-7 2 kg
Brand
Stock Code
LB.SA.P28263-2KG
Kısa Bilgi
Synonym(s): 2-Hydroxybiphenyl Linear Formula: C6H5C6H4OH CAS Number: 90-43-7 Molecular Weight: 170.21 Beilstein: 606907 EC Number: 201-993-5 MDL number: MFCD00002208 UNSPSC Code: 12352100 PubChem Substance ID: 24898365 NACRES: NA.22
| Sigma-Aldrich P28263 2-Phenylphenol 99% CAS No.: 90-43-7 2 kg |
| Synonym(s): 2-Hydroxybiphenyl Linear Formula: C6H5C6H4OH CAS Number: 90-43-7 Molecular Weight: 170.21 Beilstein: 606907 EC Number: 201-993-5 MDL number: MFCD00002208 UNSPSC Code: 12352100 PubChem Substance ID: 24898365 NACRES: NA.22 |
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PROPERTIES
vapor pressure 7 mmHg ( 140 °C)
Quality Level 200 Assay 99% form solid bp 282 °C (lit.) mp 57-59 °C (lit.) fluorescence λex 231 nm; λem 356 nm SMILES string Oc1ccccc1-c2ccccc2 InChI 1S/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13H InChI key LLEMOWNGBBNAJR-UHFFFAOYSA-N DESCRIPTION General description 2-Phenylphenol, also known as o-phenylphenol, is commonly used as a chemical intermediate for the synthesis of pharmaceuticals, dyes, and fragrances.[1][2][3] Application 2-Phenylphenol can be used as a precursor in the synthesis of: - Dibenzofurans via palladium-catalyzed, phenol-directed C-H activation/C-O cyclization[4] or copper-catalyzed aerobic C-H activation, followed by cycloetherification.[5] - 6H-Dibenzo[b,d]pyran-6-ones via ruthenium-catalyzed carbonylative C-H cyclization.[6] - o-Phenylenes, a class of conjugated oligomers via an iterative sequence of Suzuki-Miyaura coupling reactions.[7] - o,o,p-Oligophenylenes via palladium-catalyzed C-H arylation.[8] |
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