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一般說明
4-Phenylphenol (4-hydroxybiphenyl, 4-HBP), a biaryl compound, is a weakly acidic[1] 4-arylphenol. A study on its crystalline structure has been reported.[2] Its rapid, green synthesis via a Pd(0)-catalyzed Suzuki cross-coupling reaction in water has been reported.[3] The standard molar enthalpy of formation of 4-phenylphenol has been evaluated using combustion calorimetry.[4] The solid-matrix luminescence properties for 4-phenylphenol adsorbed on filter paper has been investigated.[5] A study conducted using the yeast two-hybrid assay suggests that it shows estrogenic activity.[6]
應用
4-Phenylphenol may be used in the following studies:
- As a reactant in the synthesis of new azobenzene sulfonic acid dopants by diazotized coupling reaction with sulphanilic acid diazonium salt.[7]
- As a starting material in the synthesis of 2,6-poly(4-phenylphenol).[8]
- As a ligand in the synthesis of aluminum (III) bis(2-methyl-8-quninolinato)-4-phenylphenolate (BAlq).[9]
訊號詞
Warning
危險聲明
危險分類
Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1B
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 2
閃點(°F)
320.0 °F - closed cup
閃點(°C)
160 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
客戶也查看了
Thermochemistry of phenols: experimental standard molar enthalpies of formation of 2-phenylphenol, 4-phenylphenol, 2, 6-diphenylphenol, and 2, 2'-and 4, 4'-dihydroxybiphenyl.
Verevkin SP.
The Journal of Chemical Thermodynamics, 30(3), 389-396 (1998)
" Greening Up" the Suzuki Reaction.
Aktoudianakis E, et al.
Journal of Chemical Education, 85(4), 555-555 (2008)
Characterization of electronic structure of aluminum (III) bis (2-methyl-8-quninolinato)-4-phenylphenolate (BAlq) for phosphorescent organic light emitting devices.
Chu TY, et al.
Chemical Physics Letters, 404(1), 121-125 (2005)
The polymerization of 4-phenylphenol catalyzed by laccase.
Zhou P and Fu S.
Acta Polymerica Sinica / Gao Fen Zi Xue Bao, 4, 614-616 (2004)
Preparation of some aryl α-L-arabinofuranosides as substrates for arabino-furanosidase.
Kelly MA, et al.
Carbohydrate Research, 181, 261-266 (1988)
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