140627-35-6

Basic information

• Product Name: 2-phenylbenzene-1,4-diol
• Synonyms: 2-phenylbenzene-1,4-diol
• CAS NO: 140627-35-6
• Molecular Formula: C12H10O2
• Molecular Weight: 0
• Mol File: 140627-35-6.mol
• Article Data: 21

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-phenylbenzene-1,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenylbenzene-1,4-diol(140627-35-6)
• EPA Substance Registry System: 2-phenylbenzene-1,4-diol(140627-35-6)

Safety Data

• Hazardous Substances Data: 140627-35-6(Hazardous Substances Data)

Upstream product

• 107449-13-8 O-(2-biphenylyl)hydroxylamine 
• 67-56-1 methanol 
• 42860-77-5 4-hydroxy-4-phenyl-cyclohexa-2,5-dienone 
• 4197-75-5 cyclohexyl-1,4-benzenediol 
• 92-52-4 biphenyl 
• 90-43-7 2-Phenylphenol 
• 831-82-3 4-Phenoxyphenol 
• 363-03-1 2-phenyl-1,4-benzoquinone 
• 36590-52-0 N-phenyl-p-chlorobenzohydrazonoyl chloride 
• 25939-01-9 p-toluoyl chloride phenylhydrazone 
• 917-54-4 methyllithium 
• 15424-14-3 N-phenylbenzohydrazonoyl chloride 
• 64-17-5 ethanol 
• 127-09-3 sodium acetate 

Downstream Products

• 1267658-48-9 C₁₈⁽¹¹⁾CH₂₁NO₃ 
• 1267658-49-0 [carbonyl-11C]-N-cyclohexyl-5-hydroxy[1,1'-biphenyl]-3-ylcarbamic acid ester 
• 1416734-93-4 C₁₇⁽¹¹⁾CH₁₉NO₃ 
• 1416734-94-5 C₁₆⁽¹¹⁾CH₁₇NO₃ 
• 1057679-58-9 4-([1,1'-biphenyl]-3-yl)morpholine 

Relevant articles and documents

Metal-free reduction of unsaturated carbonyls, quinones, and pyridinium salts with tetrahydroxydiboron/water

A series of unsaturated carbonyls, quinones, and pyridinium salts have been effectively reduced to the corresponding saturated carbonyls, dihydroxybenzenes, and hydropyridines in moderate to high yields with tetrahydroxydiboron/water as a mild, convenient, and metal-free reduction system. Deuterium-labeling experiments have revealed this protocol to be an exclusive transfer hydrogenation process from water. This journal is

Oxidative coupling and hydroxylation of phenol over transition metal and acidic zeolites: Insights into catalyst function

Reaction of phenol with hydrogen peroxide over H-MFI, Fe-MFI, H-BEA, Fe-BEA and TS-1 zeolite catalysts was investigated. Over H-BEA, biphenyl product was observed. It is suggested, that the larger pore size of H-BEA facilitates coupling of two phenol molecules. Two distinct reaction mechanisms are proposed for acid and redox catalysts.

A direct approach to 5-hydroxybenzofurans via a platinum-catalyzed domino rearrangement/5-endo-dig cyclization reaction of quinols

(Chemical Equation Presented) A highly efficient and atom-economical construction of 2-substituted 5-hydroxybenzofurans was accomplished by employing a platinum-catalyzed domino dienone-phenol rearrangement/5-endo-dig cyclization reaction of quinols beari