24018-00-6

Basic information

• Product Name: 2,2'-DIBENZOYLBIPHENYL
• Synonyms: 2,2'-DIBENZOYLBIPHENYL;TIMTEC-BB SBB008454;2,2''-DIBENZOYLBIPHENYL ---WHITE CRYSTALLINE---
• CAS NO: 24018-00-6
• Molecular Formula: C₂₆H₁₈O₂
• Molecular Weight: 362.42
• Mol File: 24018-00-6.mol
• Article Data: 7

Chemical Properties

• Melting Point: 172-173 °C
• Boiling Point: 578.1±43.0 °C(Predicted)
• Appearance: /
• Density: 1.165±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2,2'-DIBENZOYLBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-DIBENZOYLBIPHENYL(24018-00-6)
• EPA Substance Registry System: 2,2'-DIBENZOYLBIPHENYL(24018-00-6)

Safety Data

• Hazardous Substances Data: 24018-00-6(Hazardous Substances Data)

Usage

Chemical class

Aromatic ketones
Biphenyl derivative

Common uses

Fluorescent whitening agent in plastics, fibers, and coatings

Potential applications

Organic electronic devices and liquid crystal displays

Notable properties

High thermal stability and UV resistance

Industrial applications

Valuable and versatile compound

Upstream product

• 13047-06-8 o-bromobenzophenone 
• 602-15-3 9,10-diphenylphenanthrene 
• 102948-95-8 9,10-diphenyl-9,10-dihydrophenanthrene-9,10-diol 
• 58308-07-9 cis-9,10-diphenyldihydrophenanthrene-9,10-diol 
• 106568-93-8 α,α'-diphenyl<1,1'-biphenyl>-2,2'-dimethanol 
• 25187-00-2 2-iodobenzophenone 
• 100-52-7 benzaldehyde 
• 583-53-9 2,3-dibromobenzene 
• 100-58-3 phenylmagnesium bromide 
• 1210-05-5 Biphenyl-2,2'-dicarbaldehyde 
• 16002-63-4 phenylmagnesium iodide 
• 84-11-7 9,10-phenanthrenequinone 
• 60-29-7 diethyl ether 
• 5162-03-8 (2-chlorophenyl)(phenyl)methanone 

Downstream Products

• 18076-62-5 2,2'-bis(hydroxyldiphenylmethyl)biphenyl 
• 102948-95-8 9,10-diphenyl-9,10-dihydrophenanthrene-9,10-diol 
• 855195-97-0 2-[2-(α-hydroxy-benzhydryl)-phenyl]-benzophenone 
• 602-15-3 9,10-diphenylphenanthrene 
• 14718-07-1 10,10-diphenyl-10H-phenanthren-9-one 
• 106568-93-8 α,α'-diphenyl<1,1'-biphenyl>-2,2'-dimethanol 
• 122217-85-0 5,8-diphenyl-dibenzo[d,f][1,2]diazocine 
• 58308-07-9 cis-9,10-diphenyldihydrophenanthrene-9,10-diol 
• 58131-87-6 trans-9,10-dihydro-9,10-diphenyl-9,10-phenanthrenediol 
• 55006-98-9 2,2'-Bis(1-phenylvinyl)biphenyl 
• 18655-88-4 1,2-dithia-4,5-dimethyl-4-cyclohexene 
• 105930-72-1 Phenyl-(2'-thiobenzoyl-biphenyl-2-yl)-methanone 
• 106569-09-9 <1,1'-biphenyl>-2,2'-diylbis(phenylmethanone) dioxime 
• 106568-98-3 cis-<2'-(2-phenyl-1,3-dioxolan-2-yl)<1,1'-biphenyl>-2-yl>phenylmethanone oxime 

Relevant articles and documents

Sodium Hypochlorite Pentahydrate as a Reagent for the Cleavage of trans-Cyclic Glycols

Sodium hypochlorite pentahydrate (NaOCl·5H2O) can be used toward the efficient glycol cleavage of trans-cyclic glycols, which are generally resistant to this transformation. Interestingly, the reaction of cis-cyclic glycols with NaOCl·5H2O is slower than that observed for the corresponding trans-isomer. This trans selectivity is in sharp contrast to traditional oxidants used for glycol cleavage. Acyclic glycols can also react efficiently with NaOCl·5H2O to form their corresponding carbonyl compounds in high yield.

Nickel phosphate catalysts

Methods for coupling aryl halides or aryl sulfonates to produce biaryls or polyaryls using novel nickel phosphite catalysts are provided.

Syntheses and Chemistry of Some Dibenzazepines

5-Methyl-, 5,7-dimethyl-, and 5,7-diphenyl-substituted and unsubstituted 5H-dibenzazepines were prepared by two general routes from -2,2'-dicarboxaldehyde.The unsubstituted dibenzazepine was converted into 1a,9b-dihydrophenanthro9,10-