61608-94-4

Basic information

• Product Name: Ethanone, 1-[2-(phenylmethyl)phenyl]-
• CAS NO: 61608-94-4
• Molecular Formula: C15H14O
• Molecular Weight: 210.276
• Mol File: 61608-94-4.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-(phenylmethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-(phenylmethyl)phenyl]-(61608-94-4)
• EPA Substance Registry System: Ethanone, 1-[2-(phenylmethyl)phenyl]-(61608-94-4)

Safety Data

• Hazardous Substances Data: 61608-94-4(Hazardous Substances Data)

Upstream product

• 64-19-7 acetic acid 
• 94-41-7 benzalacetophenone 
• 23450-18-2 2-benzyl-1-bromobenzene 
• 18982-54-2 o-bromobenzyl alcohol 
• 6630-33-7 ortho-bromobenzaldehyde 
• 937792-44-4 1-benzyl-2-ethynylbenzene 
• 937792-81-9 ((2-benzylphenyl)ethynyl)trimethylsilane 
• 2142-69-0 2-bromophenyl methyl ketone 
• 100-44-7 benzyl chloride 
• 98-86-2 acetophenone 
• 100-51-6 benzyl alcohol 
• 79-37-8 oxalyl dichloride 
• 612-35-1 2-Benzylbenzoic acid 
• 89-98-5 2-chloro-benzaldehyde 

Downstream Products

• 154708-65-3 4,4,4-trifloro-1-<2-(phenylmethyl)benzoyl>-1,3-butanedione 
• 51012-66-9 2-benzyl-2-bromoacetophenone 
• 5371-55-1 1-hydroxyimino-1,3-diphenylpropane 
• 779-02-2 9-methylanthracene 
• 1253196-53-0 (E)-1-(2-benzylphenyl)-3-(dimethylamino)prop-2-en-1-one 
• 1021429-84-4 1-(2-benzylphenyl)-3-phenyl-1,3-butanedione 
• 135426-60-7 (S)-4-[[[4-(4-Fluorophenyl)-2-(1-methylethyl)-6-[2-(phenylmethyl)phenyl]-3-pyridinyl]ethynyl]hydroxyphosphinyl]-3-hydroxybutanoic acid, disodium salt 
• 135426-36-7 6-(2-Benzyl-phenyl)-3-(2,2-dibromo-vinyl)-4-(4-fluoro-phenyl)-2-isopropyl-pyridine 
• 135426-15-2 4-(4-Fluorophenyl)-2-(1-methylethyl)-6-[2-(phenylmethyl)phenyl]-3-pyridinemethanol 
• 120934-79-4 methyl 2-methyl-4-(2-(phenylmethyl)-benzoyl)-1H-pyrrole-3-carboxylate 
• 120935-82-2 methyl 1-(((1,1-Dimethylethoxy)carbonyl)amino)-3-(methoxycarbonyl)-5-methyl-4-(2-(phenylmethyl)benzoyl)-1H-pyrrole-2-acetate 
• 154708-58-4 4-(2-Benzyl-benzoyl)-1-tert-butoxycarbonylamino-5-hydroxy-2-methyl-5-trifluoromethyl-4,5-dihydro-1H-pyrrole-3-carboxylic acid methyl ester 
• 154708-57-3 methyl 1-tert-butoxycarbonylamino-2,5-dimethyl-4-<2-(phenylmethyl)benzoyl>-1H-pyrrole-3-carboxylate 

Relevant articles and documents

Cobalt-Catalyzed Reductive Cross-Coupling Between Benzyl Chlorides and Aryl Halides

A new protocol for the direct reductive cobalt-catalyzed arylation of benzyl chlorides has been developed in order to form functionalized diarylmethanes. A variety of reactive groups either on the aryl or the benzyl halide was employed. This represents the first cobalt-catalyzed reductive cross-coupling which does not require any ligand and pyridine. A reaction pathway is proposed involving a radical benzyl species. (Figure presented.).

PREPARATION METHOD OF ANTHRACENE DERIVATIVES CATALYZED BY BISMUTH SALTS

The present invention relates to a method for preparing an anthracene derivative by using a bismuth catalyst. The invention relates to a method for preparing an anthracene derivative simply and efficiently by using a bismuth catalyst and an acid additive. The preparation method allows obtaining a target material in a short time at a high yield by using a bismuth catalyst and an acid additive. Then, the prepared anthracene derivative may be used in a synthesis of intermediate in fine chemicals including pharmaceuticals and agricultural chemicals, and a synthesis of a variety of polymer materials having optical properties.COPYRIGHT KIPO 2015

Direct method for carbon-carbon bond formation: The functional group tolerant cobalt-catalyzed alkylation of aryl halides

(Figure Presented). A new protocol for the direct cobaltcatalyzed alkylation of aryl halides has been developed that proceeds smoothly in the presence of phosphanes or bipyridines as ligands with a variety of alkyl halides, including challenging alkyl electrophiles bearing β hydrogen atoms (see scheme). Sensitive functional groups are tolerated on both coupling partners, thus, significantly extending the general scope of transition-metal-catalyzed alkylation of aryl halides.