4-methoxyphenyl 4-methylphenyl

Chemical Name (2-hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone Common Name 2-hydroxy-4-methoxy-4 -methylbenzophenone... 

Methoxyphenyl 4-Methylphenyl Tellurium Dichloride3 In a 100 ml flask fitted with a reflux condenser arc placed 8.5 g (25 mmol) of 4-methoxyphenyl tellurium trichloride, 11.7 g (71 mmol) of 4-methyl-phenyltrimethylsilane, and 6 ml of dioxanc. The mixture is heated under reflux for 4 h and the cooled mixture is then diluted with 40 ml of hexane. The brown precipitate is filtered off and recrystallized twice from benzene/hexane (1/2, v/v) yield 5.7 g (58%) m.p. 165°. 

CAS 1641-17-4 EINECS/ELINCS 216-688-2 Synonyms 2-Hydroxy-4-methoxy-4 -methylbenzophenone (2-Hydroxy-4-methoxyphenyl) (4-methylphenyl) methanone Methanone, (2-hydroxy-4-methoxyphenyl) (4-methylphenyl)- Mexenone Classification Benzophenone deriv. 

Synonyms 2-hydroxy-(4-methoxyphenyl)(4-methylphenyl)methanone 2-hydroxy-methoxymethylbenzophenone Benzophenone 10 Mexenone Uvistat... 

Hydroxy-2,5-dimethylphenyl)(4-hydroxyphenyl)methanone, 435 (4-Hydroxy-2,6-dimethylphenyl)(4-hydroxyphenyl)methanone, 435 (4-Hydroxy-3,5-dimethylphenyl)(2-hydroxyphenyl)methanone, 435 (4-Hydroxy-3,5-dimethylphenyl)(3-hydroxyphenyl)methanone, 435 (4-Hydroxy-3,5-dimethylphenyl)(4-hydroxyphenyl)methanone, 436 [4-Hydroxy-3-(hydroxymethyl)phenyl](3-methylphenyl)methanone, 282 (2-Hydroxy-3-methoxy-5-methylphenyl)phenylmethanone, 97 (2-Hydroxy-3-methoxy-6-methylphenyl)phenylmethanone, 97 (2-Hydroxy-4-methoxy-3-methylphenyl)pheny1methanone, 97 (2-Hydroxy-4-methoxy-5-methylphenyl)phenylmethanone, 98 (2-Hydroxy-4-methoxy-6-methylphenyl)phenylmethanone, 98 (2-Hydroxy-5-methoxy-4-methylphenyl)phenylmethanone, 98 (2-Hydroxy-6-methoxy-4-methylphenyl)phenylmethanone, 99 (4-Hydroxy-2-methoxy-6-methylphenyl)phenylmethanone, 99 (5-Hydroxy-4-methoxy-2-methylphenyl)phenylmethanone, 99 (2-Hydroxy-4-methoxyphenyl)(2-methylphenyl)methanone, 282 (2-Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone, 282 (4-Hydroxy-3-methoxyphenyl)(2-methylphenyl)methanone, 283 (4-Hydroxy-3-methoxyphenyl)(4-methylphenyl)methanone, 283 (2-Hydroxy-3-methylphenyl)(4-methoxyphenyl)methanone, 283 (2-Hydroxy-4-methylphenyl)(4-methoxyphenyl)methanone, 283 (2-Hydroxy-5-methylphenyl)(2-methoxyphenyl)methanone, 284 (2-Hydroxy-5-methylphenyl)(3-methoxyphenyl)methanone, 284 (2-Hydroxy-5-methylphenyl)(4-methoxyphenyl)methanone, 284 (4-Hydroxy-3-methylphenyl)(2-methoxyphenyl)methanone, 285 (4-Hydroxy-3-methylphenyl)(4-methoxyphenyl)methanone, 285 [3-(Hydroxymelhyl)phenyl](4-Hydroxy-3-methylphenyl)methanone, 285 (4-Hydroxyphenyl)(2-methoxy-5-methylphenyl)methanone, 177... 

Chloro-4-methoxyphenyl)(4-nitrophenyl)methanone, 605 (2-Chloro-4-methoxyphenyl)(4-methylphenyl)methanone, 649 (2-Chloro-4-methoxyphenyl)(4-chlorophenyl)methanone, 606 (2-Chloro-4-methoxyphenyl)(4-nitrophenyl)methanone, 645 (5-Chloro-2-methoxyphenyl)(4-methoxyphenyl)methanone, 633 (5-Chloro-2-methoxyphenyl)(4-chlorophenyl)methanone, 607 (5-Chloro-2-methoxyphenyl)(4-nitrophenyl)methanone, 605 (4-Chlorophenyl)(2-methoxyphenyl)methanone, 588 (4-Chloro-2-methoxyphenyl)phenyhnethanone, 578 (2,5-Dimethoxyphenyl)(4-methoxyphenyl)methanone, 571 (2-Chloro-4-hydroxyphenyl)phenyhnethanone, 577 (2-Hydroxy-4-methylphenyl)(4-methylphenyl)methanone, 616 (3-Methoxyphenyl)(4-methylphenyl)methanone, 595 (4-Hydroxyphenyl)[4-(methylthio)phenyl]methanone, 597 [2-Hydroxy-4-(pentyloxy)phenyl]phenylmethanone, 584 (5-Chloro-2-hydroxyphenyl)(4-nitrophenyl)methanone, 605 (4-Fluorophenyl)(2,3,4-trihydroxyphenyl)methanone, 639 Cyclohexyl(2,4,6-trihydroxyphenyl)methanone, 644 (3-Amino-2,4-dihydroxyphenyl)phenylmetlianone, 625 (3-Bromo-4-hydroxyphenyl)phenylmethanone, 577 [2,6-Dihydroxy-4-methoxy-3-(3-methyl-2-butenyl)-5-[5-methyl-2-(l-methylethenyl)-5-hexenyl]phenyl](3-hydroxyphenyl)methanone (-),641... 

Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone, 618 [212902-63-1] 4-(3,4-Dihydroxy-5-nitrobenzoyl)benzoic acid, 630 [215380-62-4] (5-Bromo-2-hydroxyphenyl)(4-methylphenyl)methanone, 608... 

Vpse couplings of about 730 Hz have been determined by Schaarsch-midt et for the parent 2-diphenylphosphoroselenoyl-(2-( )-phenyl-vinyl)ferrocene and its 4-chlorophenyl, 4-methoxyphenyl, 4-methylphenyl, 4-cyanophenyl and 4-acetylphenyl derivatives. The coupling values do not vary significantly within the series and are very close to that reported for Ph3P=Se. This led the authors to the conclusion that the electronic influence of substituents is limited to the ferrocene and hence no interaction with the phosphorous atom could be observed. This opens the possibility to modify the electronic characteristics of both donor functionalities (alkene and phosphine) independently from each other. 

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