Methyl phenols

Die Bamberger-Umlagerung zu Amino-phenolen ist oft Ziel der elektrochemischen Reduktion, so z. B. bei der kathodischen Reduktion von 6-Chlor-2-nitro-toluol zu 2-Chlor-4-amino-3-methyl-phenol (an Pt bis 78% d.Th.)2 und von 2-Chlor-l-nitro-benzol zu 3-Chlor-4-amino-phenol (bis 63% d.Th.)3 (die leicht zu 1,4-Benzochinonen oxidiert werden konnen). 

Tri-tert-Butyl Phenol 4,41-Thio-bi s(6-tert-Butyl-3-methyl Phenol) 2,2 -Methylene-bi s(4-methyl -6-tert-Butyl Phenol) 2,2 -Methylene-bi s(4-ethyl -6-tert-Butyl Phenol) 330 150 131 133... 

Synonyms AI3-00075 Aptal Baktol Baktolan BRN 1237629 Candaseptic Caswell No. 185A CCRIS 1938 p-Chlor-/ 3-cresol Chlorocresol 4-Chlorocresol p-Chlorocresol 4-Chloro-/ 3-cresol 6-Chloro-/ 3-cresol 4-Chloro-l-hydroxy-3-methylbenzene 2-Chlorohydroxytoluene 2-Chloro-5-hydroxytoluene 4-Chloro-3-hydroxytoluene 6-Chloro-3-hydroxytoluene 4-Chloro-3-methyl-phenol /5-Chloro-3-methylphenol CMK EINECS 200-431-6 EPA pesticide chemical code 064206 3-Methyl-4-chlorophenol NSC 4146 Ottafact Parmetol Parol PCMC Peritonan Preventol CMK Raschit Raschit K Rasenanicon RCRA waste number U039 UN 2669. 

Synonyms 2-Methyl phenol 4-Methyl phenol 3-Methyl phenol Methyl phenol SANSS 1989 ... 

Dimethylamine chlordimefoim, chloromethiuron, chloroxuron, chlorotoluron, crimidine, dichlofluanid, dicrotophos, difenoxuron, dimefuron, dimethirimol, diphenamid, diuron, fenothiocarb, fenuron, ferbam, fluometuron, hexazinone, isoproturon, karbutilate, metoxuron, metribuzin, monuron, nicosulfuron, oxamyl, pirimicarb, pyrithiobac, thiram, tolyfluanid, triazamate, ziram 4 Dimethyl amino aniline fenaminosulf 2 Dimethyl amino 1,3 dichloro propane bensultap, thiocyclam N-N -Dimethylamino dimethyl aluminum nicosulfuron 2 Dimethyl amino 1,3 Dithiobenzyl propane thiocyclam 4 Dimethyl amino 3 methyl phenol aminocarb... 

C7H5N304S 4-carboxybenzenesulfonyl azide 17202-49-2 25.00 1.6056 2 10266 C7H6CI20 2,4-dichloro-3-methyl phenol 17788-00-0 25.00 1.3105 2... 

C7H603 benzenecarboperoxoic acid 93-59-4 23.33 1.4627 2 10566 C7H7FO 4-fluoro-3-methyl phenol 452-70-0 25.00 1.1340 1... 

C7H802 1,2-dihydroxy-4-methylbenzene 452-86-8 531.15 52.387 1,2 10972 C7H9NO 2-amino-3-methyl phenol 2835-97-4 480.51 42.014 2... 

For monochlorophenols, the parasubstituted isomer (4-chlorophenol) presents an absorption maximum at a wavelength higher than those of the other isomers (Fig. 61). Moreover, contrary to alkylphenols, the number of substituents has an influence on the position of the bands, increasing the shift with phenol (Table 5). Thus, pentachlorophenol leads to the greater shift value, whatever its form (undissociated or dissociated). For 4-chloro 3-methyl-phenol, the substituted methyl group seems to have no influence on the position of the band compared to the one of 4-chlorophenol. 

METHYL PHENOL or 4-METHYL PHENOL (1319-77-3) C,H,0 Combustible solid or liquid. Forms explosive mixture with air (flash point >178°F/>81°C autoignition temp 1038 to 1110°F/559 to 599 °C Fire Rating 2). Incompatible with strong acids, oxidizers, acetaldehyde, alkalis, aliphatic amines, amides, chlorosulfonic acid, nitric acid fuming sulfuric acid (oleum). Liquid attacks most plastics and rubber, although butyl rubber and Teflon have high resistance to permeation. Attacks many metals. 

METHYL PHENOL (1319-77-3) Combustible solid or liquid (flash point... 

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