Phenol 2,4,6-tris methyl

The aryl group substitution patterns found in lignans are delineated in Scheme 2. The rings may be mono-, di-, tri-, or tetrasubstituted by the common phenolic hydroxyl, methyl ether and methylenedioxy groups. With a few exceptions (isolated notably from mammalian sources), all lignans have an oxygenated substituent para... 

Solubility of Mixtures op a Tri Brom Phenol and s Tri Chlor Phenol in Methyl Alcohol at 25°. 

Stereospecific phenol coupling. Oxidation of (S)-(+)-7-hydroxy-l,5,6-tri-methyl-l,2,3,4-tetrahydronaphthalenc (1) in ether with K3Fe(CN)e in 0.2 N NaOH at 20 yields the optically active dimer shown to be the (SSytrans-enantiomer (2). The dl-(orm of the biaryl is also the major product of oxidation of (RS)-(l) together with smaller amounts of two diastereomeric forms. It... 

MES. See Methyl ethyl sulfide Mesitol, a,a, a"-trls (dimethylamino)-. See 2,4,6-Tris (dimethylaminomethyl) phenol Mesitylene. See 1,3,5-Tri methyl benzene Mesitylene, 2-benzoyl-. See 2,4,6-Trimethylbenzophenone 2-Mesitylenesulfonic acid, 4,4 -(1,4-anthraquinonylenediimino) di-, disodium salt. See Acid blue 80 Mesityl oxide... 

Benzyl trimethyl ammonium hydroxide Cetrimonium bromide Dimethyl diallyl ammonium chloride Laurtrimonium bromide Laurtrimonium chloride Methyl tributyl ammonium chloride Tetrabutyl ammonium bromide Tetrabutyl ammonium chloride Tetrabutyl ammonium fluoride Tetra-n-butyl ammonium hydrogen sulfate Tetra-n-butyl ammonium hydroxide Tetrabutyl ammonium iodide Tetrabutylphosphonium acetate, monoacetic acid Tetrabutylphosphonium bromide Tetrabutylphosphonium chloride Tetraethylammonium bromide Tetraethylammonium hydroxide Tetrakis (hydroxymethyl) phosphonium chloride Tetramethylammonium bromide Tetramethylammonium chloride Tetramethylammonium hydroxide Tetramethyl ammonium iodide Tetraphenyl phosphonium bromide Tetrapropyl ammonium bromide Tetrapropyl ammonium iodide Tributylamine Tributyl phosphine Tributyl (tetradecyl) phosphonium chloride Trioctyl (octadecyl) phosphonium iodide catalyst, phase-transfer Tetraethylammonium chloride Tetraoctylphosphonium bromide Tri-n-butyl methyl ammonium chloride Tri methyl phenyl ammonium hydroxide catalyst, phenolics Triethylamine... 

Methyl alcohol formaldehyde scavenger Aminoethyl propanediol formaldehyde scavenger, curing phenolics Tris (hydroxymethyl) aminomethane formaldehyde source... 

UVA 2-hydroxy-4-octyloxybenzophenone 2-hydroxy-4-methoxybenzophenone 2-(2H-benzotriazol-2-yl)-p-cresol 2-(2H-benzotriazole-2-yl)-4,6-di-tert-pentylphenol 2-(2H-benzotriazole-2-yl)-4-(1,1,3,3-tetraethylbutyl)phenol 2,4-di-tert-butyl-6-(5-chloro-2H-benzotriazole-2-yl)-phenol 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy) phenol ethyl-2-cyano-3,3-diphenylacrylate HAS 1,3,5-tri-azine-2,4,6-triamine, N,N [1,2-ethane-diyl-bis[[[4,6-bis[butyl-(1,2,6,6-pentamethyl-4-piperidinyl)amino]-1,3,5-triazine-2-yl] imino]-3,1 -propanediyi] bis[N ,N -dibutyl-N ,N -bis(1,2,2,6,6-pentamethyl-4-piperidinyl)- bis(2,2,6,6-tetramethyl-4-piper-idyl) sebacate 2,2,6,6-tetramethyl-4-piperidinyl stearate N,N -bisformyl-N,N -bis-(2,2,6,6-tetramethyl-4-piperidinyl)-hexamethylendiamine alkenes, C20-24-.alpha.-, polymers with maleic anhydride, reaction products with 2,2,6,6-tet-ramethyl-4-piperidinamine 1,6-hexanediamine, N, N -bis(2,2,6,6-tetramethyl-4-piperidinyl)-, polymers with 2,4-di-ohloro-6-(4-morpholinyl)-1,3,5-triazine 1,6-hexanediamine, N,N -bis(2,2,6,6-tetramethyl-4-piperidinyl)-, polymers with morpholine-2,4,6-trichloro-1,3,5-triazine reaction products, methylated Phenolic antioxidants ethylene-bis(oxyethylene)-bis(3-(5-tert-butyl-4-hydroxy-m-tolyl)-propionate) 2,6,-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5,-triazine-2-ylamino) phenol pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate) 2-(1,1 -dimethylethyl)-6-[[3-(1,1 -dimethylethyl)-2-hydroxy-5-methylphenyl] methyl-4-methylphenyl acrylate isotridecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate 2,2 -ethylidenebis (4,6-di-tert-butylphenol) 2,2 -methylenebis(4-ethyl-6-tertbutylphenol) 3,5-bis(1,1-dimethyethyl)-4-hydroxy-benzenepropanoic acid, C13-15 alkyl esters phenol, 4-methyl-, reaction products with dicyclopen-tadiene and isobutene Phosphite trinonylphenol phosphite isodecyl diphenyl phosphite... 

Additives used in final products Fillers calcium carbonate, calcium hydroxide, calcium oxide, carbon black, polymeric beads, polystyrene particles, zinc oxide Plasticizers 1-isobutyrate benzyl phthalate, 2,2,4-tri-methyl-1,3-pentanediol, alkyl sulfonic acid esters of phenol and/or cresol, benzyl butyl phthalate, chlorinated paraffins, hydrogenated perphenyl, isooctyl benzyl phthalate Curatives metal peroxides, oxy salts (e.g., dioxides of lead, manganese, calcium, etc.) ... 

The reaction between liquid polysulfide polymers and epoxies is catalyzed by organic amines, for example, dimethylamine methyl phenol, tri-dimethylami-nomethyl phenol, diethylenetriamine, and benzyldimethylamine. The reaction of liquid polysulfide polymer with an epoxy resin and a primary amine is... 

The method was applied to a polymer suspected to contain one or more of the following additives (1) Topanol CA (4,4, 4" - butylene -1,1 3 tris (trimethyl-6-ferr butyl phenol). (2) DLTDP (dilauryl thiodipropionate) and (3) lonox 330 (1,3,5 tri methyl -2,4,6-tri (3,5-di-/cr/-butyl)-4-hydroxy benzyl) benzene. 

The above is a general procedure for preparing trialkyl orthophosphates. Similar yields are obtained for trimethyl phosphate, b.p. 62°/5 mm. triethyl phosphate, b.p. 75-5°/5 mm. tri-n-propyl phosphate, b.p. 107-5°/5 mm. tri-Mo-propyl phosphate, b.p. 83-5°/5 mm. tri-wo-butyl phosphate, b.p. 117°/5-5 mm. and tri- -amyl phosphate, b.p. 167-5°/5 mm. The alkyl phosphates are excellent alkylating agents for primary aromatic amines (see Section IV,41) they can also be ua for alkylating phenols (compare Sections IV,104-105). Trimethyl phosphate also finds application as a methylating agent for aliphatie alcohols (compare Section 111,58). 

CF3COOH, 2.5% phenol, 30°, 2 h, 65% yield. Zervas and co-workers tried many conditions for the acid-catalyzed formation and removal of the 5-diphenyl methyl, 5-4,4 -dimethoxydiphenylmethyl, and 5-tripheny I methyl thioethers. The best conditions for the 5-diphenylmethyl thioether are shown above. Phenol or anisole act as cation scavengers. 

Treatment of commercially available and symmetrical 3,4,5-tri-methoxytoluene (37) with iodine, periodic acid, and acetic acid under the conditions of Suzuki19 results in the formation of symmetrical diiodide 38 in 93 % yield. Although only one of these newly introduced iodine atoms is present in intermediate 13, both play an important role in this synthesis. Selective monodemethylation of 38 with boron trichloride furnishes phenol 39 in 53% yield together with 13 % of a regioisomer. Evidently, one of the Lewis-basic iodine substituents coordinates with the Lewis-acidic boron trichloride and directs the cleavage of the adjacent methyl ether... 

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