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1- Methyl-3- -urea sulfone

Mercaptoacetic Add 2-Mercaptobenzoic Acid Methane Methanol Methionine Methotrexate Methylene Blue A-Methyl Glycine 5-Methylindole Methyl Isocyanate Methylmalonic Add Methyl Methacrylate Methylmethane Sulfonate Methyl Thiocyanate A-Methyl Thiourea Methyl Urea Naphthalene Nicotinic Acid Ornithine Orotic Acid Oxalic Acid Oxindole Palmitic Acid Paraldehyde Pentobarbital Phenol... [Pg.329]

Sodium dodecylbenzenesulfonate Sodium lauryl sulfate ,Sodium methyl oleoyl sulfonate Sodium myristoyl sarcosinate Sodium a olefin sulfonate Sodium oleic sulfate Sodium oleic sulfonate Trideceth-3 Trideceth-6 Trideceth-9 Trideceth-12 Urea penetrant, adhesives... [Pg.5508]

M. Shi and Y.-L. Shi reported the synthesis and application of new bifunctional axially chiral (thio) urea-phosphine organocatalysts in the asymmetric aza-Morita-Baylis-Hillman (MBH) reaction [176, 177] of N-sulfonated imines with methyl vinyl ketone (MVK), phenyl vinyl ketone (PVK), ethyl vinyl ketone (EVK) or acrolein [316]. The design of the catalyst structure is based on axially chiral BINOL-derived phosphines [317, 318] that have already been successfully utilized as bifunctional catalysts in asymmetric aza-MBH reactions. The formal replacement of the hydrogen-bonding phenol group with a (thio)urea functionality led to catalysts 166-168 (Figure 6.51). [Pg.301]

Janus [11] has recently shown that urea can also be smoothly methylated with methyl toluene-p-sulfonate at 80°-90°C to give good yields of crystalline 2-methylpseudourea toluene-p-sulfonate. [Pg.341]

Another way of producing a low proton activity at the amalgam surface is to add a suitable polar, aprotic compound to the medium. Suitable compounds include urea and its derivatives, amides, lactams, sulfoxides, and sulfones, such as 1,3-dimethylurea, ethyle-neurea, biuret, formamide, A-methyl formamide, acetamide, 5-butyrolactam, dimethyl sulfoxide, di- -butyl sulfoxide, and dimethyl sulfone [41,42]. Dimethylformamide (DMF) or acetonitrile, besides some of the compounds just mentioned, may be used as solvents [43,44]. One function of the added compound is to establish an aprotic reaction layer at the amalgam surface by selective adsorption of the compound on the amalgam another is to solvate the ion pair (consisting of the radical ion and the cation) in a suitable way. [Pg.1150]

Addition of sulfides and sulfones to acid derivatives has been investigated by Agawa. Phenyl and methyl (trimethylsilyl)methyl sulfides and sulfones added to amides (323) to produce the aminovinyl sulfides (324 equation 74) and sulfone (326 equation 7S). The reactions proceeded in good yield with some examples of stereocontrolled synthesis of the ( )-isomer. Other acid derivatives such as esters, carbonates and ureas were investigated, but gave inconsistent results. [Pg.787]

The best known and most widely used diazoalkane is diazomethane (95 equation 39). Preparative methods for diazomethane involve, in general, the nitrosation of a methylamine derivative (93), followed by cleavage under alkaline conditions. Methylamine derivatives used have included the urethanes, ureas,carboxamides, sulfonamides, guanidines and even the methylamine adducts of unsaturated ketones and sulfones. N-nitroso-N-methyl p-toluenesulfonamide (Diazald, Aldrich) is currently the most commonly used diazomethane precursor. Diazomethane is both toxic and explosive. Although in the past it has been purified by codistillation with ether, it is now usually generated, stored and used as an ether solution without distillation. [Pg.120]

Heterocycles Acetylacetone. N-Aminophthalimide. Boron trichloride. Dichloro-formoxime. Oicyanodiamide. Dicyclohexylcarbodiimide. Dietboxymethyl acetate. Diethyl oxalate. Diketene. Dimethylformaniide diethylacetal. Diphenyldiazomethene. Ethyl ethoxy-methylenecyanoacetate. Formaldehyde. Formamide. Formamidine acetate. Formic acid. Glyoxal. Hydrazine. Hydrazoic acid. Hydroxylamine. Hydroxylamine-O-sulfonic acid. Methyl vinyl ketone. o-Phenylenediamine. Phenylhydrazine. Phosphorus pentasullide. Piperidine. Folyphosphoric acid. Potassium diazomethanedisulfonate. Sodium ethoxide. Sodium nitrite. Sodium thiocyanate. Tetracyanoethylene. Thiosemicarbozide. Thiourea. Triethyl orthoformate. Tris-formaminomethane. Trityl perchlorate. Urea. Vinyl triphenyl-phosphonium bromide. [Pg.662]

Omicure 24. See Toluene bis (dimethyl urea) Omicure 24EMI. See 2-Ethyl-4-methyl imidazole Omicure 33DDS. See 3,3 -Diaminodiphenyl sulfone... [Pg.2996]

Poly (melamine-co-formaldehyde), methylated. See Melamine-formaldehyde resin, methylated Poly (melamine-co-formaldehyde), methylated/butylated. See Melamine-formaldehyde resin, methylated-butylated Polymene AZ. See PEG castor oil Polymer C . See Polypropylene Polymer SBOCP. See Cocamidopropyl dimethylammonium C8-16 isoalkylsuccinyl lactoglobulin sulfonate Polymer Additive GH. See Polyoxyisobutylene/methylene urea copolymer Polymeric biuret of HDI Polymeric HDI Polymeric HMDI. See Hexamethylene diisocyanate biuret Polymeric MDI... [Pg.3529]

Stannous octoate Stearamide MEA Stearyl methacrylate 3-(N-Styrylmethyl-2-aminoethylamino) propyltrimethoxysilane hydrochloride Sucrose distearate Sulfated neatsfoot oil Sulfated olive oil Synthetic wax Talc Tall oil Tallowamide DEA Tallowamine acetate Tetra-n-butoxysilane Tetrakis (2-ethoxyethoxy) silane Tetrakis (2-methoxyethoxy) silane Tetramethoxysilane 2,2,4,4-TetramethyM, 3-cyclobutanediol 1,1,4,4-Tetramethyldichlorodisilethylene 1,1,3,3-Tetramethyldisiloxane Tetramethylsilane Tetramethylthiuram disulfide Tetra-n-propoxysilane Tributoxyethyl phosphate Tributyl phosphate Trichlorosilane Triethoxysilane N-[3-(Triethoxysilyl)-propyll 4,5-dihydroimidazole N-(Triethoxysilylpropyl) urea Triethylchlorosilane Triethyl phosphate Triethylsilane Trilauryl trithiophosphite Trilinoleic acid 1-Trimethoxysilyl-2-(chloromethyl) phenylethane Trimethoxysilylpropyidiethylene triamine N-Trimethoxysilylpropyl-N,N,N-trimethyl ammonium chloride Trimethylethoxysilane 2,6,8-Trimethylnonyl-4-alcohol Trimethylolpropane tricocoate 2,2,4-Tri methyl-1,3-pentanediol Trimethylsilyl acetamide o-Trimethylsilyl acetate Trimethylsilyl imidazole Trimethylsilyl iodide Trimethylsilyinitrile Trimethylsilyl trifluoromethane sulfonate Vermiculite Vinyidimethylchlorosilane ... [Pg.5431]

Figure 1 Polymer interpretation chart. PAI, polyamideimide PC, polycarbonate UP, unsaturated polyester PDAP, diarylate phtalate resin VC-VAc, vinyl chloride-vinyl acetate copolymer PVAc, polyvinyl acetate PVFM, polyvinyl formal PUR, polyurethane PA, polyamide PMA, methacrylate ester polymer EVA, ethylene-vinyl acetate copolymer PF, phenol resin EP, epoxide resin PS, polystyrene ABS, acrylonitrile-butadiene-styrene copolymer PPO, polyphenylene oxide P-SULFONE, poly-sulfone PA, polyamide UF, urea resin CN, nitrocellulose PVA, polyvinyl acetate MC, methyl cellulose MF, melamine resin PAN, polyacrylonitrile PVC, polyvinyl chloride PVF, polyvinyl fluoride CR, polychloroprene CHR, polyepichlorohydrin SI, polymethylsiloxane POM, polyoxy-methylene PTFE, polytetrafluoroethylene MOD-PP, modified PP EPT, ethylene-propylene terpolymer EPR, ethylene-propylene rubber PI, polyisoprene BR, butyl rubber PMP, poly(4-methyl pentene-1) PE, poly(ethylene) PB, poly(butene-l). (Adapted from Ref. 22, p. 50.)... Figure 1 Polymer interpretation chart. PAI, polyamideimide PC, polycarbonate UP, unsaturated polyester PDAP, diarylate phtalate resin VC-VAc, vinyl chloride-vinyl acetate copolymer PVAc, polyvinyl acetate PVFM, polyvinyl formal PUR, polyurethane PA, polyamide PMA, methacrylate ester polymer EVA, ethylene-vinyl acetate copolymer PF, phenol resin EP, epoxide resin PS, polystyrene ABS, acrylonitrile-butadiene-styrene copolymer PPO, polyphenylene oxide P-SULFONE, poly-sulfone PA, polyamide UF, urea resin CN, nitrocellulose PVA, polyvinyl acetate MC, methyl cellulose MF, melamine resin PAN, polyacrylonitrile PVC, polyvinyl chloride PVF, polyvinyl fluoride CR, polychloroprene CHR, polyepichlorohydrin SI, polymethylsiloxane POM, polyoxy-methylene PTFE, polytetrafluoroethylene MOD-PP, modified PP EPT, ethylene-propylene terpolymer EPR, ethylene-propylene rubber PI, polyisoprene BR, butyl rubber PMP, poly(4-methyl pentene-1) PE, poly(ethylene) PB, poly(butene-l). (Adapted from Ref. 22, p. 50.)...
Tg measurements have been performed on many other polymers and copolymers including phenol bark resins [71], PS [72-74], p-nitrobenzene substituted polymethacrylates [75], PC [76], polyimines [77], polyurethanes (PU) [78], Novolac resins [71], polyisoprene, polybutadiene, polychloroprene, nitrile rubber, ethylene-propylene-diene terpolymer and butyl rubber [79], bisphenol-A epoxy diacrylate-trimethylolpropane triacrylate [80], mono and dipolyphosphazenes [81], polyethylene glycol-polylactic acid entrapment polymers [82], polyether nitrile copolymers [83], polyacrylate-polyoxyethylene grafts [84], Novolak type thermosets [71], polyester carbonates [85], polyethylene naphthalene, 2,6, dicarboxylate [86], PET-polyethylene 2,6-naphthalone carboxylate blends [87], a-phenyl substituted aromatic-aliphatic polyamides [88], sodium acrylate-methyl methacrylate multiblock copolymers [89], telechelic sulfonate polyester ionomers [90], aromatic polyamides [91], polyimides [91], 4,4"-bis(4-oxyphenoxy)benzophenone diglycidyl ether - 3,4 epoxycyclohexyl methyl 3,4 epoxy cyclohexane carboxylate blends [92], PET [93], polyhydroxybutyrate [94], polyetherimides [95], macrocyclic aromatic disulfide oligomers [96], acrylics [97], PU urea elastomers [97], glass reinforced epoxy resin composites [98], PVOH [99], polymethyl methacrylate-N-phenyl maleimide, styrene copolymers [100], chiral... [Pg.97]


See other pages where 1- Methyl-3- -urea sulfone is mentioned: [Pg.444]    [Pg.197]    [Pg.155]    [Pg.172]    [Pg.955]    [Pg.796]    [Pg.342]    [Pg.249]    [Pg.325]    [Pg.487]    [Pg.1009]    [Pg.796]    [Pg.445]    [Pg.445]    [Pg.796]    [Pg.496]    [Pg.487]    [Pg.47]    [Pg.223]    [Pg.899]    [Pg.28]    [Pg.121]    [Pg.1526]    [Pg.2160]    [Pg.4794]    [Pg.5646]    [Pg.2672]    [Pg.316]    [Pg.316]    [Pg.200]   


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1- Methyl-3- -urea

Methyl sulfone

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