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Amides sulfonated

Uses fungicide, cereals, ornamentals Trade names Plantvax (Uniroyal) Type oxathiin, amide, sulfone... [Pg.739]

Buthiobate heterocyclic nitrogen, pyridine Butocarboxim oxime amide, sulfone Butoxycarboxim oxime amide Butralin dinitroaniline Butylate thiocarbamate... [Pg.1005]

Oxine-copper heterocyclic nitrogen, quinoline Oxolinic acid heterocyclic nitrogen, quinoline Oxycarboxin oxathiin, amide, sulfone Oxydemeton-methyl phosphoro organic, phosphoro thioate... [Pg.1010]

Nonaqueous solvents — Nonaqueous solvents are liquids, relevant for the preparation of solutions other than water. They can be classified in several ways protic (e.g., alcohols, acids, amines, mercaptans, i.e., having labile protons) vs. aprotic polar vs. nonpolar (e.g., paraffins, olefins, aromatic derivatives, or benzene) organic (e.g. esters, ethers, alkylcarbonates, nitriles, amides, sulfones) vs. inorganic (chalcogenides such as SOCI2, SO2CI2). Nonaqueous solvents may be superior to water in the following aspects ... [Pg.454]

Figure 38 Synthesis of PAEKs incorporating various types of functional groups. Types of X groups incorporated imide, amide, sulfone, ester, azo, quinoxaline, aliphatic, fluoroaliphatic, fluoroaromatic. (From Ref. 164.)... Figure 38 Synthesis of PAEKs incorporating various types of functional groups. Types of X groups incorporated imide, amide, sulfone, ester, azo, quinoxaline, aliphatic, fluoroaliphatic, fluoroaromatic. (From Ref. 164.)...
Emkapon . [Emkay] Amide sulfonates det ent, dyeing assistant, scouring and wetting agoit, emulsifier to textile industry. [Pg.128]

Amides. Sulfonates of this type have been used as coupling reagents for formation of peptides. The by-products, being acidic, are readily removed by... [Pg.106]

Boiling amide amide sulfon Piccate point. of nitro ... [Pg.335]

No Name Melting point c S-Benzyl thiuro nium salt p Tolui dinium salt Ani- linium salt o Tolui dinium salt Sulfonyl chloride Sulfon- amide Sulfon- anilide Sulfon- l-naph- thylamide Miscellaneous... [Pg.371]

No Name Melting point, S Benzyl thiuro /7-ToIui dinium Am Imium o-Tolui dinium Sulfonyl chloride Sulfon- amide Sulfon anilide Sulfon 1 naph- Miscellaneous... [Pg.373]

No Name Meliing point, C S-Benzyl thiuro mum sail p Tolui dinium salt Am linium salt o Tolui dmmm salt Sulfonyl chloride Sulfon amide Sulfon- anilide Sulfon- 1-naph- ihylamide Miscellaneous... [Pg.374]

The functional group tolerance of this reaction is illustrated by olefins containing ester, amide, sulfone, and nitrile groups which can be applied to RhCl(PPh3)3-catalyzed orthoalkylation with remarkable efficiency (eq 68). These functionalized olefins are much more reactive than nonfunctionaUzed olefins. Nevertheless, when rhodium cationic species are employed as a catalyst, much higher yields of orthoalkylated products can be obtained under mild reaction conditions. [Pg.129]

Oxidation of Primary Alcohols. Primary alcohols can be oxidized in the presence of a variety of functional groups, including tetrahydropyranyl ethers (eq 1), epoxides (eq 2), acetals (eq 3), silyl ethers, peroxides, lactones, alkenes, alkynes, esters, amides, sulfones, and indoles. Oxidation of substrates with labile a-centers proceeds without epimerization. ... [Pg.476]

No Name Melting point c S-Benzyl thmro mum salt p>Tolui> diRium salt Am linium It o Tolui-dinium sah SuUonyl chloride Sulfori amide Sulfon anilide Sulfon l>naph- thyUmide Misodlaneous... [Pg.371]

No Name Mehing point. C S-Benxyl thiuro mum salt p Tolui dimum salt Am limum sab o-Tolui dimum sab SuiftNiyI dilonde Sulfon amide Sulfon- amlide Suifon- iHiaph- Uiylamide Miscellaneous... [Pg.374]

No Name Melting point, c S-Benzyl thiuro- mum salt Tolui dmium salt Am Iinium salt 0 Tolui-dimum salt Sulfonyt chloride Sulfon amide Sulfon- anilide Sulfon-1 naph-thylamide Miscellaneous... [Pg.376]

M. Bruma, F. Mercer, J. Fitch, P. Cassidy, Synthesis and characterization of fluorinated poly(imide-amide-sulfone)s, J. Appl. Polym. Sci. 56 (5) (1995) 527-532. [Pg.179]

The introduction of flexible bonds (e.g., -0-, -SO2-, etc.) helps to make the PAs soluble. Depending on the presence of different flexible spacers or fluorinated groups, PAs can be classified into three broad groups (1) normal fluorinated PA (2) fluorinated poly(ether amide)s containing flexible ether linkage (-0-) and (3) fluorinated poly(ether amide sulfone)s containing both the flexible ether and sulfone (-SO2-) linkages. [Pg.191]

Poly(ether amide sulfone)s contain two flexible groups, that is, ether (-0-) and sulfone (-SO2-). Liu et al. synthesized a new diamine containing pyridine moiety and-CF3groups,4-(4-trifluoromethylphenyl)-2,6-fcw(4-aminophenyl)pyridine, and used it for the preparation of PAs containing sulfone moieties (Figure 4.25) [23]. All these PAs showed good solubility... [Pg.207]


See other pages where Amides sulfonated is mentioned: [Pg.114]    [Pg.610]    [Pg.138]    [Pg.1686]    [Pg.1326]    [Pg.187]    [Pg.207]    [Pg.208]    [Pg.660]    [Pg.661]    [Pg.7]    [Pg.248]   
See also in sourсe #XX -- [ Pg.14 ]




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Amide sulfon

Amide sulfon

Amide, urethane, urea, and sulfonic acid

Amides sulfonate esters

Amine oxides sulfonic acid amides

Amines sulfonic acid amides

Benzene sulfonic amide

Hydroxylamines sulfonic acid amides

Sulfimides sulfonic acid amides

Sulfinic acid amides sulfones

Sulfonamides s. Sulfonic acid amides

Sulfonic acid a-alkoxyalkyl amides

Sulfonic acid amides

Sulfonic acid amides Sulfonylamin

Sulfonic acid amides Sulfonylamines)

Sulfonic acid amides anhydrides

Sulfonic acid amides arenes

Sulfonic acid amides aryl sulfones

Sulfonic acid amides azides

Sulfonic acid amides chlorides

Sulfonic acid amides disulfides

Sulfonic acid amides esters

Sulfonic acid amides fluorides

Sulfonic acid amides halides

Sulfonic acid amides heterocyclics

Sulfonic acid amides hydrazides

Sulfonic acid amides hydrocarbons

Sulfonic acid amides mercaptans

Sulfonic acid amides metal sulfonates

Sulfonic acid amides phenols

Sulfonic acid amides s. a. Sulfamyl

Sulfonic acid amides s.a. N-Sulfonyl

Sulfonic acid amides sulfinic acids

Sulfonic acid amides sulfonates

Sulfonic acid amides sulfones

Sulfonic acid amides sulfonylurethans

Sulfonic acid amides urethans

Sulfonylamines s. a. Sulfonic acid amides

Toluene sulfonic amide

Vinylation sulfonic acid amides

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