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Halogenation esters

The chemical resistance of PCTFE is good but not as good as that of PTFE. Under certain circumstances substances such as chlorosulphonic acid, molten caustic alkalis and molten alkali metal will adversely affect the material. Alcohols, acids, phenols and aliphatic hydrocarbons have little effect but certain aromatic hydrocarbons, esters, halogenated hydrocarbons and ethers may cause swelling at elevated temperatures. [Pg.375]

Solvents can be classified into three categories according to their polarity namely, polar protic, dipolar aprotic and non-polar. Most of the common solvents fall under one of following chemical classes Aliphatic hydrocarbons, aromatic hydrocarbons, alcohols, phenols, ethers, aldehydes, ketones, carboxylic acids, esters, halogen-substituted hydrocarbons, amines, nitriles, nitro-derivatives, amides and sulfur-containing solvents (Marcus, 1998). In certain cases a mixture of two or more solvents would perform better than a single solvent. [Pg.116]

In 1991, Goff et al reported synthesis and activity testing of monoquatemary imidazole derivatives with various substituents sueh as ether, silicone, nitrile, ester, halogen, nitro, sulfone or amino group (Goff et al, 1991). Published literature reveals that syntheses started from 1-methyl-imidazole (Figure 66.5). [Pg.1000]

Tetracosane Phenyl cyclohexane Benzophenone Methyl stearate Lindane (152.2) C24H50 (338.7) C12H16 (160.3) C13H10O (182.2) C19H38O2 (298.5) CgHgClg (290.8) Hydrocarbon Aromatic hydrocarbon Aromatic ketone Aliphatic ester Halogenated hydrocarbon Non-volatile, non-polar, solid Non-volatile, non-polar, liquid Non-volatile, polar, solid Non-volatile, polar, solid Non-volatile, medium-polar, solid Surrogate for limonene Hazardous compound, should be substituted... [Pg.211]

Other groups that exhibit this behavior include thiol, sulfide, alkoxy (RO ), ester, halogen, and phenyl. [Pg.111]

Formation of a Boronic Ester Halogen-Lithium Exchange... [Pg.168]

When using boranes, esters, halogen derivatives, nitriles, amides, and nitro compounds are inert [BF2, BK5, HCl, HIl, OKI, YPl], This makes possible the... [Pg.96]

A method122 for hydrolyzing benzylidene and isopropylidene acetals by means of 90% trifluoroacetic acid is recommended. The procedure is mild and rapid, and does not affect esters, halogens, sulfonates, or azides. [Pg.205]

Activated acyl donors such as vinyl esters, halogenated methyl or ethyl ester, oxime esters or carboxylic acid anhydrides are often preferred for acylation of alcohols. With vinyl esters, acylation is in general fast and quantitative, as the equilibrium is driven by the release of vinyl alcohol, which will spontaneously tautomerize to volatile acetaldehyde. Amine nucleophiles will typically react spontaneously with these acyl donors, which hence cannot be used for resolution of amines. Vinyl acetate and ethyl acetate are common reagents (and often also solvents) for enzymatic kinetic resolution of alcohols and amines, respectively [9],... [Pg.367]

METAPHOSPHORIC ACID (7664-38-2) A medium-strong acid. Violent reaction with strong bases. Violent reaction if water is added to concentrated acid. To dilute, always add acid to water heat will be generated. Reacts violently with solutions containing ammonia or bleach, azo compounds, epoxides, and other polymerizable compounds. Reacts, possibly violently, with amines, aldehydes, alkanolamines, alcohols, alkylene oxides, amides, ammonia, ammonium hydroxide, calcium oxide, cyanides, epichlorohydrin, esters, halogenated... [Pg.746]

Santidzer Phosphoric acid esters, halogenated organic compounds Monsanto Co., St. Louis, MO, U.S.A. [Pg.824]

It is worth noting that the addition of the Grignard reagents to pyridine IV-oxides in THF at low temperature (from —78 to —20 °C) and treatment with trifluoroacetic anhydride (TFAA) provide an efficient general procedme for the synthesis of substituted pyridines (Scheme 14). The method is compatible with a range of functional groups, such as esters, halogens, and nitriles [36]. [Pg.160]

Major applications of ion pair extraction are alkylations (mainly C-alkylations), synthesis of esters, halogen and pseudohalogen exchanges, oxidations and reductions . In these cases, it is obviously important to recover and recycle the quaternary salt. A number of methods to this end were proposed by Brandstrom. ... [Pg.163]

Phosphate esters Halogenated Pentabromodiphenyl oxide/phosphate ester mixtures Tris (chloropropyl) phosphate (TCPP) Tris (chloroethyl) phosphate (TCEP) Tridichloroisopropyl phosphate (TDCPP) Nonhalogenated Triaryl phosphates Alkyldiaryl phosphates Trialkyl phosphates... [Pg.269]

Commercial chemical fibers are combustible in nature, and improved FR properties must be considered in actual application. Most FR additives contain bromine (Br), chlorine (Cl), phosphorus (P), antimony, or aluminum. Among them, commonly used additives are additive brominated hydrocarbons and reactive brominated hydrocarbons, nonhalogenated phosphate esters, halogenated phosphate esters, trioxide antimony oxide, pentoxide antimony oxide and sodium derivatives, chlorinated hydrocarbons like chlorinated paraffin, and chlorinated cycloaUphatics. Others include chlorinated or brominated compounds, fluorinated compounds, magnesium carbonate, magnesium hydroxide, melamine, molybdenum compounds, silicone polymer, and zinc borate. Sometimes, polymers are chemically modified, and N, P, Cl, fluorine (F), silicon (Si), and Br elements can be introduced into the polymer main chain [49]. [Pg.61]


See other pages where Halogenation esters is mentioned: [Pg.118]    [Pg.2424]    [Pg.22]    [Pg.181]    [Pg.31]    [Pg.264]    [Pg.2424]    [Pg.1234]    [Pg.35]    [Pg.900]    [Pg.973]    [Pg.977]    [Pg.999]    [Pg.568]    [Pg.24]    [Pg.390]    [Pg.280]    [Pg.154]    [Pg.445]    [Pg.292]    [Pg.60]    [Pg.49]    [Pg.229]   
See also in sourсe #XX -- [ Pg.954 ]




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6-Keto esters, acylation halogenation

Boronic esters reaction with halogen

Carboxylic esters halogenation

Carboxylic esters reductive halogenation

Carboxylic esters, acylation halogenation

Cyclopentanecarboxylic acid, 2-oxoethyl ester halogenation

Enol esters halogenation

Enol esters, acylation halogenation

Esters a-halogen

Esters halogen-atom substituted

Esters halogenated

Esters halogenated

Esters halogenated hydrocarbons

Esters halogenated solvents

Esters, silicate halogenation

Halogenated Esters of Organic Acids

Halogenation Hantzsch ester

Halogens esters

Halogens esters

Keto esters halogenations

Of a halogenated carboxylic esters

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