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Basic group

The basic groups met in medicinal chemistry are the amines, the amidines, the guanidines and practically all nitrogen-containing heterocycles. Basic groups are polar and one [Pg.458]


Sephadex A trade name for an insoluble hydrophilic substance prepared by cross-linking dextran, and used in gel filtration. It can also be linked to acidic or basic groups for ion exchange or to alkanes for the chromatography of lipophilic compounds. [Pg.356]

Other Lewis basic groups can direct the hydrogenation. (Ir seems to be superior to Rh for these cases)... [Pg.34]

Some ammo acids have side chains that bear acidic or basic groups As Table 27 3 indicates these ammo acids are characterized by three values The third pK reflects the nature of the side chain Acidic ammo acids (aspartic and glutamic acid) have acidic side chains basic ammo acids (lysine arginine and histidine) have basic side chains The isoelectric points of the ammo acids m Table 27 3 are midway between the pK values of the zwitterion and its conjugate acid Take two examples aspartic acid and lysine Aspartic acid has an acidic side chain and a pi of 2 77 Lysine has a basic side chain and a pi of 9 74... [Pg.1118]

Descriptive properties for a basic group of inorganic compounds are compiled in Section 3, which has undergone a small increase in the number of entries. Many entries under the column Solubility supply the reader with precise quantities dissolved in a stated solvent and at a given temperature. [Pg.1283]

Descriptive properties for a basic group of approximately 1400 inorganic compounds are compiled in Section 3. These follow a concise, revised introduction to inorganic nomenclature that follows the recommendations of the lUPAC published in 1990. In this section are given the exact atomic (or formula) weight of the elements accompanied, when available, by the uncertainty in the final figure given in parentheses. [Pg.1286]

Albumen has the largest number of acid and basic groups. It is the most soluble of the proteins present in a hide. The albumen is not a fibrous material, however, and therefore has no value in the leather. Keratin is the protein of the hair and the outermost surface of the hide. Unless the hair is desired for the final product it is removed by chemical and/or physical means. The elastin has Htde acid- or base-binding capacity and is the least soluble of the proteins present. The lack of reactivity of the elastin is a detriment for most leather manufacture. The presence of elastin in the leather greatly limits the softness of the leather. [Pg.82]

The side groups of the amino acids vary markedly in size and chemical nature and play an important role in the chemical reactions of the fiber. For example, the basic groups (hisidine, arginine, and lysine) can attract acid (anionic) dyes, and in addition the side chains of lysine and hisidine are important sites for the attachment of reactive dyes. The sulfur-containing amino acid cysteine plays a very important role, because almost all of the cysteine residues in the fiber are linked in pairs to form cystine residues, which provide a disulfide bridge —S—S— between different polypeptide molecules or between segments of the same molecules as shown ... [Pg.343]

Other modifications of acid wool dyes have groups which react by nucleophilic substitution of basic groups ia proteia fibers (NH2 groups, etc). The iatroduction of Procion dyes by ICI ia 1956 was the most important development ia the field of technological azo dye chemistry. Chemically, many of the reactive dyes are prepared from the group of the anionic monoazo dyes (see Dyes, reactive). [Pg.436]

Carbonates undergo nucleophilic substitution reactions analogous to chloroformates except in this case, an OR group (rather than chloride) is replaced by a more basic group. Normally these reactions are cataly2ed by bases. Carbonates are sometimes preferred over chloroformates because formation of hydrogen chloride as a by-product is avoided, which simplifies handling. However, the reactivity of carbonates toward nucleophiles is considerably less than chloroformates. [Pg.43]

In sodium chloride solutions the ion transport number for Na+ is about 0.4 compared to about 0.6 for CU. Thus a CX membrane would be expected to polarize at lower current densities than an AX membrane. Careful measurements show that CX membranes do polarize at lower current densities however, the effects on pH are not as significant as those found when AX membranes polarize. Such differences ia behavior have beea satisfactorily explaiaed as resultiag from catalysis of water dissociatioa by weaMy basic groups ia the AX membrane surfaces and/or by weaMy acidic organic compounds absorbed on such surfaces (5). [Pg.174]

Modification of urea resins with certain organic bases, e.g. triethylene-tetramine, will give resins with basic groups which form ionisable salts in the presence of acids ... [Pg.680]

In the series NHR. CO. O. CgH. NMe all the members tried in which R is a methyl group were active, but when R is ethyl or hydrogen, miotic action is reduced or may even disappear, thus the p and m-dimethylaminophenyl esters of ethylcarbamic acid (R = C2H5) are inactive but the o-ester is active, indicating that activity is also influenced by the position and nature of the basic group. When the tertiary basic... [Pg.549]

The reactivity of the methyl group in 4-methylcinnoline ethiodide indicates that the structure of this compound is 5, and this evidence has also been interpreted to mean that N-1 is the basic group in cinnolines. However, evidence of this type is only indicative since the formation of quaternary salts is subject to kinetic control, whereas protonation yields predominantly the thermodynamically more stable cation. The quinazoline cation has been shown to exist in the hydrated, resonance-stabilized form 6 7 by ultraviolet spectro-... [Pg.341]

As noted previously, triarylethylenes substituted by a basic group, such as clomiphene, exhibit estrogen antagonist activity. Formal cyclization of that molecule to a more steroid-like, rigid conformation enhances potency in this series. [Pg.148]

Substitution of additional basic groups onto a closely related nucleus affords a compound with muscle relaxant activity with some activity in the treatment of angina. Reaction of the... [Pg.427]

The antiarrhythmic activity of local anesthetics has been noted several times previously. Another such agent is prepared by first alkylating isopropylamine with sulfone 199. Reaction of the ])ioduct (200) with diethylethylenediamine and carbonyldiimidazole results in transfer of the CDI carbonyl group and formation of the urea suricainide (201) [52]. The transform in all likelihood involves stepwise replacement of the imidazole groups by the basic groups in the other reactants. [Pg.49]

Physical property prediction in polymer science has evolved from the original basic group contribution meth-... [Pg.25]

Rotary pumps are classified in two basic groups and several subgroups. These are ... [Pg.469]

This falls into two basic groupings supply air systems and extract systems. The equipment used for both is similar, comprising, as a minimum, a fan and weatherproof cowl, plus ducting, air-treatment equipment and grilles as required. [Pg.423]

Cathodic-protection schemes utilising the impressed-current method fall into two basic groups, dictated by the anode material ... [Pg.208]

Crystallisation is often used as a method to recover tire amino add. Because of tire amphoteric character (contains both addic and basic groups) of amino adds, their solubility is greatly influenced by the pH of the solution and usually show minima at the isoelectric point (zero net charge). [Pg.250]


See other pages where Basic group is mentioned: [Pg.178]    [Pg.694]    [Pg.55]    [Pg.1283]    [Pg.1286]    [Pg.99]    [Pg.141]    [Pg.82]    [Pg.295]    [Pg.540]    [Pg.15]    [Pg.338]    [Pg.202]    [Pg.315]    [Pg.121]    [Pg.22]    [Pg.560]    [Pg.677]    [Pg.102]    [Pg.122]    [Pg.66]    [Pg.426]    [Pg.162]    [Pg.10]    [Pg.2]    [Pg.431]    [Pg.879]    [Pg.151]    [Pg.333]   
See also in sourсe #XX -- [ Pg.48 , Pg.59 , Pg.201 , Pg.234 ]

See also in sourсe #XX -- [ Pg.181 , Pg.182 , Pg.216 , Pg.243 , Pg.245 , Pg.253 , Pg.255 , Pg.274 , Pg.280 , Pg.390 , Pg.391 , Pg.454 ]

See also in sourсe #XX -- [ Pg.19 , Pg.59 ]




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Activated carbon basic groups

Amide group basicity

Amino acid residues, basic functional groups

Amino acids group 4- basic side chains

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Basic Facts from Group Theory

Basic OH group

Basic Point Group Theory

Basic Stereochemistry of the 1,4-Dioxa Group in Polyether Complexes

Basic Unit Hydroxyl Groups

Basic group parameters

Basic groups on protein

Basic groups, carbohydrates

Basicity Carbonate, oxide group

Basicity leaving groups

Basicity of functional groups

Basicity, concept groups

Basicity, silanol group

Basicity, silanol group activation

Basicity, silanol group water exchange

Bayer Basic and Fine Chemicals Business Group

Carbonyl group basicity

Carbonyl reduction Lewis basic functional groups

Carboxylate anion, basicity Carboxyl group

Containing Cationic Groups (Basic Dyes)

Cyano group, basicity

Functional groups basic

Functional groups: chemical identification basic compounds

Lewis basic groups

Lewis basic nitro group

Polymer groups basic

Protecting groups basic-labile

Substituents basic groups

Surface groups basic

The Role of Proximal, Lewis Basic Functional Groups in Carbonyl Reduction

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