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Fuses and fusing

Systems of this type are still dominated by those containing a nitrogen atom, particularly with one or more rings fused to the seven-membered ring. The following material is divided into non-fused and fused examples. [Pg.341]

A number of interesting preparations and reactions have been described, although activity in this particular area has not been especially high. As was done previously, some of the following material is divided into non-fused and fused ring examples. [Pg.431]

Place blasting cap in the hole in top of the charge. If nonelectric cap is used, be sure cap is crimped around fuse and fuse is long enough to provide safe delay. [Pg.95]

The material in this chapter has been organised into ring-type and functional-group order so that required information may be rapidly obtained. Monocyclic systems and their alkyl derivatives are reviewed first, followed by related compounds, in order of their functional groups. This is followed by polycyclic systems (non-fused and fused). Derivatives of these are covered under the appropriate parent compound heading, appearing in the same order as that in the earlier sections. Later sections include more specialised systems such as helicenes and cyclophanes. Synthesis and reactivity are discussed collectively under the appropriate system heading. [Pg.91]

Dissolves in alkaline solutions to give purple-red solutions which are precipitated as lakes by heavy metal salts. Occurs naturally as a glucoside in madder but produced synthetically by fusing anthraquinone-2-sulphonic acid with NaOH and some KCIO3. Applied to the mordanted fibre. Al(OH)3 gives a bright red lake, Cr(OH)3 a red lake, FefOH) ... [Pg.20]

Prepared by reduction of 4-nitrophenol or 4-nitrosophenoi. Can be diazotized and used as a first component in azo-dyes. Chief outlet is for sulphur dyes in which it is fused with sodium polysulphides. L/sed as a photographic developer. [Pg.30]

Obtained by fusing o-t nzenedisulphonic acid with NaOH. It is used as a photographic developer, for preparation of dyes and pharmaceuticals, and as an antioxidant. [Pg.139]

It occurs in many natural glycosides. It can be prepared by fusing resorcinol with NaOH and is manufactured from trinitrotoluene via trinitrobenzoic acid and triaminobenzene. [Pg.306]

C, b.p. 205°C, forms monohydrate m.p. 58°C. Prepared from diacetoneamine and propanone or by passing NH3 gas into pro-panone containing fused CaCl2. Decomposes to phorone and ammonia, reduced to lelra-melhyl-3-hydroxypiperidine. Used in the synthesis of benzamine hydrochloride. [Pg.403]

Simple examples of WLN are C2H5OH is Q2 CH3C0 0CH3 is IVOl For branch chain and fused ring structures rules determine the order of notation. It is claimed that over 50% of all organic structures can be represented by less than 25 characters, witherite, BaCOj. The white mineral form of barium carbonate. Used as a source of Ba compounds and in the brick and ceramic industries. [Pg.426]

Figure III-9u shows some data for fairly ideal solutions [81] where the solid lines 2, 3, and 6 show the attempt to fit the data with Eq. III-53 line 4 by taking ff as a purely empirical constant and line 5, by the use of the Hildebrand-Scott equation [81]. As a further example of solution behavior, Fig. III-9b shows some data on fused-salt mixtures [83] the dotted lines show the fit to Eq. III-SS. Figure III-9u shows some data for fairly ideal solutions [81] where the solid lines 2, 3, and 6 show the attempt to fit the data with Eq. III-53 line 4 by taking ff as a purely empirical constant and line 5, by the use of the Hildebrand-Scott equation [81]. As a further example of solution behavior, Fig. III-9b shows some data on fused-salt mixtures [83] the dotted lines show the fit to Eq. III-SS.
Fig. VI-3. Attraction between fused-silica flat plates and spheres of radius 413.5 cm (I) or 83.75 cm (II). The lines are drawn with a slope of -3.00. (From Ref. 27.)... Fig. VI-3. Attraction between fused-silica flat plates and spheres of radius 413.5 cm (I) or 83.75 cm (II). The lines are drawn with a slope of -3.00. (From Ref. 27.)...

See other pages where Fuses and fusing is mentioned: [Pg.1108]    [Pg.15]    [Pg.17]    [Pg.24]    [Pg.26]    [Pg.42]    [Pg.44]    [Pg.48]    [Pg.60]    [Pg.66]    [Pg.75]    [Pg.135]    [Pg.157]    [Pg.190]    [Pg.197]    [Pg.199]    [Pg.213]    [Pg.241]    [Pg.245]    [Pg.246]    [Pg.264]    [Pg.275]    [Pg.278]    [Pg.317]    [Pg.345]    [Pg.348]    [Pg.348]    [Pg.358]    [Pg.362]    [Pg.366]    [Pg.374]    [Pg.385]    [Pg.385]    [Pg.408]    [Pg.409]    [Pg.413]    [Pg.414]    [Pg.416]    [Pg.543]    [Pg.67]    [Pg.257]    [Pg.729]    [Pg.1973]    [Pg.2417]   
See also in sourсe #XX -- [ Pg.154 , Pg.173 ]




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1.2.3- Triazoles and ring-fused derivatives

1.2.4- Triazines fused to heterocycles with 6-and 7-membered

Alternating Rings of Fused Benzene and Thiophene Molecules (ABTs)

And fused ring compounds

Aromatic Fused Dithiepines and Their -Oxides

Benzene-fused heterocycles containing tellurium, selenium and sulphur

Benzothiophens and their Benzo-fused Systems

Benzotriazoles and Higher Fused Systems

Bridged and Fused Rings

By Oxidation of Alkyl-, Styryl-, Hydroxyalkyl-, and Fused Pyrazine Systems

Circuit breakers and fuses

Compounds containing Fused Five- and Six-Membered Rings

Compounds containing Three or Four Fused Heterocyclic Rings (5,5,5), (5,5,6), (5,5,7), (5,6,7), and

Condensed 1,2,4-triazines: I. Fused heterocycles with three-, four-, and

Condensed 1,2,4-triazines: I. Fused heterocycles with three-, four-, and fivemembered rings

Cyclic and helical fused oligothiophenes

Diazepines and fused derivatives

Dioxepines, dithiepines and fused derivatives

Expanding and Fusing

FUSED-RING OXIRENES AND THIIRENES

Fischer, G., Tropones, Tropolones, and Tropylium Salts with Fused Heterocyclic

Five-Membered Heterocyclic Rings and Their Fused Derivatives

Formation of - and -Fused Systems

Fused Five and Six Ring Nitrogen Systems

Fused Five- and Six-Membered Rings

Fused Polycyclic and peri-Condensed Benzenoid Systems

Fused Pyrimidines Purines and Pteridines

Fused Quartz Channel Etching and Hole-Drilling

Fused Silica and Other Glasses

Fused and spirocyclic p-lactams

Fused aromatic compounds, and

Fused azepines and derivatives

Fused to heterocycles with 6-and

Fused to heterocycles with 6-and 7-membered rings

Fused-Ring Five-Membered Heterocycles Indoles and Purines

Fused-ring and Bicyclic Azasugars

Fusing rings to pyridines quinolines and isoquinolines

Geometrical and Chemical Structure of Fused Silica Surface

Halogenation fused to other aromatic and

Halogenation fused to other aromatic and heteroaromatic

Imidazoles and ring-fused derivatives

Metal halides in the fused and vapour states

Monomers containing a fused cyclopentene ring and more than one double bond

Myers-Saito and Schmittel) Routes to Indeno-Fused Structures

Other Fused Bicyclic 6-6 and 6-7 Rings

Oxazines and their Fused Derivatives

Oxazines, Thiazines, and their Fused Derivatives

Oxepine and fused derivatives

Oxepines and fused derivatives

Oxidation of Quinoxalines and Other Fused Pyrazines to Pyrazinecarboxylic Acids

PYRAZOLES, INDAZOLES, AND THEIR DERIVATIVES AS STARTING MATERIALS FOR THE SYNTHESES OF FUSED RING SYSTEMS

Polymer Fusing and Other Assembly Techniques

Primordial Fused Genes Become Oncogenes and Encode Oncoproteins

Pyrazole-, Thiazole-, and Imidazole-fused Thiophens

Pyrazoles and ring-fused derivatives

Pyrimidines and their Fused Ring Systems

Quartz and Fused Silica

Quinolinone (Pyridone), Coumarin, and Other Fused Ring SARMs

Reactions of thiazoles and fused derivatives

Saturated bicyclic 6/5 ring-fused systems with bridgehead nitrogen and a single

Saturated bicyclic 6/5 ring-fused systems with bridgehead nitrogen and a single additional

Synthesis and Polymerization of Fused Bicyclic Orthoesters

Synthesis of thiazoles and fused derivatives

Tetrahydropyridazines and Hydropyridazines with Fused Rings

Tetrazoles and ring-fused derivatives

Thiazines and their Fused Derivatives

Thiepine and fused derivatives

Thiepines and fused derivatives

Thiophen-fused Tropylium Ions and Related Compounds

Triazines, tetrazines and fused ring polyaza systems

Triazines, tetrazines, and fused polyaza-systems

Triazino and tetrazino fused systems

Tropolones with fused heterocyclic rings structure, reactivity, and application

Tropones with fused heterocyclic rings structure, reactivity, and application

Tropylium salts with fused hetercyclic rings structure, reactivity, and application

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