F Dimethylamine

Dimethylamine, (CH3)2NH, an amine hydrocarbon derivative, is a gas with an ammonia-like odor. It is a dangerous fire risk, with a flammable range of 2.8 to 14% in air. It is insoluble in water. The vapor density is 1.55, which is heavier than air. The boiling point is 44°F, and the ignition temperature is 806°F. Dimethylamine is an irritant, with a TLV of 10 ppm in air. The four-digit UN identification number is 1032. The NFPA 704 designation is health 3, flammability 4, and reactivity 0. The... 

Hexametbyipbospboric triamide (HMPA) [680-31-9] M 179.2, f 7.2°, b 68-70°/lmm, 235°/760mm, d 1.024, n 1.460. The industrial synthesis is usually by treatment of POCI3 with excess of dimethylamine in isopropyl ether. Impurities are water, dimethylamine and its hydrochloride. It is purified by refluxing over BaO or CaO at about 4mm pressure in an atmosphere of nitrogen for several hours, then distd from sodium at the same pressure. The middle fraction (b ca 90°) is collected, refluxed over sodium under reduced pressure under nitrogen and distd. It is kept in the dark under nitrogen, and stored in solid CO2. Can also be stored over 4A molecular sieves. 

Dimethylamine, reaction with phosphorus trichloride, 46, 42 f-Dimethylami nobenzaldehyde, conversion to 0,/9-dichloro- -dimethyl-aminostyrene, 46, 34 tn-Dimethylaminobenzoic acid, 47, 71 /5-Dimethylaminobenzoic acid, 47, 71 6.(Dimethylamino)fulvene, 47, 52 -Dimethylaminophenylacetic acid, 47, 71... 

Chlor-bis-[c -hexen-(3)-yl-(3)]-aus 3-Hexin und Chlor-boran 56 Chlor- -Diathylather 7, 54 Dichlor- -THF 7 Dicyclohexyl- 7, 52 Diisopino-campheyl- 7 Herstellung 52 f Disiamyl- 6 -Dimethylamin 9 2,3-Dimethyl-butyl-(2)- 6, 53 Organo- 544 f. 

By way of graphical example of the various algebraic and geometrical concepts that are introduced in this chapter, we will make use of a measurement table adapted from Walczak etal.[ ]. Table 31.2 describes 23 substituted chalcones in terms of eight chromatographic retention times. Chalcone molecules are constituted of two phenyl rings joined by a chain of three-carbon atoms which carries a double bond and a ketone function. Substitutions have been made on each of the phenyl rings at the para-positions with respect to the chain. The substituents are CFj, F, H, methyl, ethyl, i-propyl, t-butyl, methoxy, dimethylamine, phenyl and NO2. Not all combinations two-by-two of these substituents are represented in the... 

Fig. 3 Apparent reduction potentials of (22) vs. 1 /N (N number of double bonds), from CV measurements in dimethylamine/TBABr, r =-60 °C, V = 100 mVs-f...

Buckley LA, Morgan KT, Swenberg JA, et al The toxicity of dimethylamine in F-344 rats and B6C3F1 mice following a 1-year inhalation exposure. Fundam Appl Toxicol 5 341-352, 1985... 

Gross EA, Patterson DL, Morgan KT Effects of acute and chronic dimethylamine exposure on the nasal mucociliary apparatus of F-344 rats. Toxicol Appl Pharmacol 90 359-376, 1987... 

Enamines or imines can form pyridines by cyclization to a nitrile group, as shown in the production of compound (48). Alternatively, the nitrogen atpm of the nitrile can be made more nucleophilic by attack on the carbon atom by an external nucleophile. Ammonia causes cyclization of the dienamines (53) (77JHC1077) and (54) (78JAP(K)786878l) in both cases, elimination of the amine introduces the extra double bond. Dimethylamine or piperidine cause cyclization of l-cyano-2,5,5-trimethylhex-l-en-3-yne to the f-butyl-pyridine (55). There are a few other examples of the synthesis of bicyclic compounds from... 

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