Expl derivs

As an expl, it is less powerful and brisant than Picric Acid (Ref 6). It has been used for the prepn of the foil owing expl derivatives ... [Pg.130]

There are several expl derivs of this compd viz, Pyrazolidimethylenepicrylacetate. [Pg.774]

N,2,2,2,2, 2, 2 -Heptanitrodiethylamine. Designated as HOX, also called Bis-2,2,2-trinitroethyl-nitrazine or Bis(2,2,2-trinitroethyl)-nitrazine, abbr as BTNEN. It is listed as an expl deriv of Diethylamine in Vol 5, p D1224-R... [Pg.63]

Hydrcxyaminobenzene. See Aminophenol in Vol, pp A241-L to A244-R. Its expl derivs 1-Hydroxy-2-amino-4,6-dinitrobenzene or Picramic Acid and 1-Hydroxy-4-amino-2,6-dinitrobenzene or Isopicramic Acid are on pp A241-R A243-R... [Pg.230]

Anilinotrimethylolmethane and Derivatives in Vol 1, p A441. Its highly expl deriv, designated as Heptryl is on pp A441-R to A442-R... [Pg.243]

Ethanolaniline and Derivatives. See ANILINO-E.THANOL AND DERIVATIVES in Vo 1 of Encycl, pp A424 to A429. Its expl derivative 2-(2Jf, 4, 6 -T ri ni tro-N-n i trani lino)- ethanol Nitrate, described on p A425-L, is called j3-(2,4,6-Trinitrophenylnitramino)-ethyl Nitrate in Blatt, OSRD 2014(1944) and code named Pehtryl. Compare with Ethyltetryl, which is described under N-Ethylaniline or N-Ethyl-phenyiamine and Derivatives... [Pg.54]

A number of expls have been prepd from raw materials involving formaldehyde. Although most of the formaldehyde expls are prepd from formaldehyde derivatives, several expls can be prepd directly in one operation from formaldehyde or anhydrous formaldehyde, or its polymer, paraformaldehyde. Walker (Ref 38), in his book on formaldehyde, gives a brief description of expls derived from it. For convenience, we divide them into two groups — those obtained directly from formaldehyde and those from formaldehyde derivatives... [Pg.547]

No expl props or expl derivs were reported Refs 1) Beil, not found 2) ADL, Synthesis HE S, 3rd Rept (1953), p384 3) ADL, Syn-... [Pg.339]

Dr L.Deffet, Bruxelles private communication, March 10,1954 Alkenyl Aromatics of the general formula Ar. CH, CHa. C CH2, were prepd by reacting aruEliatic nyuiocarbons (at moderate temp and press) with 1,3 diolefins in the presence of a catalyst(such as boron trihalide satd with an organic carboxylic acid). The purified alkenyl aromatics can be nitrated to yield expl derivs... [Pg.128]

No expl derivs were found listed in the literature (See also Anilinotriazoles)... [Pg.249]

Although not expl by itself, 5-ATZ may serve as the starting material for the prepn of expl derivs such as the nitrate, nitramino-compd, di(tetra2olyl-5) N, N -hexazadiene, etc, some of which are described beiow... [Pg.259]

The chemical reactions of HA have been the subject of numerous investigations. It reacts with acids (Refs 17,21,26,33,37,45, 56,60,64,82,92 109), oxidizing agents (Refs 14,32 76), reducing agents (Ref 34), and it forms expl derivs such as azides (Refs 38, 39 44), tetrazoles(Refs 24,25,30,31,40 ... [Pg.539]

N 18.06% yel ndls, mp 108° readily sol in benz, chlf acet mod sol in ale insol in w was prepd by boiling picryl chloride in ale with 45% aq cyclohexylamine. Nitration yields a more expl deriv... [Pg.383]

Cycloparaffins may be nitrated to produce expl derivs. See also Cycloalkanes, Peroxide Derivatives... [Pg.385]

According to Sax (Ref 12) succinic acid has a min lethal dose for frogs of 2g/kg. It is used as a general purpose food additive and forms the expl derivatives shown below... [Pg.453]

Some addnl expl derivatives and salts of Guanylnitrosoaminoguanyltetrazine, other than those shown in Vol 6 are the derivatives and salts of a misnomer compd, Diazoaminoguani-dine or Aminoguanidinediazonium (Note For a brief explanation of this error in nomenclature see under Aminoguanidinediazonium Hydroxide in Vol 1, A210-R)... [Pg.600]

Many tetrazoles are low brisance expls, and those containing tetrazole rings linked to chains of nitrogen atoms, such as Tetrazole Azide (see below) or 1,6-Ditetrazolylhexadiene (Vol 7, H91-L R) are exceedingly sensitive to heat and impact. Probably Diazotetrazole (Vol 5, D1176-L) represents the extreme in expl properties because it explds even in dilute aq solns (as low as 2%) and at temps as low as 0U. The expl derivatives of tetrazole are presented below ... [Pg.609]

N 86.66%. No prepn can be found for this compd. However, its expl derivatives are listed below ... [Pg.609]

This heterocyclic structure is an unusual molecule, having an interesting mixt of aromatic-aliphatic properties. It is considered as an explosophoric of possible great use, however with less power than tetrazole. A representative group of the expl derivatives of thiophene are presented below... [Pg.713]

Thiotrithiazyl. The (NS)3S— radical derived from Tetrasulfur Tetranitride (see in Vol 8, N102-L to N103-L, entered as Sulfur Nitride ). Its monosubstituted expl derivatives are presented below ... [Pg.714]

The parent compd is used as the hydrochloride in the synthesis of expl derivs... [Pg.842]

Triazole expl derivatives are presented below alphabetically under each parent structure type Refs 1) Beil 26,11,13 (5) la) A. Andreocci, Ber 25,225 (1892) 1 b) G. Pellizzari,... [Pg.853]

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