P- aniline

SYNS p-AMINOBENZENEARSONIC ACID 4-AMINOBENZENEARSONIC ACID AMINO-PHENYLARSINE ACID p-AMINOPHENYLARSINE ACID p-AMINOPHENYLARSINIC ACID 4-AMINOPHENYLARSONIC ACID p-ANILINE-ARSONIC ACID ANTOXYLIC ACID p-ARSANIL-IC ACID 4-ARSANILIC ACID ATOXYLIC ACID... 

SYNS ALBEXAN ALBOSAL AMBESIDE p-.UIINOBENZENESULFAMIDE p-AMINO-BENZENESULFONAMIDE 4-AMINOBENZENE-SULFONAMIDE p-AMINOPHENYLSULFONAMIDE 4-AMINOPHENYLSULFONAMIDE p-ANILINE-SULFONAMIDE ANILINE-p-SULFONIC AMIDE ANTISTREPT BACTERAMID COLLOMIDE COLSULANYDE COPTICIDE DIPRON ESTREPTOCEDA F 1162 FOURNEAU 1162 GERISON GOMBARDOL LUSIL LYSOCOCCINE... 

H3O2N.C8H4.Na mw 162.19, N 34.55% yel leaflets, mp 40° explodes at higher temp. Horner Gross (Ref 2) report its prepn N,N-Dimethyl-p-aniline (13-6g)... 

Yang et al. [53] prepared a novel series of metal-containing poly(imide)s. Polymers of pyromellitic dianhydride with the zinc, strontium, lead, calcium and nickel salts of p-aniline sulfonic acid, were prepared and examined by C CPMAS NMR. There was little difference in the chemical shifts of the dianhydride carbons, compared with the chemical shifts of the poly(imide) with diaminodiphenyl methane. 

Data from Fujita et al. (31). The II values for all functional groups except for NO2 (phenols, anilines) are those based on benzene as the parent compound II values for NO2 (m-, p-phenols) and NO2 (m-, p-anilines) are based on phenol and aniline as the parent compounds. 

AB) r piperazine (P), aniline (A), and 3-aminopropyl-triethoxysilane (AS). Glass slides were treated with amine at room temperature usually by immersing the slides for 5 min. in an amine-absolute ethanol solution. After removing the glass slides from the amine solution, the... 

The limulus amoebocyte lysate (LAL) test with chromogenic substrate is faster than the gelation method, and it can be automated. The chromogenic substrate is attached to p-nitroaniline, that is released when reacted with the endotoxin-activated enzymes. The free p-aniline is read at 405 nm. 

A First Principles Calculations and Experimental Study of the Ground- and Excited-State Properties of Ladder 01igo(p-aniline)s. 

Due to the utility of the methods and the significance of the materials, the use of Pd-catalyzed fV-arylation reactions in oligoaniline and polyaniline synthesis has remained an active area of research [344, 345]. For example, in recent work Kulszewicz-Bajer and coworkers have employed Pd-catalyzed amination reactions for the synthesis of AT-aryl poly(w,-p-aniline) derivatives that can be oxidized to high-spin radical cations [346, 347]. The preparation of these materials was accomplished by coupling 1,3-dibromobenzene with A TV -diarylphenylenediamine derivatives (Eq. 65). Palladium-catalyzed A -arylation reactions have also been employed for the preparation of partially annulated poly(w-anilines) [348] and other triarylamine-derived polymers [349, 350]. 

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