Naphthy lamine

Acetyl-AT-metbyl-o toluidine. Acetyl-AT-metbyl-m-toluidine. Acetyl-AT-methyl-p-toluidine. Acetyl-A7-methyl-a-napbthylamine Acety 1-AT-metbyl- P-naphthy lamine... 

The presence of A-phenyl-1 -naphthy lamine as inhibitor considerably reduces the development of peroxide in the ether. 

The diazonium ion then reacts with a coupling reagent. This reagent is usually an aromatic compound with an electron-rich nucleus, rendering it susceptible to an electrophilic attack by the diazonium ion. A typical coupling reagent is 1-naphthy-lamine (OC-naphthylamine). The following reaction takes place (Eq. (9)) ... 

In a plant that manufactured P-naphthy-lamine and benzidine, a cohort of 639 male employees with exposure from 1938 or 1939 to 1965 was studied concentration of initial exposure, duration of exposure, and years of survival after the exposure are factors that affected the incidence of tumor formation." Thirty-five percent of all malignant neoplasms were of the... 

Acetyl-Af-methyl-1 -naphthy lamine 94 Ethylisopropylbarbituric acid 201... 

Problem 18.53 Synthesize from benzene, toluene, naphthalene (NpH), and any aliphatic or inorganic compounds (a) a-(p-nitrophenyl)ethylamine, (b) / -(p-bromophenyl)ethylamine, (c) l-(a-aminomethyl)naphthalene, id) 2-naphthy-lamine, (e) /J-NpCH2NH2. ... 

The discovery of the temperature dependence of the photochemistry of phenyl azide prompted Leyva and Platz [85] to reexamine the photochemistry of 1-naphthyl azide. As mentioned previously photolysis of 1-naphthyl azide at 298 K in the presence of diethylamine fails to produce an azepine adduct, instead only a trace of diamine 9 is observed along with small amounts of azonaphthalene [51, 57, 91], The major product is 1-naphthy-lamine. Carroll et al. [51] improved the yield of diamine adduct with piperidine by adding N, N, N, N tetramethylethylenediamine (TMEDA) to complex with singlet 1-naphthyl nitrene. TMEDA did not improve the yield of diethylamine adduct, however. 

The reaction of long-chain vanilyl ester aldehydes with 2-naphthy-lamine and 1 afforded the benzo[c] acridines 395 (04MIb79,... 

Sample preparation 1 mL 5 mM Ibuprofen in dichloromethane + 300 jxL 1 mg/mL hy-droxybenzotriazole in dichloromethane pyridine 99 1 + 300 pL 11 mg/mL l-ethyl-3-di-methylaminopropylcarbodiimide in dichloromethane + 300 pL 3.47 mg/mL 1-naphthy-lamine (Caution 1-Naphthylamine in a carcinogen ) in dichloromethane, vortex, let stand for 1 h, evaporate to dryness under a stream of nitrogen, reconstitute with 5 mL MeOH, ii ject an aliquot. 

N-Phenyl-yS-naphthylamine (N -phenyl-2-naphthy-lamine, yS-naphthyl phenylamine, 2-anilino naphthalene) [135-88-6]... 

A-Phenyl-a-naphthylamine (A-phenyl-1 -naphthy-lamine, a-naphthyl phenylamine, 1-anilino naphthalene) [90-30-2]... 

Congo red [3,3 -4,4 -biphenylenebis(azo)bis(4-amino)-l-naphthalenesulfonic acid disodium salt, sodium diphenyldizao bis(a-naphthy-lamine sulfonate), benzo Congo red, direct red 28, Cl 22120] [573-58-0]... 

Radomaski, J.L. and Harrow, L.S., The metabolism of l-(o-talylazo)-2-naphthy-lamine (Yellow OB) in... 

Cascade intermolecular carbopalladations of alkynes followed by intramolecular trapping with electrophiles represent not only a novel type of organic transformation involving vinylpalladium intermediates, but also provide synthetically useful routes toward differently substituted indenols, indanones, indenones, and naphthy-lamines." Although these protocols are restricted to the intramolecular trapping with electrophiles, a wide application of this methodology toward the synthesis of various types of complex carbocychc compounds may be anticipated in the near future. 

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