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N-Phenylnaphthalen-1-amine (NPN) is an aromatic amine with the chemical formula C 16 H 12 NH. This molecule is notable for its binding affinity in mouse major urinary ...
The molecular formula C 16 H 13 N (molar mass: 219.28 g/mol, exact mass: 219.1048 u) may refer to: Benzylisoquinoline; N-Phenylnaphthalen-1-amine (NPN)
reduction of 1-nitroonaphthalene-8-sulfonic acid, precursor to C.I. Acid Blue 113 Notes: Peri-acid dehydrates to the sultam . Via the Bucherer reaction , heating periacid with anilinium salts gives the N-phenyl derivative, precursor to Acid Blue 113.
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N-(1-Naphthyl)ethylenediamine dihydrochloride is widely used in the quantitative analysis of nitrate and nitrite in water samples by colorimetry.It readily undergoes a diazonium coupling reaction in the presence of nitrite to give a strongly colored azo compound.
The sulfonic acid derivatives of 1-naphthylamine are used for the preparation of azo dye.These compounds possess the important property of dyeing unmordanted cotton.. An important derivative is naphthionic acid (1-aminonaphthalene-4-sulfonic acid), which is produced by heating 1-naphthylamine and sulfuric acid to 170–180 °C in the presence of crystallized oxalic acid.
N,N-Dimethyl-1-naphthylamine is an aromatic amine. It is formally derived from 1-naphthylamine by replacing the hydrogen atoms on the amino group with methyl groups . N , N -Dimethyl-1-naphthylamine is used in the nitrate reductase test to form a precipitate of a red azo dye by reacting with a nitrite - sulfanilic acid complex.
1,8-Naphthalic anhydride is an organic compound with the formula C 10 H 6 (C 2 O 3). It is one of three isomers of naphthalic anhydride, the other two being the 1,2- and the 2,3-derivatives. The 1,8-isomer is prepared by aerobic oxidation of acenaphthene. [1] 2,6-naphthalenedicarboxylic acid can be prepared from this anhydride.