938-25-0

Usage

Uses

Used in Analytical Chemistry:
1,2-DiaMinonaphthalene is used as a fluorometric labeling reagent for the detection and quantification of specific compounds. Its ability to react with aldehydes and form fluorescent imidazole derivatives makes it a useful tool in this field.
Used in Biochemistry:
In biochemistry, 1,2-DiaMinonaphthalene is used for the fluorophotometric determination of selenium in certain types of mushrooms. This application takes advantage of its reactivity with aldehydes to produce fluorescent products, which can be measured to determine the presence and concentration of selenium.
Used in Research and Development:
Due to its unique chemical properties, 1,2-DiaMinonaphthalene is also utilized in research and development for the synthesis of new compounds and the investigation of various chemical reactions. Its ability to form fluorescent imidazole derivatives can be harnessed to develop new methods for detecting and analyzing biologically relevant molecules.

InChI:InChI=1/C10H10N2/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6H,11-12H2

Upstream product

• 10146-04-0 1-p-Tolylazo-naphthalen-2-ylamine 
• 10148-16-0 1-(4'-methoxybenzeneazo)-2-amino-naphthalene 
• 64-17-5 ethanol 
• 85-84-7 1-phenylazo-2-naphthylamine 
• 64-19-7 acetic acid 
• 56-23-5 tetrachloromethane 
• 14955-36-3 1-[2]naphthylazo-[2]naphthylamine 
• 52458-03-4 1-(2,4-dimethylphenylazo)-2-aminonaphthalene 
• 59823-87-9 1-[1]naphthylazo-[2]naphthylamine 
• 7647-01-0 hydrogenchloride 
• 19910-50-0 4-(2-amino-[1]naphthylazo)-benzenesulfonic acid 
• 134-32-7 1-amino-naphthalene 
• 618-40-6 1-Methyl-1-phenylhydrazine 
• 91-59-8 naphthalen-2-ylamine 

Downstream Products

• 861589-85-7 N-(1-amino-[2]naphthyl)-phthalamic acid 
• 5157-23-3 1,2-bis-(1(3)H-naphth[1,2-d]imidazol-2-yl)-benzene 
• 38515-17-2 N-(2-amino-[1]naphthyl)-benzamide 
• 233-68-1 naphtho{2,1-d}-2,1,3-thiadiazole 
• 10322-25-5 2,3-diphenyl-benzo[f]quinoxaline 
• 5649-75-2 1H-naphth<1,2-d>imidazol-2(3H)-one 
• 233-53-4 naphtho[1,2-d]imidazole 
• 94785-93-0 1⁽³⁾H-naphth[1,2-d]imidazol-2-ylamine 
• 3659-76-5 2-phenyl-1(3)H-naphth[1,2-d]imidazole 

Relevant academic research and scientific papers

A new method for N-N bond cleavage of N,N-disubstituted hydrazines to secondary amines and direct ortho amination of naphthol and its analogues

An unexpected reaction of N,N-disubstituted hydrazine with naphthol and its analogues under simply thermal conditions has been disclosed. 2-Naphthol reacted with various N,N-disubstituted hydrazines under argon to afford 1-amino-2-naphthol and the corresponding secondary amines in excellent yields. Ortho amination of 2-naphthols, hydroxyquinoline, and naphthalenamine occurred when they reacted with N-methyl-N-phenylhydrazine. Copyright

Antiproliferative compounds having nitrogen-containing tricyclic ring systems and phenyl substituents

The invention relates to TS-inhibiting compounds of the formula STR1 where W is an alkylene group; D is a structure having two rings that are unsubstituted or substituted, where (i) one ring is a phenyl ring and (ii) the other ring is a phenyl ring or a 6