58728-64-6 Usage
Description
4-Amino-1-naphthalenecarbonitrile, also known as 4-Aminonaphthalonitrile, is an organic compound derived from naphthalene. It is characterized by its brown fluffy powder or fine needle-like appearance. Upon hydrolysis, it yields 4-amino-1-naphthoic acid, which has potential applications in various industries.
Uses
Used in Chemical Synthesis:
4-Amino-1-naphthalenecarbonitrile is used as a chemical intermediate for the synthesis of various compounds, including pharmaceuticals, dyes, and pigments. Its unique structure allows for further functionalization and modification, making it a versatile building block in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Amino-1-naphthalenecarbonitrile is used as a key component in the development of new drugs. Its ability to form various derivatives and complexes with other molecules makes it a valuable asset in the design and synthesis of novel therapeutic agents.
Used in Dye and Pigment Industry:
4-Amino-1-naphthalenecarbonitrile is utilized as a starting material for the production of dyes and pigments. Its chemical properties enable the creation of a wide range of colors and shades, making it an essential component in the formulation of various colorants for the textile, paint, and plastics industries.
Used in Research and Development:
In the field of research and development, 4-Amino-1-naphthalenecarbonitrile serves as a valuable compound for studying the properties and behavior of naphthalene-based compounds. Its reactivity and structural characteristics make it an ideal candidate for exploring new chemical reactions and understanding the underlying mechanisms involved.
Check Digit Verification of cas no
The CAS Registry Mumber 58728-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,2 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58728-64:
(7*5)+(6*8)+(5*7)+(4*2)+(3*8)+(2*6)+(1*4)=166
166 % 10 = 6
So 58728-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2/c12-7-8-5-6-11(13)10-4-2-1-3-9(8)10/h1-6H,13H2
58728-64-6Relevant articles and documents
Benzimidazole derivatives as well as preparation method and application thereof
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Paragraph 0148; 0151;0152, (2016/10/08)
The invention belongs to the field of medicine, and relates to preparation methods of a series of benzimidazole derivatives, pharmaceutical salts of the benzimidazole derivatives and a pharmaceutically acceptable prodrug, pharmaceutical composition containing the derivatives, as well as an application of the derivatives and the pharmaceutical composition in preparation of anti-gout drugs and treatment of related diseases.
The Photochemical Reactions of 9,10-Anthracenedicarbonitrile and 1,4-Naphthalenedicarbonitrile in Acetonitrile in the Presence of Bases
Freccero, Mauro,Mella, Mariella,Albini, Angelo
, p. 2115 - 2130 (2007/10/02)
Irradiation of 9,10-anthracenedicarbonitrile (DCA) in MeCN-MeOH or MeCN-H2O containing hydroxides or methoxides leads to 9-methylimino-10-anthracenecarbonitrile (isolated, but easily hydrolyzed to the corresponding amine).Minor products are polycyanated amines and 9-hydroxy-10-anthracenecarbonitrile.Irradiation in neat MeOH causes decyanation.In both cases the first step is reduction to DCA-*, which persists for hour under these conditions.Evidence for the mechanism leading from the radical anion to the observed products is supplied.The key steps are protonation to yield the radical DCAH* and addition of the latter to acetonitrile, or to better nucleophiles when these are present. 1,4-Naphthalenedicarbonitrile is similarly transformed to the 4-amino-1-carbonitrile.
