1975-45-7 Usage
Derivative
Naphthalene carboxylic acid
A chemical compound derived from naphthalene carboxylic acid
Nitro group position
6th position
The nitro group is attached to the sixth carbon atom in the naphthalene ring
Applications
Production of dyes, pigments, and pharmaceuticals
Utilized as an intermediate compound in the synthesis of various dyes, pigments, and pharmaceutical products
Synthesis of other organic compounds
Agrochemicals and plastic additives
Serves as an intermediate in the production of agrochemicals and plastic additives
Medicinal chemistry potential
Anti-inflammatory and anti-cancer properties
6-nitroanthranilic acid has been studied for its potential to exhibit anti-inflammatory and anti-cancer effects, making it a compound of interest in the field of medicinal chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 1975-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1975-45:
(6*1)+(5*9)+(4*7)+(3*5)+(2*4)+(1*5)=107
107 % 10 = 7
So 1975-45-7 is a valid CAS Registry Number.
1975-45-7Relevant articles and documents
Dziewonski,Kahl
, p. 394,397 (1934)
Design and Syntheses of 1,6-Naphthalene Derivatives as Selective HCMV Protease Inhibitors
Gopalsamy, Ariamala,Lim, Kitae,Ellingboe, John W.,Mitsner, Boris,Nikitenko, Antonia,Upeslacis, Janis,Mansour, Tarek S.,Olson, Matthew W.,Bebernitz, Geraldine A.,Grinberg, Diane,Feld, Boris,Moy, Franklin J.,O'Connell, John
, p. 1893 - 1899 (2007/10/03)
Through high throughput screening of various libraries, substituted styryl naphthalene 6 was identified as an HCMV protease inhibitor. Optimization of various regions of the lead molecule using parallel synthesis resulted in 1,6-substituted naphthalenes 1
Synthesis and structure-activity study of protease inhibitors. II. Amino- and guanidino-substituted naphthoates and tetrahydronaphthoates
Nakayama,Okutome,Matsui,Kurumi,Sakurai,Aoyama,Fujii
, p. 3968 - 3980 (2007/10/02)
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