91040-94-7 Usage
Uses
Used in Pharmaceutical Synthesis:
(6-acetylnaphthalen-2-yl)acetic acid is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug candidates. Its unique structure allows for the creation of a wide range of medicinal compounds with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, (6-acetylnaphthalen-2-yl)acetic acid is used as a key intermediate in the synthesis of various agrochemicals, including pesticides and herbicides. Its incorporation into these products can enhance their effectiveness and selectivity in agricultural applications.
Used in Material Science:
(6-acetylnaphthalen-2-yl)acetic acid is utilized as a component in the development of new materials and functionalized surfaces due to its reactive nature and potential for molecular modification. This can lead to advancements in areas such as coatings, adhesives, and other industrial materials.
Used in Organic Synthesis Research:
As a versatile organic compound, (6-acetylnaphthalen-2-yl)acetic acid is used in research for organic synthesis, allowing scientists to explore new reaction pathways and develop innovative synthetic methods for creating complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 91040-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,4 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91040-94:
(7*9)+(6*1)+(5*0)+(4*4)+(3*0)+(2*9)+(1*4)=107
107 % 10 = 7
So 91040-94-7 is a valid CAS Registry Number.
91040-94-7Relevant academic research and scientific papers
Synthesis, structure and pharmacological activity of acyl-2-naphthalene acetic acids and derivatives
Saint Martino Descours,Pacheco,Venco,Yavordios
, p. 5 - 9 (2007/10/02)
Acyl 2-naphthalene acetic derivatives are obtained by a Friedel and Crafts reaction from methyl 2-naphthalene acetate. Low polarity solvents permit selective acylation in the 5 and 8 position, polar solvents in position 6 and 7. The structure of these products is demonstrated by NMR spectra (250 MHz) studies. Unambiguous syntheses of several of them were performed. Acyl 2-naphthalene acetic derivatives show lower anti-inflammatory, analgesic and antipyretic activities in animals than their 1-naphthalene analogs.
