91040-96-9 Usage
Uses
Used in Organic Synthesis:
[6-(2-methylpropyl)naphthalen-2-yl]acetic acid is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [6-(2-methylpropyl)naphthalen-2-yl]acetic acid serves as a valuable compound for studying the structure-activity relationships of biological targets. Its potential biological and pharmacological activities make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
Medicinal chemists utilize [6-(2-methylpropyl)naphthalen-2-yl]acetic acid as a starting material or a building block for designing and synthesizing novel molecules with potential therapeutic properties. Its structure and properties facilitate the exploration of new drug candidates and contribute to the advancement of pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 91040-96-9 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 91040-96:
(7*9)+(6*1)+(5*0)+(4*4)+(3*0)+(2*9)+(1*6)=109
109 % 10 = 9
So 91040-96-9 is a valid CAS Registry Number.
91040-96-9Relevant 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.
