25404-20-0 Usage
Uses
Used in Pharmaceutical Industry:
N-(2,6-dimethylphenyl)propanamide is used as an intermediate in the synthesis of various pharmaceuticals for its potential role in the development of new drugs. Its unique chemical structure allows it to be a key component in the creation of molecules with therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, N-(2,6-dimethylphenyl)propanamide is utilized as an intermediate in the synthesis of various agrochemicals, contributing to the development of products that can enhance crop protection and yield.
Used in Research and Development:
N-(2,6-dimethylphenyl)propanamide is used in research and development for its potential application in the treatment of various diseases and disorders. Its study in scientific laboratories aids in understanding its properties and exploring its therapeutic potential, which could lead to new medical breakthroughs.
Check Digit Verification of cas no
The CAS Registry Mumber 25404-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,0 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25404-20:
(7*2)+(6*5)+(5*4)+(4*0)+(3*4)+(2*2)+(1*0)=80
80 % 10 = 0
So 25404-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO/c1-4-10(13)12-11-8(2)6-5-7-9(11)3/h5-7H,4H2,1-3H3,(H,12,13)
25404-20-0Relevant academic research and scientific papers
Rhodium-Catalyzed Addition of Organozinc Iodides to Carbon-11 Isocyanates
Fouad, Moustafa H.,Ismailani, Uzair S.,Mair, Braeden A.,Munch, Maxime,Rotstein, Benjamin H.
supporting information, p. 2746 - 2750 (2020/04/16)
Amides were prepared using rhodium-catalyzed coupling of organozinc iodides and carbon-11 (11C, t1/2 = 20.4 min) isocyanates. Nonradioactive isocyanates and sp3 or sp2 organozinc iodides generated amides in yields of 13%-87%. Incorporation of cyclotron-produced [11C]CO2 into 11C-amide products proceeded in yields of 5%-99%. The synthetic utility of the methodology was demonstrated through the isolation of [11C]N-(4-fluorophenyl)-4-methoxybenzamide ([11C]6g) with a molar activity of 267 GBq μmol-1 and 12% radiochemical yield in 21 min from the beginning of synthesis.
