2924-95-0 Usage
General Description
N-(4-trifluoromethylphenyl)propionamide is a chemical compound with the molecular formula C10H10F3NO. It is a white to off-white crystalline powder that is soluble in organic solvents like dimethyl sulfoxide and acetone. N-(4-TRIFLUOROMETHYLPHENYL)PROPIONAMIDE is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It has also been studied for its potential use as an anti-inflammatory and analgesic agent. Additionally, N-(4-trifluoromethylphenyl)propionamide has been investigated for its antimicrobial and antifungal properties. As with any chemical compound, proper handling and storage guidelines should be followed to ensure safety and prevent any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 2924-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2924-95:
(6*2)+(5*9)+(4*2)+(3*4)+(2*9)+(1*5)=100
100 % 10 = 0
So 2924-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10F3NO/c1-2-9(15)14-8-5-3-7(4-6-8)10(11,12)13/h3-6H,2H2,1H3,(H,14,15)
2924-95-0Relevant articles and documents
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.
