6964-02-9 Usage
Uses
Used in Organic Synthesis:
N-(2-Methoxy-5-Methylphenyl)benzenesulfonaMide, 97% is used as a reagent in organic synthesis for its stability and versatility in chemical reactions. It can be employed in various research and industrial applications to facilitate the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(2-Methoxy-5-Methylphenyl)benzenesulfonaMide, 97% is used as an intermediate in the synthesis of various drugs. Its unique chemical structure allows it to be a key component in the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Research:
N-(2-Methoxy-5-Methylphenyl)benzenesulfonaMide, 97% is also used in chemical research to study the properties and reactions of sulfonamide derivatives. Its high purity and stability make it an ideal candidate for investigating the behavior of similar compounds in various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 6964-02-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6964-02:
(6*6)+(5*9)+(4*6)+(3*4)+(2*0)+(1*2)=119
119 % 10 = 9
So 6964-02-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3S/c1-11-8-9-14(18-2)13(10-11)15-19(16,17)12-6-4-3-5-7-12/h3-10,15H,1-2H3
6964-02-9Relevant articles and documents
One-pot ortho-amination of aryl C-H bonds using consecutive iron and copper catalysis
Henry, Martyn C.,McGrory, Rochelle,Faggyas, Réka J.,Mostafa, Mohamed A. B.,Sutherland, Andrew
, p. 4629 - 4639 (2019)
A one-pot approach for ortho-coupling of arenes with non-actived N-nucleophiles has been developed using sequential iron and copper catalysis. Regioselective ortho-activation of anisoles, anilines and phenols was achieved through iron(iii) triflimide catalysed iodination, followed by a copper(i)-catalysed, ligand-assisted coupling reaction with N-heterocycle, amide and sulfonamide-based nucleophiles. The synthetic utility of this one-pot, two-step method for the direct amination of ortho-aryl C-H bonds was demonstrated with the late-stage functionalisation of 3,4-dihydroquinolin-2-ones. This allowed the preparation of a TRIM24 bromodomain inhibitor and a series of novel analogues.
