5441-60-1 Usage
General Description
N-methyl-1-(2-nitrophenyl)methanamine is a chemical compound that belongs to the class of aromatic amines. It is a derivative of nitrobenzene with a methyl substituent on the amino group. N-methyl-1-(2-nitrophenyl)methanamine has potential applications in pharmaceutical and chemical industries, particularly in the synthesis of organic compounds. It may also have uses in the development of new drugs and materials due to its unique structure and reactivity. However, it is important to handle this chemical with care and adhere to safety guidelines, as it is considered hazardous and could pose health risks if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 5441-60-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5441-60:
(6*5)+(5*4)+(4*4)+(3*1)+(2*6)+(1*0)=81
81 % 10 = 1
So 5441-60-1 is a valid CAS Registry Number.
5441-60-1Relevant articles and documents
Microwave-assisted synthesis of KN-93, a potent and selective inhibitor of Ca2+/calmoduline-dependent protein kinase II
Bruno, Claudio,Lentini, Giovanni,Catalano, Alessia,Carocci, Alessia,Lovece, Angelo,Di Mola, Antonia,Cavalluzzi, Maria Maddalena,Tortorella, Paolo,Loiodice, Fulvio,Iaccarino, Guido,Campiglia, Pietro,Novellino, Ettore,Franchini, Carlo
experimental part, p. 4193 - 4198 (2011/02/22)
Convenient synthetic routes to KN-93, N-(2-{[[(2E)-3-(4-chlorophenyl)prop- 2-enyl](methyl)amino]methyl}phenyl)-N-(2-hydroxyethyl)-4- methoxybenzenesulfonamide, a well-known Ca2+/calmoduline-dependent protein kinase II (CaMKII) inhibitor, are de
A Convenient Preparation of 3-Methyl-3,4-dihydro-2(1H)-quinazolinone
Golec, Frederick A.,Reilly, Laurence W.
, p. 789 - 790 (2007/10/02)
3-Methyl-3,4-dihydro-2(1H)-quinazolinone (5) can be prepared in good yield and quality from o-nitrobenzyl chloride (1).The three-step sequence requires no purification of intermediates or final product.
