57476-37-6 Usage
General Description
2,6-Dichloro-8-methyl-9H-purine, also known as 8-methyl-2,6-dichloro-9H-purine or 8-methyl-2,6-dichloropurine, is an organic compound belonging to the purine family. It is a derivative of purine, which is a heterocyclic aromatic organic compound that occurs widely in nature as part of various nucleic acids and is also a component of certain drugs and vitamins. This chemical is a white crystalline solid with a molecular formula C7H5Cl2N5 and a molecular weight of 219.056 g/mol. 2,6-Dichloro-8-methyl-9H-purine is used in the synthesis of pharmaceuticals and research chemicals and has potential applications in the fields of medicine and biotechnology. However, it is important to handle this compound with caution as it may pose hazards to health and the environment if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 57476-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57476-37:
(7*5)+(6*7)+(5*4)+(4*7)+(3*6)+(2*3)+(1*7)=156
156 % 10 = 6
So 57476-37-6 is a valid CAS Registry Number.
57476-37-6Relevant articles and documents
2,6,8,9-Tetrasubstituted purines as new CDK1 inhibitors
Moravec, Jiri,Krystof, Vladimir,Hanus, Jan,Havlicek, Libor,Moravcova, Daniela,Fuksova, Kvetoslava,Kuzma, Marek,Lenobel, Rene,Otyepka, Michal,Strnad, Miroslav
, p. 2993 - 2996 (2003)
Purine inhibitors of cyclin-dependent kinases attract attention as potential anticancer drugs because their first representative roscovitine recently entered clinical trials. Although well described in terms of structure-activity relationships, we still p
Regioselectivity in cross-coupling reactions of 2,6,8-trichloro-9- (tetrahydropyran-2-yl)purine: Synthesis of 2,6,8-trisubstituted purine bases
Hocek, Michal,Pohl, Radek
, p. 2869 - 2876 (2007/10/03)
The regioselectivity of cross-coupling reactions (Pd-catalyzed Suzuki-Miyaura reactions with phenylboronic acid and Fe-catalyzed reactions with methylmagnesium chloride) of 2,6,8-trichloro-9-(tetrahydropyran-2-yl)purine with varying amounts of the organom
