132124-82-4 Usage
General Description
The chemical "2,4(1H,3H)-Pyrimidinedione, 6-amino-1,3-dimethyl-5-[(phenylimino)methyl]-" is a compound with a pyrimidine ring structure and an attached amino and methyl group. It also contains a phenylimino group. Pyrimidinedione compounds are a class of organic compounds that are widely used in the pharmaceutical and agricultural industries. The specific structure of this compound suggests potential applications in drug development and as a building block in organic synthesis. The amino and methyl groups can also contribute to the compound's reactivity and potential biological activity. Meanwhile, the presence of the phenylimino group suggests potential interactions with other biological molecules or receptors. Further research and investigation are needed to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 132124-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132124-82:
(8*1)+(7*3)+(6*2)+(5*1)+(4*2)+(3*4)+(2*8)+(1*2)=84
84 % 10 = 4
So 132124-82-4 is a valid CAS Registry Number.
132124-82-4Relevant articles and documents
Reactivities of 6-amino-1,3-dimethyl-5-thioformyluracil toward nucleophiles and its application to synthesis of pyrido[2,3-d]pyrimidines
Hirota, Kosaku,Kubo, Keiko,Sajiki, Hironao
, p. 542 - 544 (1997)
The reaction of the 5-thioformyluracil 1 with phenylhydrazine and various amines readily afforded the hydrazone 3a and Schiff bases 3b-d, respectively. Further, carbanions and Wittig reagents reacted with 1 to give pyrido[2,3-d]pyrimidines 4 and 9. The co
Iminophosphorane-mediated synthesis of fused uracils. A facile one-pot preparation of pyrimido[4,5-d]pyrimidine derivatives
Molina,Vilaplana,Perez
, p. 7855 - 7864 (2007/10/02)
The aza Wittig-type reaction of iminophosphoranes 3, 5-[(N-Arylimino)methyl]-6- [(triphenylphosphoranylidene)amino]-1,3-dimethyl uracils, with aromatic isocyanates leads to the functionalized pyrimido[4,5-d]pyrimidines 4. Iminophosphoranes 5, prepared from 3 by selective reduction with sodium borohydride, undergo dihydropyrimido annelation by reaction with isocyanates to give 7-amino-6-aryl-1,3-dimethyl-1,2,3,4,5,6- hexahydropyrimido[4,5-d]pyrimidines 6.
