49593-56-8 Usage
Chemical class
Heterocyclic compound
Explanation
The compound has a pyrimidine ring structure, which consists of both carbon and nitrogen atoms.
Explanation
It is derived from pyrimidinone, a simple heterocyclic compound with a pyrimidine ring.
Explanation
The compound has a methyl group attached to a phenyl ring, and a phenyl group attached to the pyrimidine ring.
Explanation
The methyl and phenyl groups are attached at the 6th and 4th positions of the pyrimidine ring, respectively.
Explanation
The compound's heterocyclic structure and substitution pattern may affect its biological activity and pharmacokinetic properties, making it a potential candidate for pharmaceutical development.
Explanation
More research and study are required to fully understand the potential uses and effects of this chemical in various applications.
Structure
Pyrimidinone derivative
Additional groups
Methyl and phenyl groups
Position of substitution
6-(4-methylphenyl) and 4-phenyl
Potential applications
Pharmaceutical
Need for further research
Biological activity and pharmacokinetic properties
Check Digit Verification of cas no
The CAS Registry Mumber 49593-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,9 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49593-56:
(7*4)+(6*9)+(5*5)+(4*9)+(3*3)+(2*5)+(1*6)=168
168 % 10 = 8
So 49593-56-8 is a valid CAS Registry Number.
49593-56-8Relevant academic research and scientific papers
Organosilane sulfonated graphene oxide in the Biginelli and Biginelli-like reactions
Safari, Javad,Gandomi-Ravandi, Soheila,Ashiri, Samira
, p. 512 - 520 (2016/01/12)
Organosilane sulfonated graphene oxides (SSi-GO) have been synthesized by a two-step procedure involving the grafting of graphene oxide (GO) using 3-chloropropyltriethoxysilane (CCPTES) and subsequent oxidation using sulfanilic acid. It has been shown tha
Reaction of α,β-Unsaturated Ketones with Urea. Synthesis and Spectral Properties of 2(1H)-Pyrimidinone Derivatives
Sabri, Salim S.,Hussein, Ahmad Q.,Al-Hajjar, Farouk H.
, p. 512 - 514 (2007/10/02)
1,3-Diaryl-2-propen-1-ones react with urea to give 4,6-diaryl-3,4-dihydropyrimidinones (IVa-g) that can be further oxidized to the corresponding dehydro analogues (Va-f).The latter compounds are also obtained via interaction of aroylphenylacetylenes with urea.Spectral data, supporting the suggested structures IV and V, are presented.
