5398-30-1 Usage
Uses
Used in Research and Laboratory Settings:
1-(1,1-dimethyl-3-oxobutyl)-3-phenylthiourea is utilized as a reagent for testing and analysis, playing a crucial role in various research and laboratory applications.
Used in Pharmaceutical and Medicinal Chemistry:
1-(1,1-dimethyl-3-oxobutyl)-3-phenylthiourea is employed as a compound with potential therapeutic applications, particularly for its anti-tumor and anti-cancer properties. It is being studied for its role in the treatment of various diseases and its contribution to the development of new medications.
Used in the Development of Treatments for Specific Diseases:
1-(1,1-dimethyl-3-oxobutyl)-3-phenylthiourea is explored for its potential use in the treatment of different diseases, given its demonstrated biological activities and its importance in medicinal chemistry. 1-(1,1-dimethyl-3-oxobutyl)-3-phenylthiourea's versatility makes it a valuable candidate for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 5398-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5398-30:
(6*5)+(5*3)+(4*9)+(3*8)+(2*3)+(1*0)=111
111 % 10 = 1
So 5398-30-1 is a valid CAS Registry Number.
5398-30-1Relevant academic research and scientific papers
Synthesis of Heterocyclic Compounds via Enamines. Part 8. Acid-catalysed Transformations in 4,4,6-Trimethyl-1,4-Dihydropyrimidine-2(3H)-thione Derivatives and Related Compounds
Singh, Harjit,Singh, Paramjit
, p. 1013 - 1018 (2007/10/02)
1-Substituted 4,4,6-trimethyl-1,4-dihydropyrimidine-2(3H)-thiones (2) on heating in 11M-HCl at 100-110 deg C are converted into the corresponding 2-substituted-amino-4,6,6-trimethyl-6H-1,3-thiazines (4) and/or thioureas.But at 95-100 deg C, Dimroth rearrangement products, e.g. the corresponding 2-substituted-amino-4,4,6-trimethyl-4H-1,3-thiazenes (3) are formed.
