67466-26-6 Usage
Uses
Used in Pharmaceutical Industry:
(4-OXO-6-PHENYL-1,4-DIHYDRO-PYRIMIDIN-2-YL-SULFANYL)-ACETIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential role in drug development. Its heterocyclic structure and functional groups contribute to its versatility in medicinal chemistry, allowing for the creation of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (4-OXO-6-PHENYL-1,4-DIHYDRO-PYRIMIDIN-2-YL-SULFANYL)-ACETIC ACID is utilized as a building block for the development of novel agrochemicals. Its unique properties may contribute to the creation of effective pesticides, herbicides, or other agricultural chemicals that can enhance crop protection and yield.
Used in Materials Science:
(4-OXO-6-PHENYL-1,4-DIHYDRO-PYRIMIDIN-2-YL-SULFANYL)-ACETIC ACID is employed in materials science for the development of new materials with specific properties. Its heterocyclic nature and functional groups can be leveraged to create materials with applications in various fields, such as electronics, coatings, or advanced materials for specific industries.
Check Digit Verification of cas no
The CAS Registry Mumber 67466-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,6 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67466-26:
(7*6)+(6*7)+(5*4)+(4*6)+(3*6)+(2*2)+(1*6)=156
156 % 10 = 6
So 67466-26-6 is a valid CAS Registry Number.
67466-26-6Relevant academic research and scientific papers
Attaby, Fawzy A.,Eldin, Sanaa M.
, p. 788 - 798 (1999)
Pyrimidin-4-one-2-thione (3) was synthesized via the reaction of thiourea (1) with ethyl henzoylacetate (2) and was taken as a starting material for the present study via its reactions with the halogen-containing reagents 6a-d and 10a-c to give the corresponding thiazolopyrimidines 8, 9 and 12a-c. The 2-hydrazino derivatives 5 were synthesized either via the reaction of 3 or 4 with hydrazine hydrate. Compound 5 reacted with 6a-c and 10a-c to give the corresponding pyrimidotriazines 17a-c and 19 respectively. Also, compound 5 reacted with the active methylene-containing reagents 13 and 2a,b to give the corresponding 2-pyrazolopyrimidines 15 and 22a,b respectively. On the other hand, the triazolopyrimidines 21a,b and 30a,b were also obtained via the reaction of 5 with each of formic acid, acetic anhydride, ethyl chloroformate and carbon disulfide respectively. Some of the newly synthesized heterocyclic derivatives were tested for their biological activity.
