35404-83-2 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dibromo-1,3-diphenylis used as a precursor in the synthesis of pharmaceuticals. Its unique structure allows for the creation of various drug molecules, contributing to the development of new medications.
Used in Agrochemical Production:
This chemical is also employed in the manufacture of agrochemicals, where it serves as an intermediate in the production of pesticides and other agricultural products. Its role in this industry is crucial for the development of effective and safe agrochemicals.
Used in Organic Synthesis:
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dibromo-1,3-diphenylis utilized as an intermediate in organic synthesis, enabling the creation of a wide range of organic compounds for various applications.
Used in Material Science:
In the field of material science, 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dibromo-1,3-diphenylis used for research purposes. Its properties and reactivity are studied to understand its potential applications in the development of new materials and technologies.
Used in Research:
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dibromo-1,3-diphenylis also used in research settings, where scientists explore its chemical properties, reactivity, and potential applications in various fields, including chemistry, biology, and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 35404-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,0 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35404-83:
(7*3)+(6*5)+(5*4)+(4*0)+(3*4)+(2*8)+(1*3)=102
102 % 10 = 2
So 35404-83-2 is a valid CAS Registry Number.
35404-83-2Relevant academic research and scientific papers
Synthesis of novel galactopyranosyl-derived spiro barbiturates
Ingle,Gaidhane,Dutta,Naha,Sengupta
, p. 661 - 671 (2007/10/03)
Malonic acid undergoes condensation readily with ureas to yield barbituric acids 2, which on bromination give 5,5-dibromobarbituric acids 3. Reaction of α-D-galactose with these 5,5-dibromo barbituric acids afforded 2,3-α-D-galactopyrano-1,4-dioxo-7,9-diaza-spiro[4,5]deca-6,8,10-triones 4. The structures of the products have been assigned on the basis of 1H NMR, 13C NMR, FAB-MS, optical activity, and elemental analysis. The title compounds are found to have antibacterial and antifungal activities.
