50350-45-3 Usage
Chemical class
Heterocyclic compound
Structure
Thiadiazole ring with an amine group (-NH2) at position 2, an ethyl group (-CH2CH3) and a methyl group (-CH3) attached to the nitrogen atom
Functional groups
Amine (-NH2), Ethyl (-CH2CH3), Methyl (-CH3)
Applications
Pharmaceutical and agrochemical research
Use
Building block for the synthesis of bioactive molecules, potential drug candidates, and crop protection agents
Synthetic utility
Diverse synthetic applications due to its chemical structure and functional groups
Importance
Key intermediate in the development of new compounds with biological activity
Check Digit Verification of cas no
The CAS Registry Mumber 50350-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,5 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50350-45:
(7*5)+(6*0)+(5*3)+(4*5)+(3*0)+(2*4)+(1*5)=83
83 % 10 = 3
So 50350-45-3 is a valid CAS Registry Number.
50350-45-3Relevant academic research and scientific papers
Mesoionic purinone analogs. 7. In vitro antibacterial activity of mesoionic 1,3,4 thiadiazolo[3,2 a]pyrimidine 5,7 diones
Coburn,Glennon,Chmielewicz
, p. 1025 - 1027 (2007/10/04)
The discovery of in vitro antibacterial activity of mesoionic thiazolo[3,2-αDpyrimidine-5,7-diones and mesoionic 1,3,4-thiadiazolo[3,2-α]pyrimidine-5,7-diones has been recently reported. These compounds are members of a large, virtually unknown, class of mesoionic structures, termed mesoionic purinone analogs, which are isoelectronic and isosteric to the purinones: xanthine, hypoxanthine, or purin-2-one. The formulation, classification, and quantum chemical study of a large number of these heterocyclic structures have been described. A series of alkyl and aryl substituted mesoionic 1,3,4-thiadiazolo[3,2-α]pyrimidine-5,7-diones, mesoionic xanthine analogs, was prepared and examined for antibacterial activity in order to develop structure activity relationships leading to more active derivatives.
