89581-61-3 Usage
Uses
Used in Pharmaceutical and Drug Design:
CHEMBRDG-BB 4000145 is used as a chemical compound in the pharmaceutical and drug design industry for its potential biological activity, which could contribute to the development of new medications.
Used in Organic Synthesis:
CHEMBRDG-BB 4000145 is used as a chemical compound in organic synthesis for its unique structure and properties, which may contribute to the creation of new organic compounds.
Used in Material Science:
CHEMBRDG-BB 4000145 is used as a chemical compound in material science for its unique structure and properties, which may contribute to the development of new materials.
Check Digit Verification of cas no
The CAS Registry Mumber 89581-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,8 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89581-61:
(7*8)+(6*9)+(5*5)+(4*8)+(3*1)+(2*6)+(1*1)=183
183 % 10 = 3
So 89581-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClN2O3/c7-4-1-2-5(10)9(8-4)3-6(11)12/h1-2H,3H2,(H,11,12)
89581-61-3Relevant academic research and scientific papers
NOVEL PYRIDAZONES AND TRIAZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION
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Page/Page column 83-84, (2016/02/29)
The invention provides novel compounds having the general formula wherein R1, R2, R3, X and a are as described in the description and in the claims, as well as or pharmaceutically acceptable salts thereof. The invention also contains compositions including the compounds and methods of using the compounds.
Structure-activity relationships in a series of 8-substituted xanthines as A1-adenosine receptor antagonists
Strappaghetti, Giovannella,Corsano, Stefano,Barbaro, Roberta,Giannaccini, Gino,Betti, Laura
, p. 575 - 583 (2007/10/03)
A series of 8-substituted xanthines were synthesized and their affinity in vitro towards A1, A2A-adenosine receptors was evaluated by radioligand receptor binding assays. All compounds showed a greater affinity and selectivity toward
