89939-20-8 Usage
Heterocyclic organic compound
2(1H)-Quinoxalinethione, 4-oxide is a compound that contains a ring structure with at least one heteroatom, which is an atom other than carbon, such as nitrogen or oxygen.
Commonly used in organic synthesis and medicinal chemistry
2(1H)-Quinoxalinethione, 4-oxide is often used as a building block or reagent in the synthesis of other organic compounds, including pharmaceuticals and agrochemicals.
Yellow crystalline solid
2(1H)-Quinoxalinethione, 4-oxide has a yellow color and a crystalline structure.
Molecular weight
The molecular weight of 2(1H)-Quinoxalinethione, 4-oxide is 178.21 g/mol, which is the mass of one mole of the compound.
Biological activities
2(1H)-Quinoxalinethione, 4-oxide has been found to have various biological activities, such as anti-inflammatory, analgesic, and anticonvulsant properties.
Potential use in treating neurodegenerative diseases and cancer
Research has been conducted on the potential use of 2(1H)-Quinoxalinethione, 4-oxide in the treatment of these conditions.
Toxic and harmful if ingested or inhaled
It is important to handle 2(1H)-Quinoxalinethione, 4-oxide with caution as it can be toxic and harmful if ingested or inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 89939-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,3 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89939-20:
(7*8)+(6*9)+(5*9)+(4*3)+(3*9)+(2*2)+(1*0)=198
198 % 10 = 8
So 89939-20-8 is a valid CAS Registry Number.
89939-20-8Relevant academic research and scientific papers
DERIVATIVES OF 3,4-DIHYDRO-3-THIOXO-2-QUINOXALINYLACETIC ACID
Toman, Jaromir,Klicnar, Jiri
, p. 419 - 428 (2007/10/02)
Ethyl 3,4-dihydro-4-methyl-3-thioxo-2-quinoxalinylacetate has been prepared by thionation of the 3-oxo derivative.The mechanism is discussed of the reaction of this ester with diethylamine giving the two non-isomerizing ketimine-enamine tautomers and 1,2-
