28544-77-6 Usage
General Description
Pyridazine-3-thiol is a chemical compound with the molecular formula C4H4N2S. It is a heterocyclic organic compound with a sulfur atom and a nitrogen atom in the six-membered ring. Pyridazine-3-thiol is a yellow crystalline solid and is commonly used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. It is also known for its potential biological activities, including antibacterial, antifungal, and antitumor properties. Additionally, it has been studied for its potential applications in materials science, such as in the development of corrosion inhibitors and electroactive materials. Overall, pyridazine-3-thiol is a versatile and important chemical compound with diverse applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 28544-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,4 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28544-77:
(7*2)+(6*8)+(5*5)+(4*4)+(3*4)+(2*7)+(1*7)=136
136 % 10 = 6
So 28544-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N2S/c7-4-2-1-3-5-6-4/h1-3H,(H,6,7)
28544-77-6Relevant articles and documents
PARP INHIBITORS
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Page/Page column 34; 35, (2013/03/28)
The present application disclosed compounds of Formula I wherein variables R1 and R2 are defined as described herein, which are inhibitors of PARP and provides compounds and compositions containing the compounds of Formula I. The pre
6-SUBSTITUTED- 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS
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Page/Page column 64, (2008/06/13)
The present invention provides 6-substituted 2,3,4,5-tetrahydro-lH- benzo[d]azepines of Formula (I) as selective 5-HT2C receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety: R6 D R? N-R" R* where R6 is -(CrC3)alkyl-S-(C0-C3)alkyl-R10, -(C1-C3)alkyl-NR11R12, -(CrC3)alkyl-O- R 13. and other substituents are as defined in the specification.
Cephalosporin displacement reaction
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, (2008/06/13)
The present invention is directed to a process for the displacement of the acetoxy group of a cephalosporanic acid by a sulfur nucleophile, in an organic solvent and under essentially anhydrous conditions.
