274-26-0 Usage
Heterocyclic compound
1,3-Benzoxathiole is a compound that contains a ring of atoms with at least one heteroatom, which is an atom other than carbon.
Benzene ring fused to a thiophene ring
The chemical structure of 1,3-Benzoxathiole consists of a benzene ring fused to a thiophene ring, which is a five-membered ring containing sulfur.
Oxygen atom
The chemical structure of 1,3-Benzoxathiole also includes an oxygen atom.
Potent biological activities
1,3-Benzoxathiole has been found to have potent biological activities, including antitumor, anti-inflammatory, and antimicrobial properties.
Pharmacophore
The chemical structure of 1,3-Benzoxathiole makes it an important pharmacophore, which is a part of a molecule that is responsible for its biological activity.
Medicinal chemistry
1,3-Benzoxathiole is an important compound in the field of medicinal chemistry, which is the study of how drugs work and how they can be used to treat diseases.
Development of new drugs
The unique structure and diverse pharmacological activities of 1,3-Benzoxathiole make it a promising candidate for the development of new drugs.
Treatment of cancer, inflammation, and infectious diseases
1,3-Benzoxathiole has potential therapeutic benefits in the treatment of cancer, inflammation, and infectious diseases.
Further research and studies needed
Further research and studies are needed to fully understand the potential of 1,3-Benzoxathiole in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 274-26-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 274-26:
(5*2)+(4*7)+(3*4)+(2*2)+(1*6)=60
60 % 10 = 0
So 274-26-0 is a valid CAS Registry Number.
274-26-0Relevant articles and documents
Bimolecular coupling reactions through oxidatively generated aromatic cations: Scope and stereocontrol
Cui, Yubo,Villafane, Louis A.,Clausen, Dane J.,Floreancig, Paul E.
, p. 7618 - 7626 (2013/08/23)
Chromenes, isochromenes, and benzoxathioles react with 2,3-dichloro-5,6- dicyano-1,4-benzoquinone to form stable aromatic cations that react with a range of nucleophiles. These oxidative fragment coupling reactions provide rapid access to structurally div
A re-examination of the methylenation reaction
Cabiddu, Maria Grazia,Cadoni, Enzo,De Montis, Stefania,Fattuoni, Claudia,Melis, Stefana,Usai, Michele
, p. 4383 - 4387 (2007/10/03)
A re-examination of the methylenation reaction of 1-hydroxy-2-mercapto-, 1,2-dihydroxy- and 1,2-dimercapto-substituted benzenes by bromochloromethane with cesium carbonate shows that these substrates give mixtures of five- and ten-membered benzocondensed heterocyclic compounds and in some cases even dibenzodioxines.
