58585-12-9 Usage
Description
(3-hydroxybenzo[b]thiophen-2-yl)(4-nitrophenyl)methanone is a complex organic compound characterized by a benzo[b]thiophene ring with a hydroxyl group at the 3-position and a 4-nitrophenyl group attached to a ketone carbon. This yellow to brown solid is of interest in pharmaceutical and chemical research due to its unique structure and the presence of a nitro group, which may confer nitroaromatic properties to the compound.
Used in Pharmaceutical Research:
(3-hydroxybenzo[b]thiophen-2-yl)(4-nitrophenyl)methanone is used as a chemical intermediate for the development of new drugs. Its structure and properties make it a promising candidate for the synthesis of complex organic molecules with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, (3-hydroxybenzo[b]thiophen-2-yl)(4-nitrophenyl)methanone serves as a valuable compound for studying the reactivity and properties of nitroaromatic compounds. Its unique structure allows researchers to explore various chemical reactions and transformations, contributing to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 58585-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,8 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58585-12:
(7*5)+(6*8)+(5*5)+(4*8)+(3*5)+(2*1)+(1*2)=159
159 % 10 = 9
So 58585-12-9 is a valid CAS Registry Number.
58585-12-9Relevant articles and documents
Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity
Guglielmi, Paolo,Secci, Daniela,Petzer, Anél,Bagetta, Donatella,Chimenti, Paola,Rotondi, Giulia,Ferrante, Claudio,Recinella, Lucia,Leone, Sheila,Alcaro, Stefano,Zengin, Gokhan,Petzer, Jacobus P.,Ortuso, Francesco,Carradori, Simone
, p. 1511 - 1525 (2019/08/26)
A series of benzo[b]thiophen-3-ols were synthesised and investigated as potential human monoamine oxidase (hMAO) inhibitors in vitro as well as ex vivo in rat cortex synaptosomes by means of evaluation of 3,4-dihydroxyphenylacetic acid/dopamine (DOPAC/DA)
Facile synthesis of 2-substituted benzo[b]thiophen-3-ols in water
Pan, Ben,Ren, Peng,Song, Haibin,Wang, Zhihong
supporting information, p. 1337 - 1344 (2013/05/09)
A facile synthesis of 2-substituted benzo[b]thiophen-3-ols in a simple reaction system is reported with water as the only media. Density functional theory (DFT) investigations suggest two pathways comparable in energetics: A neutral pathway with concerted
Activities of 2-carboxanilido 3-hydroxybenzo[b]thiophens against molluscs Biomphalaria
Gayral,Buisson,Royer
, p. 187 - 189 (2007/10/02)
The title compounds are shown to be nearly as active against molluscs as Niclosamide when they are either dihalogenated or monohalogenated and mononitrated on the benzene ring.
