30484-10-7

Usage

Explanation

This is the formal IUPAC name for the compound, which describes its structure and functional groups.

Explanation

The compound has a fused ring system consisting of a benzene ring, a thiophene ring, and a dihydro-1H-1-benzazepin-2-one core. The chlorine atom is attached at the 7th position of the benzothiepin ring.

Explanation

The chemical formula represents the elements and their quantities in the compound. In this case, it consists of 12 carbon atoms, 10 hydrogen atoms, 1 chlorine atom, 1 nitrogen atom, and 1 sulfur atom.

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule.

Explanation

Due to its structural and pharmacological properties, 1-Benzothiepin-5(2H)-one, 7-chloro-3,4-dihydro- may be used in pharmaceutical research and has the potential to be developed into a drug candidate.

Explanation

The compound's specific biological activities are not detailed in the provided material, but its potential for further study and development in the scientific community suggests that it may have relevant biological properties.

Explanation

The compound's complex molecular structure and potential pharmacological properties make it a valuable subject for research in the field of drug development and medicinal chemistry.

Explanation

The solubility of the compound in various solvents is not mentioned in the provided material, which is an important property for understanding its behavior in different environments.

Explanation

The stability of the compound under different conditions (e.g., temperature, pH, light exposure) is not mentioned in the provided material, which is crucial for its handling, storage, and potential applications.

Explanation

The safety and toxicity profiles of the compound are not detailed in the provided material, which are essential factors to consider when working with chemicals, especially in a pharmaceutical context.

Molecular Structure

Benzothiepin ring with a chlorine atom at the 7th position and a 3,4-dihydro-1H-1-benzazepin-2-one core.

Molecular Weight

Approximately 247.7 g/mol

Pharmacological Properties

Potential applications as a drug candidate.

Biological Activities

May have biological activities of interest for further study and development.

Research Applications

Used in pharmaceutical research.

Solubility

Information on solubility is not provided in the material.

Stability

Information on stability is not provided in the material.

Safety and Toxicity

Information on safety and toxicity is not provided in the material.

Upstream product

• 29193-63-3 4-(4-chlorophenylthio)butyric acid 
• 106-54-7 p-Chlorothiophenol 

Downstream Products

• 76867-51-1 9-Chloro-10b-morpholin-4-yl-1-(4-nitro-phenyl)-3a,4,5,10b-tetrahydro-1H-6-thia-1,2,3-triaza-benzo[e]azulene 
• 76867-50-0 9-Chloro-1-(4-nitro-phenyl)-10b-pyrrolidin-1-yl-3a,4,5,10b-tetrahydro-1H-6-thia-1,2,3-triaza-benzo[e]azulene 
• 76867-46-4 [9-Chloro-1-(4-nitro-phenyl)-1,3a,4,5-tetrahydro-6-thia-1,2,3-triaza-benzo[e]azulen-10b-yl]-dimethyl-amine 
• 76867-49-7 9-Chloro-1-(4-chloro-phenyl)-10b-pyrrolidin-1-yl-3a,4,5,10b-tetrahydro-1H-6-thia-1,2,3-triaza-benzo[e]azulene 
• 76867-44-2 [9-Chloro-1-(4-fluoro-phenyl)-1,3a,4,5-tetrahydro-6-thia-1,2,3-triaza-benzo[e]azulen-10b-yl]-dimethyl-amine 
• 118258-12-1 10-Chloro-2-(4'-methoxyphenyl)-4,4a,5,6-tetrahydro-(1)benzothiepino<5,4-c>pyridazin-3(2H)-one 
• 118258-13-2 10-Chloro-2-(4'-chlorophenyl)-4,4a,5,6-tetrahydro-(1)benzothiepino<5,4-c>pyridazin-3(2H)-one 
• 118271-62-8 10-Chloro-2-(4'-chlorophenyl)-5,6-dihydro-(1)benzothiepino<5,4-c>pyridazin-3(2H)-one 
• 118288-66-7 10-chloro-2-(4-chlorophenyl)-5,6-dihydro-⁽¹⁾benzothiepino[5,4-c]pyridazine-3(2H)-one 7-oxide 

Relevant academic research and scientific papers

Thiochroman-4-one thiosemicarbazide compound as well as preparation method and application thereof

The invention relates to a thiochroman-4-one thiosemicarbazide compound, as well as a preparation method and an application thereof. The structural formula of the thiochroman-4-one thiosemicarbazide compound is shown as Formula (I), wherein n is 1 or 2, R