CAS 58980-39-5

2,3,4,5-Tetrahydrobenzo[F][1,4]Thiazepine

Description:

2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine is a bicyclic compound that features a thiazepine ring, which is a seven-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound is characterized by its fused benzene and thiazepine rings, contributing to its unique chemical properties. It typically exhibits a moderate level of lipophilicity due to the presence of aromatic and aliphatic components, which can influence its solubility in organic solvents. The thiazepine moiety may impart biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound's structure allows for potential interactions with various biological targets, and it may exhibit properties such as analgesic or anxiolytic effects, although specific biological activities can vary. Additionally, its stability and reactivity can be influenced by the substituents on the ring system, which can affect its synthesis and application in various chemical contexts. Overall, 2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine represents a versatile scaffold in organic and medicinal chemistry.

2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine

CAS: 58980-39-5

Formula: C₉H₁₁NS

Molecular weight: 165.2553

Ref: IN-DA00EJAS

2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine

CAS: 58980-39-5

Formula: C₉H₁₁NS

Purity: 95.0%

Color and Shape: Liquid

Molecular weight: 165.25

Ref: 10-F226027

2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine

CAS: 58980-39-5

2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine is a benzothiazepine that has neuroprotective properties. It is synthesized in two steps from 2-nitrobenzaldehyde and 4-aminophenylacetic acid. 2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine is used as a neuroprotective agent to treat neurological disorders such as Parkinson's disease and cerebral infarction. The drug can be hydrolyzed to tetrahydrobenzo[f][1,4]thiazepin-2(3H)-one by alkaline phosphatase and the carboxylic acid moiety can be converted to an ester by reacting with an alcohol. The nitro group can be reduced to an amino group by sodium borohydride or hydrogenation with palladium on charcoal.

Formula: C₉H₁₁NS

Purity: Min. 95%

Molecular weight: 165.25 g/mol

Ref: 3D-ICA98039