96334-44-0

Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 2-AMINO-7-OXO-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBOXYLATE is used as a potential therapeutic agent for various conditions due to the pharmacological properties of benzothiophene compounds, which include anti-inflammatory, antiviral, and anticancer activities.
Further research and studies are essential to fully explore and understand the benefits and applications of ETHYL 2-AMINO-7-OXO-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBOXYLATE, enabling its effective utilization in the development of new drugs and treatments.

Upstream product

• 504-02-9 1,3-cylohexanedione 
• 105-56-6 ethyl 2-cyanoacetate 
• 4506-71-2 ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 
• 52580-57-1 2-benzamide-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid ethyl ester 
• 60442-41-3 2-chloroacetylamino-3-carbethoxy-4,5,6,7-tetrahydrobenzothiophene 
• 62821-69-6 3-Carbethoxy-2-formamido-tetrahydrobenzothiophen 
• 5919-29-9 ethyl 2-acetylamino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 
• 96334-41-7 2-Formylamino-7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester 
• 96334-43-9 2-Benzoylamino-3-ethoxycarbonyl-7-oxo-4,5,6,7-tetrahydrobenzothiophene 
• 96334-42-8 2-(2-Chloro-acetylamino)-7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester 
• 91421-24-8 2-Acetylamino-3-ethoxycarbonyl-7-oxo-4,5,6,7-tetrahydrobenzothiophene 

Downstream Products

• 1202459-14-0 ethyl 2-benzalamino-7-oxocyclohexeno[b]thiophene-3-carboxylate 
• 864961-13-7 7-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluoro-2-nitro-phenyl)-ethyl]-methyl-amide 
• 864961-14-8 7-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluoro-3-nitro-Phenyl)-ethyl]-methyl-amide 
• 893644-78-5 2-amino-7-oxo-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid 
• 96334-46-2 7-oxo-4,5,6,7-tetrahydrobenzothiophene-3-carboxylic acid 

Relevant academic research and scientific papers

Discovery of new thiophene, pyrazole, isoxazole derivatives as antitumor, c-Met, tyrosine kinase and Pim-1 kinase inhibitors

The reaction of cyclohexan-1,3-dione (1) with ethyl orthoformate (2) in acetic acid gave the 2-(ethoxymethylene)cyclohexane-1,3-dione (3). The latter compound was used for further heterocyclization reactions to give thiophene, pyrazole and pyran derivativ

The reaction of cyclohexan-1,3-dione with cyanomethylenes: Synthesis of thiophenes and their fused derivatives with antifungal activities

2-Amino-7-oxotetrahydrobenzo[b]thiophenes 3a,b were prepared according to the Gewald procedure. Their reactivity toward a variety of chemical reagents was studied to give annulated heterocycles with potential bio-responses.

Heterocyclic compound having oxime group

The present invention provides a compound that has an excellent inhibitory activity on STAT6 activation and is effective against allergic diseases, and a medicinal composition thereof. According to the present invention, disclosed is the compound represented by the General Formula (I) [where R1 and R2 independently represent a C1-6 alkyl group and the like that may have a hydrogen atom or a substituent; R3 represents a C1-6 alkyl group and the like that may have a substituent; R4 and R5 independent represents a hydrogen atom or a C1-6 alkyl group and the like that may have a substituent; R6 represents a hydrogen atom and the like; W represents —SO2— and the like; and X represents a sulphur atom and the like.]or a salt thereof, or a hydrate thereof.

SYNTHESIS AND STRUCTURE OF DERIVATIVES OF 7-OXO-4,5,6,7-TETRAHYDROBENZOTHIOPHENE AND 7-HYDROXYBENZOTHIOPHENE

The oxidation of 2-acylamino-3-ethoxycarbonyl-4,5,6,7-tetrahydrobenzothiophenes gave the corresponding 7-oxotetrahydrobenzothiophenes and some of the transformations of these compounds were studied.These compounds were used for the synthesis of 3-et