19282-45-2

Usage

Uses

Used in Pharmaceutical Industry:
TIMTEC-BB SBB005657 is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drug compounds.
Used in Dye Industry:
TIMTEC-BB SBB005657 is used as an intermediate in the production of dyes, where its chemical properties are utilized to create a variety of colorants for different applications.
Used in Organic Synthesis:
TIMTEC-BB SBB005657 is used as a building block in the synthesis of various organic compounds, playing a crucial role in the creation of complex molecules for a range of applications.

InChI:InChI=1/C11H14O2S/c1-2-13-11(12)10-7-8-5-3-4-6-9(8)14-10/h7H,2-6H2,1H3

Upstream product

• 38127-47-8 2-bromocyclohex-1-ene-1-carbaldehyde 
• 623-51-8 ethyl 2-sulfanylacetate 
• 49571-45-1 2-(methylthio)cyclohex-1-ene-1-carbaldehyde 
• 1680-73-5 2-chlorocyclohexene-1-carboxaldehyde 

Downstream Products

• 65361-27-5 4,5,6,7-tetrahydro-1-benzothiophene-2-carbohydrazide 
• 65361-26-4 4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxylic acid chloride 

Relevant academic research and scientific papers

Base catalyzed reaction of ethyl thioglycolate with β-aryl-β-(methylthio) acroleins: A general method for the synthesis of 2-carbethoxy-5-substituted/4,5-annulated thiophenes in high overall yields

(Methylthio) acroleins 1a-m were shown to be stable unlike their counterpart the chloroacroleins and their efficacy as 1,3-dielectrophilic properties have now been examined successfully in this work. They are shown to react with ethyl thioglycolate in the

KF/Al2O3/PEG-400: An efficient catalytic system for the fiesselmann-type synthesis of thiophene derivatives

A simple and mild protocol has been developed for the synthesis of novel steroidal and nonsteroidal thiophene derivatives from β-halo-α, β-unsaturated aldehydes using KF/Al2O3/PEG-400 as an efficient catalytic system. The β-halo-α,β-

Synthesis, cytotoxicity and effects of some 1,2,4-triazole and 1,3,4-thiadiazole derivatives on immunocompetent cells

Novel derivatives of 4,5-substituted-1,2,4-triazole-thiones and 2,5-substituted-1,3,4-thiadiazoles were synthesized and evaluated for their cytotoxicity. The biological study indicated that compounds 4-ethyl-5-(4,5,6,7-tetrahydro-1-benzothien-2-yl)-2,4-di