39256-18-3

Usage

Chemical class

hydrazide derivative

Physical form

white crystalline solid

Stability

stable under normal conditions

Primary use

building block for the synthesis of biologically active compounds

Potential applications

development of new drugs and pesticides

Other uses

production of other hydrazide derivatives, reagent for the determination of various metals in analytical chemistry.

Upstream product

• 6065-82-3 Ethyl diethoxyacetate 

Downstream Products

• 177028-40-9 5-Diethoxymethyl-4-phenyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 177028-43-2 5-Diethoxymethyl-4-(4-nitro-phenyl)-2,4-dihydro-[1,2,4]triazole-3-thione 
• 177028-42-1 4-(4-Bromo-phenyl)-5-diethoxymethyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 177028-41-0 C₁₄H₁₉N₃O₂S 
• 177028-55-6 3-Diethoxymethyl-4-(4-nitro-phenyl)-4H-[1,2,4]triazole 
• 177028-51-2 4-Benzyl-3-diethoxymethyl-4H-[1,2,4]triazole 
• 177028-54-5 4-(4-Bromo-phenyl)-3-diethoxymethyl-4H-[1,2,4]triazole 
• 177028-53-4 3-Diethoxymethyl-4-p-tolyl-4H-[1,2,4]triazole 
• 177028-50-1 4-Cyclohexyl-3-diethoxymethyl-4H-[1,2,4]triazole 
• 177028-52-3 3-Diethoxymethyl-4-phenyl-4H-[1,2,4]triazole 
• 177028-38-5 4-Cyclohexyl-5-diethoxymethyl-2,4-dihydro-[1,2,4]triazole-3-thione 

Relevant academic research and scientific papers

Ion Channel Modulators

The invention relates to compounds, compositions comprising the compounds, and methods of using the compounds and compound compositions. The compounds, compositions, and methods described herein can be used for the therapeutic modulation of ion channel function, and treatment of disease and disease symptoms, particularly those mediated by certain calcium channel subtype targets.

ION CHANNEL MODULATORS

The invention relates to compounds, compositions comprising the compounds, and methods of using the compounds and compound compositions. The compounds, compositions, and methods described herein cab be used for the therapeutic modulation of ion channel fu

Precursors for the synthesis of substituted 1,3,4-thiadiazole C- nucleosides, analogues of tiazofurin and related compounds

The synthesis of 2-substituted 1,3,4-thiadiazole C-glycosides is described by building a heterocyclic system at the aldehyde end of a series of sugar derivatives. Acid catalyzed dehydration of the polyhydroxylic chain resulted in C-nucleoside, an analogue of tiazofurin.