1457-39-2

Upstream product

• 5469-36-3 n-butylfumaric acid 
• 61040-89-9 4-methyl-3,5-dioxo-cyclohexanecarboxylic acid 
• 67610-46-2 ethyl 3,3-dicarbethoxyheptanoate 
• 25236-79-7 2-n-Butyl-4,4,4-trichlor-ethylbutyrat 
• 996-82-7 sodium diethylmalonate 
• 105-39-5 chloroacetic acid ethyl ester 
• 25236-78-6 2-n-Butyl-4,4,4-trichlorbutyramid 
• 42858-60-6 3,5-cyclohexanedione-1-carboxylic acid 
• 133-08-4 diethyl butylmalonate 
• 308349-48-6 3-(tert-butoxycarbonyl)heptanoic acid 
• 79-08-3 bromoacetic acid 
• 142-62-1 hexanoic acid 
• 135386-87-7 5-hydroxy-4-butyl-4,5-dihydro-3H-furan-2-one 
• 110-62-3 pentanal 

Downstream Products

• 2035-76-9 3-butyldihydrofuran-2,5-dione 
• 4136-86-1 dimethyl 2-butylsuccinate 
• 101434-34-8 2-Butyl-bernsteinsaeure-dibutylester 
• 34722-01-5 3-butylthiophene 

Relevant academic research and scientific papers

Synthesis of monosubstituted succinic acids from tert-butylsuccinate

We report the preparation and alkylation of the dianion of t-butylsuccinate. This alkylation reaction has proven to be a useful method for the preparation of monosubstituted succinic acids and anhydrides.

STERICALLY SCREENED HALOGENOCYCLOBUTANONES VI. SYNTHESIS OF 3-FORMYLPROPIONIC ACIDS FROM DICHLOROCYCLOBUTANONES

3-Formylpropionic acids can be obtained with good yields by the treatment of 2,2-dichlorocyclobutanones with an aqueous solution of potassium hydroxide.

Inhibition of Liver Alcohol Dehydrogenase and Ethanol Metabolism by 3-Substituted Thiolane 1-Oxides

3-Substituted thiolane oxides (methyl, n-butyl, n-hexyl, and phenyl) were prepared and tested as inhibitors of horse, monkey, and rat liver alcohol dehydrogenases and of ethanol metabolism in rats.These compounds inhibit alcohol oxidation in an uncompetit

Polymers of sulfonic acid monomers

The present invention is concerned with novel monomers containing sulfonic acid groups or salts thereof and polymers thereof which are useful for many purposes, such as antistatic agents for textiles and other shaped articles formed of hydrophilic materials. They are useful for making copolymers that are particularly valuable in coating compositions, especially in the form of aqueous latices or organic solvent solutions thereof. Examples of the monomers are of the formula STR1 wherein R is hydrogen or lower (C1 -C4)alkyl, such as methyl, A is an alkylene group having 2 to 10 carbon atoms, at least 2 of which extend in one chain between the oxygen atoms, and X is an aromatic nucleus or an alkyl group, substituted by a sulfonic acid group and optionally one or more groups selected from sulfonic acid, carboxylic acid, and lower alkyl, such as methyl, ethyl, propyl, or butyl.