2,2-Dimethylbut-3-enoic acid, also known as 2,2-dimethyl-3-butenoic acid, is an unsaturated carboxylic acid characterized by its double bond and branched structure. It features a four-carbon backbone with two methyl groups attached to the second carbon and a double bond between the third and fourth carbons. This structure contributes to its reactivity, particularly in addition reactions typical of alkenes. The presence of the carboxylic acid functional group (-COOH) imparts acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. The compound is typically a colorless liquid or solid at room temperature and is soluble in polar solvents due to its polar carboxylic acid group. Its unique structure makes it a valuable intermediate in organic synthesis, particularly in the production of polymers and other chemical derivatives. Safety data should be consulted for handling, as it may pose health risks if ingested or inhaled.

2,2-dimethylbut-3-enoic acid

10276-09-2: 3-Butenoic acid, 2,2-dimethyl-

2,2-Dimethylbut-3-enoic acid

3-Butenoic acid, 2,2-dimethyl-

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2,2-Dimethyl-3-butenoic acid, 95%

2,2-Dimethylbut-3-enoic acid is a bioactive compound that is used to synthesize other compounds. It has been shown to have a number of functions, such as being an electrolyte and having an electron deficient group in its structure. 2,2-Dimethylbut-3-enoic acid reacts with electrophilic functional groups at high temperatures to form allylation products. This reaction is called cheletropic and has been shown to be reversible.

CAS 10276-09-2: 2,2-dimethylbut-3-enoic acid

2,2-Dimethylbut-3-enoic acid

Ref: 54-OR937784

3-Butenoic acid, 2,2-dimethyl-

Ref: IN-DA0008BA

2,2-Dimethyl-3-butenoic acid, 95%

Ref: 02-H64067

2,2-Dimethylbut-3-enoic acid

Ref: 3D-KAA27609

2,2-Dimethylbut-3-enoic acid

Ref: 10-F790829