56658-35-6

Usage

Uses

Used in Pharmaceutical Synthesis:
2-(3,3-dimethyl-2-oxobutyl)-1H-isoindole-1,3(2H)-dione is used as a precursor in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a key component in the development of new drugs.
Used in Organic Chemistry:
In the field of organic chemistry, 2-(3,3-dimethyl-2-oxobutyl)-1H-isoindole-1,3(2H)-dione is used as a building block for creating more complex molecules. Its reactivity and structural properties make it a valuable component in the synthesis of advanced organic compounds.
Used in Drug Development:
Due to its potential applications, 2-(3,3-dimethyl-2-oxobutyl)-1H-isoindole-1,3(2H)-dione is also used in the development of new drugs and materials. Its unique properties may contribute to the creation of innovative pharmaceuticals and other materials with novel applications.

InChI:InChI=1/C14H15NO3/c1-14(2,3)11(16)8-15-12(17)9-6-4-5-7-10(9)13(15)18/h4-7H,8H2,1-3H3

Upstream product

• 1074-82-4 potassium phtalimide 
• 5469-26-1 1-Bromopinacolon 
• 13547-70-1 1-chloro-3,3-dimethyl-butan-2-one 
• 1313233-00-9 C₁₄H₁₃NO₂ 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 136918-14-4 phthalimide 

Downstream Products

• 14395-90-5 4-tert-butyl-1,3-dihyroimidazole-2-thione 
• 859951-94-3 N-(3,3-dimethyl-2-oxo-butyl)-phthalamic acid 
• 33119-72-1 1-amino-3,3-dimethylbutan-2-one hydrochloride 

Relevant academic research and scientific papers

Synthesis of 6aλ4-Thia-1,2,3,5,6-pentaazapentalenes

The title compounds have been obtained from 5-amino-1,2,3-thiadiazole 6 by methylation and reaction with arenediazonium tetrafluoroborates; their 13C NMR data and X-ray analysis are discussed in terms of two non-equivalent resonance contributors 11A and 11B.

Ag-and Au-catalyzed addition of alcohols to ynimides: β-regioselective carbonylation and production of oxazoles

Metal-catalyzed reactions of ynimides with alcohols to afford β-ketoimides and oxazoles are demonstrated. The triple bond of ynamides is generally activated by mineral acids or metal salts to lead to the regioselective addition of nucleophiles at the α-C-

Palladium-catalyzed asymmetric hydrogenation of functionalized ketones

(Chemical Equation Presented) A novel catalytic system for asymmetric hydrogenation of functionalized ketones has been developed using a Pd/bisphosphine complex as the catalyst in 2,2,2-trifluoroethanol. The reaction exhibits high enantioselectivity, and

Concise synthesis of 1H-pyrazin-2-ones and 2-aminopyrazines

Convenient syntheses of 1H-pyrazin-2-ones and 2-aminopyrazines are described. By coupling Boc-protected amino acids with α-amino ketones or with amino alcohols and subsequent oxidation, 1H-pyrazin-2-ones were obtained. Transformation into the corresponding pyrazine triflates and substitution with primary or secondary amines led to 2-aminopyrazines. Since these syntheses take advantage of the use of readily available starting materials (e.g., amino acids, aminoalcohols and amines) a variety of the entitled structures can be obtained in few, high yielding steps.

Oxazole carboxamide herbicides

The novel compounds of formula I: wherein R1, R2, R3, R4 and Ar have the meaning given in claim 1, and herbicidal compositions containing such compounds as active ingredients.

Insecticidal compositions and methods of combatting insects using substituted imidazoles

Insecticidal composition comprising a compound of the formula SPC1 In which X is selected from the group consisting of oxygen and sulphur, R3 is selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, R4 is s

Thio derivatives of imidazol-1-yl carboxamides

Novel imidazole compounds, pesticidal compositions and methods of using them, and their preparation are described. The compounds have the formula STR1 in which X is oxygen or sulphur, R3 is hydrogen, alkyl, alkenyl or optionally substituted alkylthio, alkenylthio, aralkylthio, alkoxyalkyl or alkylthioalkyl, R4 is alkyl or cycloalkyl, and R1 and R2 are each lower alkyl or alkenyl, R1 is lower alkyl and R2 is alkoxyalkyl or haloalkyl, or R1 and R2 together with the nitrogen atom to which they are attached, form an optionally substituted heterocyclic ring; and salts thereof. Novel compounds are of particular value against insects e.g. aphids, and against other pests, e.g. acarids.