1681-17-0

Usage

Uses

Used in Pharmaceutical Industry:
3-Acetyl-3-methylpentanedicarbonitrile is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its high reactivity allows it to be a key component in the production of drugs that target a range of medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Acetyl-3-methylpentanedicarbonitrile is employed as an intermediate in the development of agrochemicals. Its role in this industry is crucial for creating compounds that contribute to crop protection and enhancement of agricultural yields.
Used in Chemical Synthesis:
3-Acetyl-3-methylpentanedicarbonitrile is used as a building block in the synthesis of other chemical compounds. Its structural properties make it a valuable precursor for creating a variety of organic compounds used in different industries, including but not limited to, the production of specialty chemicals and materials.

InChI:InChI=1/C10H14N2O/c1-9(13)10(2,5-3-7-11)6-4-8-12/h3-6H2,1-2H3

Upstream product

• 107-13-1 acrylonitrile 
• 78-93-3 butanone 
• 109-78-4 3-Hydroxypropionitrile 
• 3744-02-3 4-methylpent-4-en-2-one 
• 542-76-7 3-Chloropropionitrile 

Downstream Products

• 19830-09-2 4-acetyl-4-methyl-heptanedioic acid 
• 2035-91-8 4-Methyl-4-acetyl-pimelinsaeure-diethylester 
• 20141-99-5 3-(4-Amino-1-methyl-2-oxo-cyclohex-3-enyl)-propionitrile 
• 90872-93-8 4-Imino-1-methyl-1-(2-cyan-ethyl)-cyclohexanon-⁽²⁾ 
• 6848-93-7 4-acetyl-4-methyl cyclohexanone 
• 10531-03-0 1-methyl-4-morpholinocyclohex-3-enyl methyl ketone 
• 3907-11-7 4-Methoxy-1-methyl-bicyclo<2.2.2>octan-2-on 
• 702-67-0 4-methylbicyclo<2.2.2>octane-1-carboxylic acid 
• 824-13-5 4-Methylbicyclo<2.2.2>octan-1-ol 
• 7697-06-5 1-Chlor-4-methyl-bicyclo<2.2.2>octan 
• 55044-63-8 1-iodo-4-methylbicyclo<2.2.2>octane 
• 697-40-5 1-bromo-4-methylbicyclo<2.2.2>octane 
• 54644-25-6 4-Acetoxy-1-methyl-bicyclo<2.2.2>octan 
• 5122-77-0 4-hydroxy-1-methylbicyclo[2.2.2]octan-2-one 

Relevant academic research and scientific papers

Transmission of Polar Substituent Effects Through the Bicyclooctane Ring System as Monitored by NMR Shifts: a 13C NMR Study of 4-Substituted-1-methylbicyclooctanes

Carbon-13 substituent chemical shifts (SCS) are reported for the methyl group of a series of 4-substituted 1-methylbicyclooctanes covering a wide range of electronic substituent effects.Unlike the 13C SCS of the α-carbon centre in various unsaturat

4-acetyl-4-methylheptanedinitrile at 173 K

The title compound, C10H14N2O, serves as an precursor for ring-closure reactions to afford, for example, naphthyridines and quinolinediones. In the crystal, the molecule does not show any pre-organization favouring a ring closure; the heptanedinitrile chain is almost antiperi-planar, with the C-C-C angles having nearly perfect tetrahedral values.

The Synthesis of 1,4-Disubstituted Bicyclooctanes exhibiting Wide-range, Enantiotropic Nematic Phases

The 1,4-disubstituted bicyclooctane ring has been incorporated in certain cyano-substituted systems to produce series of mesogens exhibiting wide-range nematic phases. 1-(4-Cyanophenyl)- and 1-(4'-cyanobiphenyl-4-yl)-4-n-alkylbicyclooctanes