4436-99-1

Usage

Uses

Used in Pharmaceutical Industry:
Dineopentylketone is used as a solvent in the synthesis of pharmaceuticals for its ability to dissolve a wide range of compounds, facilitating the production of various medications.
Used in Perfumery and Flavoring Industry:
It serves as a solvent in the creation of perfumes and flavorings, enhancing the extraction and stability of aromatic compounds due to its sweet, floral scent.
Used in Chemical Production:
Dineopentylketone is utilized in the production of other important chemicals, including those used in agriculture and the manufacturing of plastics, contributing to the development of a diverse range of products.
Used in Cosmetic and Personal Care Products:
Given its low toxicity and non-irritating properties to the skin, dineopentylketone is a preferred solvent in the formulation of cosmetic and personal care products, ensuring both safety and effectiveness.

InChI:InChI=1/C11H22O/c1-10(2,3)7-9(12)8-11(4,5)6/h7-8H2,1-6H3

Upstream product

• 141-70-8 1,1-dineopentylethylene 
• 201230-82-2 carbon monoxide 
• 61382-45-4 (E)-1-iodo-3,3-dimethyl-1-butene 
• 123-48-8 pentamethyl-2,2,4,6,6 heptene-3 

Downstream Products

• 20818-95-5 trineopentylcarbinol 
• 40543-97-3 4-Nitro-benzoic acid 1-(4-chloro-phenyl)-1-(2,2-dimethyl-propyl)-3,3-dimethyl-butyl ester 
• 40543-96-2 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester 
• 40543-95-1 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-p-tolyl-butyl ester 
• 40543-98-4 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-(4-trifluoromethyl-phenyl)-butyl ester 
• 40544-08-9 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-1,3,3-trimethyl-butyl ester 
• 22822-86-2 2-tert.-Butyl-1-neopentyl-vinyl-p-nitrobenzoat 
• 20818-93-3 4-(2,2-dimethyl-propyl)-2,2,6,6-tetramethyl-4-(4-nitro-benzoyloxy)-heptane 
• 1070-83-3 tert-Butylacetic acid 
• 75-98-9 Trimethylacetic acid 
• 20818-92-2 4-tert-butyl-2,2,6,6-tetramethyl-4-(4-nitro-benzoyloxy)-heptane 
• 40544-17-0 4-Phenyl-2,2,6,6-tetramethylheptan 
• 19985-79-6 2,3-bis(tert-butyl)cycloprop-2-en-1-one 

Relevant academic research and scientific papers

Palladium/Rhodium Cooperative Catalysis for the Production of Aryl Aldehydes and Their Deuterated Analogues Using the Water–Gas Shift Reaction

A novel Pd/Rh dual-metallic cooperative catalytic process has been developed to effect the reductive carbonylation of aryl halides in moderate to good yield. In this reaction, water is the hydride source, and CO serves both as the carbonyl source and the terminal reductant through the water–gas shift reaction. The catalytic generation of the Rh hydride allows for the selective formation of highly hindered aryl aldehydes that are inaccessible through previously reported reductive carbonylation protocols. Moreover, aldehydes with deuterated formyl groups can be efficiently and selectively synthesized using D2O as a cost-effective deuterium source without the need for presynthesizing the aldehyde.

PROCESS FOR PREPARING KETONES BY REACTING 1,1-DISUBSTITUTED OLEFINS WITH N2O

The present invention relates to a process for preparing a ketone, comprising the reaction of a composition (I) at least comprising a 1,1-disubstituted olefin, with a composition comprising dinitrogen monoxide, wherein the reaction is effected in the presence of a solvent which comprises at least one proton-donating functional group.

NEOPENTYL COMPLEXES OF PALLADIUM

New dineopentyl complexes of palladium, with the formula (L2 = dppe, bipy; L = PMe2Ph) have been prepared by the alkylation of the corresponding dichlorides with Mg(CH2CMe3)Br or LiCH2CMe3.Thermal decomposition of these complexes in solution yields 2,2,5,5-tetramethylhexane.The reactions of these compounds with CO and with some electrophiles (Ph3C+, PhCH2Br, HCl) have been investigated.The reaction with CO produces dineopentyl ketone (when L2 = dppe; L = PMe2Ph) or promotes rapid decomposition to 2,2,5,5-tetramethylhexane (when L2 = bipy).The electrophiles (E+) attack the neopentyl ligand to eliminate ECH2CMe3.In the reaction of with PhCH2Br, has been isolated.A palladacyclic analogue of these systems, , has been prepared by the alkylation of with Li(CH2CMe2CMe2CH2)Li.