4170-84-7

Usage

Uses

Used in Chemical Industry:
(1,1-DIETHYLPROPYL)BENZENE is used as a solvent for its ability to dissolve a wide range of substances, facilitating various chemical processes and reactions.
Used in Dye Manufacturing:
(1,1-DIETHYLPROPYL)BENZENE is used as a component in the production of dyes, contributing to the coloration and stability of the final products.
Used in Pharmaceutical Production:
(1,1-DIETHYLPROPYL)BENZENE is used in the manufacturing of pharmaceuticals, playing a role in the synthesis of various medicinal compounds.
Used in Flavor and Fragrance Industry:
(1,1-DIETHYLPROPYL)BENZENE is used as a flavor and fragrance ingredient in perfumes and cosmetics, enhancing the sensory experience of these products.

InChI:InChI=1/C13H20/c1-4-13(5-2,6-3)12-10-8-7-9-11-12/h7-11H,4-6H2,1-3H3

Upstream product

• 74-85-1 ethene 
• 103-65-1 phenylpropane 
• 597-49-9 3-ethylpentan-3-ol 
• 71-43-2 benzene 
• 73908-04-0 triethylcarbinyl bromide 
• 23418-91-9 9-phenyl-9-borabicyclo[3.3.1]nonane 
• 98-08-8 α,α,α-trifluorotoluene 
• 97-93-8 triethylaluminum 
• 7446-70-0 aluminium trichloride 
• 35354-15-5 2,2-diethylbutanoyl chloride 
• 35078-49-0 (1-ethyl-1-chloropropyl)benzene 
• 2386-64-3 ethylmagnesium chloride 
• 994-25-2 3-ethyl-3-chloro-pentane 

Downstream Products

• 37872-27-8 4-(1,1-diethyl-propyl)-benzoic acid 
• 67467-91-8 3-[p-(1,1-diethyl-propyl)-phenyl]-2-methyl-propionaldehyde 
• 37872-23-4 4-(triethylmethyl)aniline 
• 37872-21-2 1-(4-bromophenyl)-1,1,1-triethylmethane 
• 37872-22-3 1-(1,1-diethyl-propyl)-4-nitro-benzene 

Relevant academic research and scientific papers

Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations

The first Suzuki cross-couplings of unactivated tertiary alkyl electrophiles are described. The method employs a readily accessible catalyst (NiBr2·diglyme/4,4′-di-tert-butyl-2,2′-bipyridine, both commercially available) and represents the initial example of the use of a group 10 catalyst to cross-couple unactivated tertiary electrophiles to form C-C bonds. This approach to the synthesis of all-carbon quaternary carbon centers does not suffer from isomerization of the alkyl group, in contrast with the umpolung strategy for this bond construction (cross-coupling of a tertiary alkylmetal with an aryl electrophile). Preliminary mechanistic studies are consistent with the generation of a radical intermediate along the reaction pathway.

Carbon-carbon coupling of C(sp3)-F bonds using alumenium catalysis

Dialkylalumenium cation equivalents coupled with the hexabromocarborane anion function as efficient and long-lived catalysts for alkylation of aliphatic C-F bonds (alkylative defluorination or AlkDF) by alkylaluminum compounds. Only C(sp3)-F bo