4170-84-7 Usage
Description
(1,1-DIETHYLPROPYL)BENZENE, also known as di-n-propyltoluene, is a chemical compound characterized by the molecular formula C12H18. It is a colorless liquid with a strong aromatic odor, and it is recognized for its versatility in various industrial applications.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 4170-84-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,7 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4170-84:
(6*4)+(5*1)+(4*7)+(3*0)+(2*8)+(1*4)=77
77 % 10 = 7
So 4170-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H20/c1-4-13(5-2,6-3)12-10-8-7-9-11-12/h7-11H,4-6H2,1-3H3
4170-84-7Relevant articles and documents
Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations
Zultanski, Susan L.,Fu, Gregory C.
supporting information, p. 624 - 627 (2013/03/14)
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.
