7019-91-2 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-(2-methylpropylidene)is used as a building block for the synthesis of various pharmaceuticals. Its high stability and versatile nature make it an important chemical in the production of medicines.
Used in Agrochemical Industry:
2,5-Cyclohexadien-1-one,
2,6-bis(1,1-dimethylethyl)-4-(2-methylpropylidene)is also used in the agrochemical industry as a precursor for the synthesis of various agrochemicals. Its stability and reactivity contribute to the development of effective agricultural products.
Used in Fragrance and Flavor Industry:
2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-(2-methylpropylidene)is used as a precursor in the manufacturing of fragrances and flavors. Its ability to be incorporated into complex organic compounds makes it valuable in creating high-quality and long-lasting scents and tastes.
Used in Fine Chemicals Industry:
In the fine chemicals industry, 2,5-Cyclohexadien-1-one,
2,6-bis(1,1-dimethylethyl)-4-(2-methylpropylidene)- is utilized for the synthesis of various high-value products. Its versatility and stability make it an essential component in the production of specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 7019-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7019-91:
(6*7)+(5*0)+(4*1)+(3*9)+(2*9)+(1*1)=92
92 % 10 = 2
So 7019-91-2 is a valid CAS Registry Number.
7019-91-2Relevant academic research and scientific papers
Ghosh, Krishna Gopal,Chandu, Palasetty,Mondal, Santanu,Sureshkumar, Devarajulu
, p. 4471 - 4478 (2019)
A transition metal free visible light mediated organo photoredox catalyzed trifluoromethylation of p-quinone methides (p-QMs) to construct fluoro-analogs of dichlorodiphenyltrichloroethane (DDT) is reported using a bench stable, inexpensive Langlois reagent as a trifluoromethyl radical source. This protocol could generate a benzylic C(sp3)-CF3 bond with excellent yield under mild reaction conditions using 1,6-conjugate addition/aromatization of trifluoromethyl radical in the absence of any external additives. Further, we demonstrate di-trifluoromethylation and gram scale synthesis of this reaction.
Process for the preparation of 2,6-di-tert.-alkyl-4-alkylidene-2,5-cyclohexadien-ones
-
, (2008/06/13)
A process for preparing a 2,6-di-tert-alkyl-4-alkylidene-2,5-cyclohexadien-one which comprises contacting a bis-(3,5-di-tert.-alkyl-4-hydroxybenzyl)sulphide of the formula STR1 wherein R1 denotes a tertiary alkyl group and R2 denotes hydrogen, a straight or branched alkyl, cycloalkyl, cycloalkenyl, aralkyl or aryl group with lead or mercury in the oxide, hydroxide, carbonate, acetate or other basic reacting salt form at an elevated temperature in an inert solvent.
