54200-67-8 Usage
Uses
Used in Fragrance Industry:
2,3,6-Trimethylacetophenone is used as a fragrance ingredient for its sweet, floral scent in perfumes, soaps, and other personal care products.
Used in Flavoring Industry:
2,3,6-Trimethylacetophenone is used as a flavoring agent in food products to impart a unique taste and aroma.
Used in Pharmaceutical Production:
2,3,6-Trimethylacetophenone is used in the production of pharmaceuticals, contributing to the development of various medications.
Used in Plastics Industry:
2,3,6-Trimethylacetophenone is used in the production of plastics and other industrial applications, playing a role in the creation of diverse plastic products.
Safety Precautions:
It is important to handle 2,3,6-Trimethylacetophenone with care as it can cause irritation to the eyes, skin, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 54200-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54200-67:
(7*5)+(6*4)+(5*2)+(4*0)+(3*0)+(2*6)+(1*7)=88
88 % 10 = 8
So 54200-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O/c1-7-5-6-8(2)11(9(7)3)10(4)12/h5-6H,1-4H3
54200-67-8Relevant academic research and scientific papers
Photochemical Reactions. 145th Communication. Carbonyl vs. Epoxyketone Photochemistry: Photolysis of 1,2;3,4-Diepoxy-2,6,6-trimethyl-1-cyclohexyl Methyl Ketone
Phaff, Rox,Bischofberger, Norbert,Mathies, Peter,Petter, Walter,Frei, Bruno,Jeger, Oskar
, p. 1204 - 1216 (2007/10/02)
The synthesis and photolysis of the title compound 3 is described.Irradiation (λ > 280 nm, MeCN) of the di-epoxyketone 3 leads predominantly to γ-H abstraction.Cyclization furnishes the cyclobutanols 22-24, while cleavage gives compound 25, presumably via the allene-oxide intermediate 36.Further, products 27 and 28 are formed by Norrish fragmentation and by initial cleavage of the C(α)-O bond of the oxirane, respectively.The structures of the products 22-25, 27, and 28 were assigned on the basis of the spectral data of the photolysis products of the 13C-labelled diepoxyketone -3 and by X-ray analysis of the compounds 24 and 35, the latter being the p-nitrobenzoate of 22.
