831-29-8 Usage
Uses
Used in Perfumery and Flavoring Industry:
(2,4-Dimethoxyphenyl)acetone is used as a fragrance ingredient and flavoring agent for its strong, sweet, floral odor, enhancing the sensory profiles of various products.
Used in Pharmaceutical Industry:
(2,4-Dimethoxyphenyl)acetone is used as a key precursor in the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Dye Industry:
In the dye industry, (2,4-Dimethoxyphenyl)acetone is utilized as a starting material for the production of different dyes, playing a crucial role in the coloration of textiles and other materials.
Used in Organic Synthesis:
(2,4-Dimethoxyphenyl)acetone is used as a reagent in organic chemical reactions, facilitating the synthesis of a wide range of organic compounds for various applications.
Used in Anti-Aging and Anti-Cancer Research:
(2,4-Dimethoxyphenyl)acetone is used in the production of veratrol, a compound with potential anti-aging and anti-cancer properties, indicating its importance in the development of health and wellness products.
Check Digit Verification of cas no
The CAS Registry Mumber 831-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 831-29:
(5*8)+(4*3)+(3*1)+(2*2)+(1*9)=68
68 % 10 = 8
So 831-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O3/c1-8(12)6-9-4-5-10(13-2)7-11(9)14-3/h4-5,7H,6H2,1-3H3
831-29-8Relevant academic research and scientific papers
Catalytic oxidative 1,2-shift in 1,1′-disubstituted olefins using arene(iodo)sulfonic acid as the precatalyst and oxone as the oxidant
Purohit, Vikram C.,Allwein, Shawn P.,Bakale, Roger P.
, p. 1650 - 1653 (2013/06/27)
An efficient, catalytic hypervalent iodine-mediated oxidative 1,2-shift of 1,1′-disubstituted olefins is described. This methodology provides concise access to homobenzylic ketones with electron-donating substituents. In the case of cyclic systems, this transformation results in ring-expanded β-benzocycloalkanones, which are useful for further elaboration.
Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation
Gaunt,Yu,Spencer
, p. 1844 - 1845 (2007/10/03)
The allylic hydrogen is found to have a dramatic effect on the regioselectivity of the Wacker oxidation, leading to the postulation that an agostic hydrogen or enyl (σ + π) complex helps to stabilise the key intermediate.
A Novel Route to Arylacetones via a Masked α-Acylcarbonium Intermediate
Shatzmiller, Shimon,Lidor, Ramy,Shalom, Eytan,Bahar, Eliezer
, p. 795 - 796 (2007/10/02)
The Ag+ induced aromatic substitution reaction of bromoacetone O-methyloxime is described.
