69313-51-5 Usage
Description
1-(3-acetyl-2,4,5,6-tetramethyl-phenyl)ethanone is a chemical compound characterized by its molecular formula C14H18O. It is a ketone derivative featuring a phenyl group connected to an acetyl group and an ethanone group. 1-(3-acetyl-2,4,5,6-tetramethyl-phenyl)ethanone presents as a yellow to brown crystalline powder with a melting point of 82-84 degrees Celsius. It is recognized for its role in organic synthesis and potential biological and pharmacological properties, such as antioxidant and antimicrobial activities.
Uses
Used in Organic Synthesis:
1-(3-acetyl-2,4,5,6-tetramethyl-phenyl)ethanone is utilized as a reagent in the field of organic synthesis for the preparation of a variety of organic compounds. Its unique structure allows for versatile reactions and the creation of diverse chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(3-acetyl-2,4,5,6-tetramethyl-phenyl)ethanone is investigated for its potential biological and pharmacological activities. Its antioxidant properties make it a candidate for research into treatments for conditions associated with oxidative stress, while its antimicrobial characteristics suggest possible applications in the development of new antibiotics or antifungal agents.
Further research is necessary to explore and confirm the full range of applications and effects of 1-(3-acetyl-2,4,5,6-tetramethyl-phenyl)ethanone across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 69313-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,1 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69313-51:
(7*6)+(6*9)+(5*3)+(4*1)+(3*3)+(2*5)+(1*1)=135
135 % 10 = 5
So 69313-51-5 is a valid CAS Registry Number.
69313-51-5Relevant articles and documents
Positional Reactivity of Acylpolymethylbenzenes in Electrophilic Substitution
Matsuura, Kazunori,Kimura, Yasuo,Takahashi, Hisakazu,Morita, Toshio,Takahashi, Ichiro,et al.
, p. 757 - 765 (2007/10/02)
Friedel-Crafts acylation, bromination, deuteration, and nitration of acetylpentamethylbenzene (APMB), 1-acetyl-2,3,4,6-tetramethylbenzene (ATMB), and 1-benzoyl-2,3,4,6-tetramethylbenzene (BTMB) and the resulting product distribution were investigated.Friedel-Crafts acylation, bromination, and deuteration of APMB and Friedel-Crafts acylation of ATMB gave deacetylation-substitution products.On the other hand, bromination and deuteration of ATMB (or BTMB) and Friedel-Crafts acylation of BTMB gave 5-substituted products.In both cases, the positional reactivities were in accordance with the relative ?-complex stability.Conversely, except for Friedel-Crafts-type nitration, the positional reactivities in the nitration of these substrates were strikingly different from those of the above three reactions.Thus, side-chain functionalization at the 6-methyl group occurred in nitration with fuming nitric acid, depending on the solvents in use.The NMDO calculations and the reaction of APMB with single-electron transfer reagents such as tetranitromethane-hν or cerium(IV) ammonium nitrate suggest that the product distribution in nitration can be explained in terms of a single-electron transfer mechanism.
