19549-83-8 Usage
Uses
Used in the Food Industry:
2,6-DIMETHYL-3-HEPTANONE is used as a flavoring agent for its distinctive sweet and floral scent, enhancing the taste and aroma of various food products.
Used in the Cosmetic and Perfume Industry:
In the cosmetic and perfume industry, 2,6-DIMETHYL-3-HEPTANONE serves as a fragrance component, leveraging its pleasant odor to contribute to the overall scent profile of products.
Used in the Paint and Coating Industry:
2,6-DIMETHYL-3-HEPTANONE is utilized as a solvent in the paint, resin, and lacquer industry, where it aids in the application process and improves the flow and drying characteristics of these materials.
Used in the Pharmaceutical Industry:
Within the pharmaceutical sector, 2,6-DIMETHYL-3-HEPTANONE is employed as an intermediate in the synthesis of a range of compounds, playing a crucial role in the development of various medications.
Used in the Agricultural Industry:
In agriculture, 2,6-DIMETHYL-3-HEPTANONE finds use as an intermediate in the synthesis of compounds that contribute to the development of agricultural chemicals, supporting crop protection and enhancement efforts.
It is important to handle 2,6-DIMETHYL-3-HEPTANONE with care due to its potential hazards, such as harmful effects if ingested, the possibility of causing skin and eye irritation, and the risk of harm through inhalation. Proper safety measures should be taken to mitigate these risks during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19549-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,4 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19549-83:
(7*1)+(6*9)+(5*5)+(4*4)+(3*9)+(2*8)+(1*3)=148
148 % 10 = 8
So 19549-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-7(2)5-6-9(10)8(3)4/h7-8H,5-6H2,1-4H3
19549-83-8Relevant academic research and scientific papers
NOVEL THIOPHENE DERIVATIVES AS S1P1/EDG1 RECEPTOR AGONISTS
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Page/Page column 36, (2010/11/28)
The invention relates to thiophene derivatives of formula (I) / their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents wherein: A represents *-CO-CH=CH-, *-CO-CH2CH2-, *-CO-CH2-NH-, wherein the sterisks indicate the bond that is linked to the thiophene group of Formula (I) , and R1-R3 are as defined in the claims.
The Willgerodt-Kindler Reactions. 6. Isomerization of the Carbonyl Group in Alkanones and Cycloalkanones
Carmack, Marvin,Behforouz, Mohammad,Berchtold, Glenn A.,Berkowitz, Samuel M.,Wiesler, Donald,Barone, Ralph
, p. 1305 - 1318 (2007/10/02)
The most unusual feature of the Willgerodt-Kindler Reactions is the facile isomerization of the carbonyl function along a chain of unbranched methylene groups, or around a cycloaliphatic ring containing several connected methylene groups.We have demonstrated that the first step in the Kindler process is the formation of enamines by reaction of the carbonyl function with secondary aliphatic amines, followed by reaction of the enamine with certain sulfur-amine catalysts to form reactive heterocyclic sulfur intermediates that facilitate the elimination-readdition of the amines reversibly along the chain.It was shown that compounds of the type R2N-S-S-NR2 are effective catalysts but not compounds of the type R2N-S-NR2.Some cyclohexanone derivatives undergo aromatization, with anomalous results in certain cases.
