20669-05-0 Usage
Uses
Used in the Paint and Coating Industry:
2,2,4,4-tetramethylhexan-3-one is used as a solvent for its ability to dissolve a wide range of substances, which is crucial in the production of lacquers, paints, and coatings. Its solvent properties enhance the performance and application of these products.
Used in the Food and Cosmetic Industries:
In the food and cosmetic sectors, 2,2,4,4-tetramethylhexan-3-one is utilized as a flavoring agent and fragrance. Its sweet, fruity odor makes it suitable for adding pleasant scents and tastes to various products.
Used in the Chemical and Pharmaceutical Industries:
2,2,4,4-tetramethylhexan-3-one serves as an intermediate in the synthesis of other chemicals and pharmaceuticals. Its role in chemical reactions is essential for producing a variety of end products that have different applications in medicine and other fields.
Safety Considerations:
While 2,2,4,4-tetramethylhexan-3-one is considered to have low toxicity, it is important to handle and store it with care. Prolonged or repeated exposure may lead to irritation of the skin, eyes, and respiratory system, necessitating proper safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 20669-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20669-05:
(7*2)+(6*0)+(5*6)+(4*6)+(3*9)+(2*0)+(1*5)=100
100 % 10 = 0
So 20669-05-0 is a valid CAS Registry Number.
20669-05-0Relevant academic research and scientific papers
CONDENSATION DES ORGANOMAGNESIENS SUR LES CHLORUSES D'ACIDE DANS LE TETRAHYDROFURANNE A BASSE TEMPERATURE
Dubois, Jacques-Emile,Lion, Claude,Arouisse, Abdelmajid
, p. 1083 - 1088 (2007/10/02)
The condensation of a Grignard reagents with hindered acid chlorides in THF at low temperature, yields ketones which are generally difficult to obtain and avoids the side reaction caused with a CuCl catalyst.Applied to unsaturated Grignard reagents and acid chlorides, this method also yields unsaturated ketones, such as the Artemisia ketone.
