6313-28-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1-(4-chlorophenyl)-1-hydroxy-4,4-dimethylpentan-3-one is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the creation of a wide range of products with different therapeutic and pesticidal properties.
Used as a Flavoring Agent or Fragrance in Consumer Products:
1-(4-chlorophenyl)-1-hydroxy-4,4-dimethylpentan-3-one is also employed in the consumer products industry, where it serves as a flavoring agent or fragrance. Its distinct chemical composition contributes to the development of unique scents and flavors for various applications, enhancing the sensory experience of consumers.
Environmental Considerations:
Due to the presence of the chlorophenyl group, 1-(4-chlorophenyl)-1-hydroxy-4,4-dimethylpentan-3-one may pose environmental risks. Chlorinated compounds are known to be persistent and bioaccumulative, which can lead to potential harm to ecosystems and human health. As a result, special precautions should be taken when handling and disposing of this chemical to minimize its environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 6313-28-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6313-28:
(6*6)+(5*3)+(4*1)+(3*3)+(2*2)+(1*8)=76
76 % 10 = 6
So 6313-28-6 is a valid CAS Registry Number.
6313-28-6Relevant academic research and scientific papers
Solid state aldol reactions of solvated and unsolvated lithium pinacolone enolate aggregates
Pang, Huan,Williard, Paul G.
, (2020/01/13)
We reported the first systematic study of the solid-state aldol reactions of solvated and unsolvated lithium pinacolone enolate with a variety of solid aromatic aldehydes utilizing a mortar and pestle condition in comparison with the simple ball milling condition or tetrahydrofuran (THF) solution condition. In solution, the reactions are highly-selective with the aldol condensation product at room temperature. Under the condition of mortar and pestle, the reactions with unsolvated lithium pinacolone enolate showed the mixture of aldol condensation product and aldol addition product at room temperature. With the usage of solvated lithium pinacolone enolate, higher yields for most substrates were obtained. Furthermore, repeating the reactions under a simple ball billing condition with no other precautions at room temperature, we achieved high selectivity and yield of products for all substrates, indicating the powerful ability and the utility of solid-state, mechanochemical aldol reaction conditions.
