10338-85-9 Usage
Uses
Used in Organic Synthesis:
2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one is used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for further chemical reactions and modifications, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one is used as a chiral building block for the production of pharmaceuticals. Its chiral properties enable the creation of enantiomerically pure compounds, which are essential for the development of effective and safe medications.
Used in Agrochemical Industry:
2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one is also utilized in the agrochemical industry as a chiral building block for the synthesis of agrochemicals. Its chiral nature allows for the development of targeted and efficient pesticides and other agricultural chemicals.
Used as Insecticide and Fungicide:
Due to its insecticidal and fungicidal properties, 2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one is used as a pesticide in agriculture and horticulture. Its ability to control pests and diseases helps protect crops and maintain high yields.
Used in Material Science:
2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one has potential applications in the development of new materials and chemical processes. Its unique structure and properties can be harnessed to create innovative materials with specific characteristics, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 10338-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,3 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10338-85:
(7*1)+(6*0)+(5*3)+(4*3)+(3*8)+(2*8)+(1*5)=79
79 % 10 = 9
So 10338-85-9 is a valid CAS Registry Number.
10338-85-9Relevant academic research and scientific papers
Lewis Acid Catalysis of Ene Addition of Chloral and Bromal to Olefins; Product Studies
Benner, Jill P.,Gill, G. Bryon,Parrott, Stephen J.,Wallace, Brian
, p. 291 - 313 (2007/10/02)
The addition of chloral and bromal to a variety of alkyl-substituted alkenes has been investigated.The effect of the reaction of varying the Lewis acid catalyst and the structure of substrate have been studied.Anhydrous AlCl3 was found to be most effective catalyst, and ene-type adducts were the major products in most cases.Side reactions were observed with the less reactive systems leading, variously, to the formation of trihalogenoketones, hydrohalogenated ene adducts, and cyclic ethers.Conditions for optimising the yield of ene adducts were established in some cases.The trihalogenoketone by-products can be conveniently removed by a Grignard-type reaction.
