128445-74-9 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-2-(ethoxymethylene)cyclohexanone is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, making it a valuable asset in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (Z)-2-(ethoxymethylene)cyclohexanone serves as a key component in the production of various agrochemicals. Its versatility in organic synthesis enables the development of effective products for agricultural applications.
Used in Fine Chemicals:
(Z)-2-(ethoxymethylene)cyclohexanone is utilized as a building block in the synthesis of fine chemicals. Its functional group and structural properties make it suitable for creating high-quality specialty chemicals used in various industries.
Used in Fragrance and Flavoring Industry:
(Z)-2-(ethoxymethylene)cyclohexanone is used as a reagent in the production of fragrances and flavoring agents. The unique structure and functional group of (Z)-2-(ethoxymethylene)cyclohexanone contribute to the creation of distinct and appealing scents and tastes.
Used in Materials and Polymer Development:
(Z)-2-(ethoxymethylene)cyclohexanone has potential applications in the development of materials and polymers. Its structural properties make it a promising candidate for the synthesis of novel materials with specific characteristics, further expanding its utility in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 128445-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,4,4 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128445-74:
(8*1)+(7*2)+(6*8)+(5*4)+(4*4)+(3*5)+(2*7)+(1*4)=139
139 % 10 = 9
So 128445-74-9 is a valid CAS Registry Number.
128445-74-9Relevant academic research and scientific papers
Chemistry of enol ethers. LI. Reaction of vinyl silyl ethers with orthoformic esters
Makin, S. M.,Kruglikova, R. I.,Popova, T. P.,Tagirov, T. K.
, p. 630 - 634 (2007/10/02)
The silyl ethers of enolic forms of ketones react with orthoformates in the presence of zinc chloride at catalyst to form β-ketoacetals.The analogous reaction with the silyl ethers of enolic forms of aldehydes leads to the formation of the tetraacetals of 1,3-dialdehydes.
