3883-57-6 Usage
Uses
Used in Electronics and Semiconductor Industries:
Cyclotene acetate is utilized as a key material in these industries due to its high thermal stability and chemical resistance, which are essential for manufacturing processes involving sensitive electronic components and semiconductor devices.
Used in Plastics Production:
It serves as a vital ingredient in the creation of various types of plastics, leveraging its structural integrity and resistance to heat and chemicals to produce durable and reliable plastic products.
Used in Adhesives:
Cyclotene acetate is employed as a component in adhesive formulations, where its bonding properties and resistance to environmental factors contribute to the performance and longevity of the adhesives.
Used in Coatings:
CYCLOTENE ACETATE is used in the development of coatings that require high durability and resistance to various environmental stresses, such as temperature fluctuations and chemical exposure, ensuring the protection and longevity of coated surfaces.
Used in Photoresist Formulation for Microelectronics:
Cyclotene acetate plays a crucial role in the production of photoresists, which are indispensable in the patterning processes of microelectronics manufacturing, allowing for the creation of intricate and precise electronic components.
Check Digit Verification of cas no
The CAS Registry Mumber 3883-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3883-57:
(6*3)+(5*8)+(4*8)+(3*3)+(2*5)+(1*7)=116
116 % 10 = 6
So 3883-57-6 is a valid CAS Registry Number.
InChI:InChI=1S/C8H10O3/c1-5-7(10)3-4-8(5)11-6(2)9/h3-4H2,1-2H3
3883-57-6Relevant academic research and scientific papers
The Synthesis of 4-Prop-2-enyl Substituted cyclopentane-1,3-dione Enol Esters, and an Investigation of their Structures by N.m.r. Spectroscopy
Barker, Andrew J.,Pattenden, Gerald
, p. 1885 - 1891 (2007/10/02)
Alkylations of dianions derived from cyclopentane-1,3-dione and 2-methylcyclopentane-1,3-dione are shown to provide an expeditious route to the corresponding 4-alkylated derivatives (9).Unsymmetrical 4,5-disubstituted cyclopentane-1,3-diones (11) are more easily obtained by isomerisation of the corresponding 4-hydroxycyclopent-2-enones (10) in the presence of methanolic sodium methoxide.Proton and carbon-13 n.m.r. data establish that the 4-prop-2-enyl substituted cyclopentane-1,3-diones (9a-d, R = H, Me) and (11a-c) are fully enolised in solution, and that the two enolic forms are undergoing rapid tautomerism.N.m.r. data also show that whereas the 2-methyl substituted diones (9a, b, d; R = Me) produce single enol acetates on treatment with acetic anhydride-sodium acetate, the analogues (9a, c, d; R = H) and (11a-c) instead lead to mixtures of isomeric enol acetates .In the case of the 4,5-disubstituted enol acetates (35), (36), and (41)->(44), the C-4, C-5 substituents are shown to have an anti-stereochemical relationship to one another.
