16695-59-3 Usage
Uses
Used in Photopolymerization Applications:
2,2-DIMETHOXY-1-PIPERIDINO-1-ETHANONE is used as a photoinitiator for the polymerization of resins, particularly in the development of coatings, inks, and adhesives that require curing by exposure to light. Its effectiveness in initiating the polymerization process under light exposure makes it a valuable component in these applications.
Used in Coating Industry:
2,2-DIMETHOXY-1-PIPERIDINO-1-ETHANONE is used as a photoinitiator in the formulation of light-curable coatings. Its ability to initiate polymerization upon light exposure allows for the creation of durable and high-quality coatings that are essential in various industries.
Used in Ink Industry:
In the ink industry, 2,2-DIMETHOXY-1-PIPERIDINO-1-ETHANONE is used as a photoinitiator for the production of UV-curable inks. Its role in the curing process ensures that the inks adhere well to various surfaces, providing a long-lasting and vibrant print.
Used in Adhesive Industry:
2,2-DIMETHOXY-1-PIPERIDINO-1-ETHANONE is used as a photoinitiator in the formulation of light-curable adhesives. Its ability to initiate rapid curing upon exposure to light makes it an essential component in the production of adhesives that require quick setting and strong bonding.
Used in Electronic Components Manufacturing:
2,2-DIMETHOXY-1-PIPERIDINO-1-ETHANONE is used as a photoinitiator in the manufacturing of electronic components, where precise and quick curing of materials is crucial for the production of reliable and high-performance devices.
Used in Printing Materials Production:
In the production of printing materials, 2,2-DIMETHOXY-1-PIPERIDINO-1-ETHANONE is used as a photoinitiator to facilitate the curing of inks and coatings. Its role in the curing process ensures that the printed materials have a consistent and high-quality finish.
Check Digit Verification of cas no
The CAS Registry Mumber 16695-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,9 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16695-59:
(7*1)+(6*6)+(5*6)+(4*9)+(3*5)+(2*5)+(1*9)=143
143 % 10 = 3
So 16695-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO3/c1-12-9(13-2)8(11)10-6-4-3-5-7-10/h9H,3-7H2,1-2H3
16695-59-3Relevant academic research and scientific papers
REACTIVIDAD DE ENAMINAS TERCIARIAS DE DERIVADOS CICLICOS Y DE CADENA ABIERTA DEL ACIDO 3,4-DIOXOBUTANOICO
Ancos, B. de,Farina, F.,Maestro, M. C.,Martin, M. R.
, p. 132 - 141 (2007/10/02)
Enaminoester 1a and enaminofuranone 2 with iodomethane, 2-chloro-1,3-dithiane and phenyldiazonium tetrafluoroborate afford the products resulting from electrophilic attack on the C-α to the carbonyl group.However, acyl chlorides with 1a yield O-acylated products.The above reactives and 1a give the corresponding products of enamino group hydrolysis.Enamines 1a and 1b react with dichlorocarbene, generated in phase transfer conditions, to yield chlorofuranones 17a and 17b dimethoxyacetamides 18a and 18b . p-Nitrophenylazide affords 1,2,3-triazol 20 in good yield by reaction with enaminoester 2; but when reacts with 2 gives in small amount the azoderivative 21.It is noteworthy that in the above cycloaddition reactions, the open-chained enaminoester 1a is much more reactive than the enaminofuranone 2.Palabras clave: Enaminoester, enaminolactona, alquilacion, acilacion, cicloadicion, diclorocarbeno, triazol.
