6175-45-7 Usage
Description
2,2-Diethoxyacetophenone is a clear yellow to salmon liquid that serves as an effective photoinitiator for UV-curable acrylate-based coatings, adhesives, and inks. Its chemical properties make it particularly useful in UV-curable systems, especially in applications where non-yellowing is crucial.
Uses
Used in Coatings Industry:
2,2-Diethoxyacetophenone is used as a photoinitiator for UV-curable acrylate-based coatings, providing efficient curing and non-yellowing properties, which are essential for maintaining the appearance and quality of the final product.
Used in Adhesives Industry:
In the adhesives industry, 2,2-Diethoxyacetophenone is utilized as a photoinitiator for UV-curable acrylate-based adhesives, ensuring rapid curing and strong bonding capabilities without compromising the color or appearance of the materials being bonded.
Used in Inks Industry:
2,2-Diethoxyacetophenone is employed as a photoinitiator in the production of UV-curable acrylate-based inks, offering non-yellowing properties and improved shelf life, which are vital for maintaining color stability and print quality in various applications.
Used in Pigmented Inks:
2,2-Diethoxyacetophenone is used as a photoinitiator for pigmented inks, where its non-yellowing properties and ability to enhance shelf life and color stability make it an ideal choice for applications requiring long-lasting and vibrant colors.
Check Digit Verification of cas no
The CAS Registry Mumber 6175-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6175-45:
(6*6)+(5*1)+(4*7)+(3*5)+(2*4)+(1*5)=97
97 % 10 = 7
So 6175-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O2.C6H14O2.C4H10/c9-6-8(10)7-4-2-1-3-5-7;1-4-7-6(3)8-5-2;1-3-4-2/h1-6H;6H,4-5H2,1-3H3;3-4H2,1-2H3
6175-45-7Relevant articles and documents
Modular Synthesis of α-Substituted Alkenyl Acetals by a Palladium-Catalyzed Suzuki Reaction of α-Haloalkenyl Acetals with Organoboranes
Zhang, Li
, p. 723 - 727 (2021/02/26)
A modular and straightforward synthetic strategy for the preparation of α-substituted alkenyl acetals has been developed. α-Haloalkenyl acetals react smoothly with (het)aryl boronic acids, aryl boronates, or B-Alkyl-9-borabicyclo[3.3.1]nonanes through Pd-catalyzed Suzuki cross-coupling under mild conditions with good to high yields. This protocol features a broad substrate scope and good functional-group compatibility, and is easily scaled up.
Synergistic Catalysis of Se and Cu for the Activation of α-H of Methyl Ketones with Molecular Oxygen/Alcohol to Produce α-Keto Acetals?
Chen, Chao,Cao, Zhicheng,Zhang, Xu,Li, Yiming,Yu, Lei,Jiang, Xuefeng
, p. 1045 - 1051 (2020/06/30)
Selenium and copper synergistically catalyzed the oxidation/alkoxylation of methyl ketones to synthesize α-keto acetals directly. Using O2 as oxidant and alcohol as solvent and alkoxylation reagent, the reaction is practical from industrial viewpoint. Mechanistic studies revealed that copper promoted the oxidation of organoselenium intermediates with O2 to allow the key rearrangement and selenoxide syn-elimination regenerating the catalytically active organoselenium species.
Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents
Malmedy, Florence,Wirth, Thomas
supporting information, p. 16072 - 16077 (2016/10/30)
The first stereoselective version of an iodine(III)-mediated rearrangement of arylketones in the presence of orthoesters is described. The reaction products, α-arylated esters, are very useful intermediates in the synthesis of bioactive compounds such as ibuprofen. With chiral lactic acid-based iodine(III) reagents product selectivities of up to 73 % ee have been achieved.