1268631-72-6 Usage
Uses
Used in Pharmaceutical Research:
1-(1,3-Dioxolan-2-yl)-2-(4-methoxyphenyl)ethanone is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential applications in treating a range of medical conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(1,3-Dioxolan-2-yl)-2-(4-methoxyphenyl)ethanone serves as a versatile building block for the creation of complex organic compounds. Its reactivity and structural features make it an ideal candidate for the synthesis of novel molecules with potential applications in various industries.
Used in Fine Chemicals Production:
1-(1,3-Dioxolan-2-yl)-2-(4-methoxyphenyl)ethanone is also employed in the production of fine chemicals, which are high-purity chemicals used in various applications, including pharmaceuticals, agriculture, and materials science. Its unique properties enable the development of high-quality fine chemicals with specific functionalities and applications.
Used in Chemical Research and Development:
1-(1,3-Dioxolan-2-yl)-2-(4-methoxyphenyl)ethanone is utilized in chemical research and development to explore new reaction pathways, develop innovative synthetic methods, and create novel organic compounds with potential applications in various fields, including medicine, materials science, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 1268631-72-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,6,3 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1268631-72:
(9*1)+(8*2)+(7*6)+(6*8)+(5*6)+(4*3)+(3*1)+(2*7)+(1*2)=176
176 % 10 = 6
So 1268631-72-6 is a valid CAS Registry Number.
1268631-72-6Relevant academic research and scientific papers
Chemical synthesis of coelenterazine and its analogs: New route by four segment-couplings
Chou, Chun-Ming,Tung, Yu-Wen,Lin, Meng-I,Chan, Diana,Phakhodee, Wong,Isobe, Minoru
, p. 1323 - 1339 (2013/08/15)
A novel and improved synthetic route includes four segment-couplings toward coelenterazine and its analogs as luminescent molecules. Regio- and chemo-selective cross coupling reactions using palladium catalysts with 5-iodo-3-bromo-2-aminopyrazine have enabled providing various aminopyrazine derivatives having different substituents. The improved synthesis of coelenterazine and its analogs employed advanced condensation with the aminopyrazines using various keto-acetal segments, which resulted in much higher yields to give the final imidazopyrazinone heterocycles than the previous method using keto-aldehydes.
Suzuki-Miyaura coupling for general synthesis of dehydrocoelenterazine applicable for 6-position analogs directing toward bioluminescence studies
Phakhodee, Wong,Toyoda, Mitsuko,Chou, Chun-Ming,Khunnawutmanotham, Nisachon,Isobe, Minoru
experimental part, p. 1150 - 1157 (2011/03/21)
Synthesis of coelenterazine analogs is in recent demand to supply more luminescent compounds with reasonable stability as substrate for the photoprotein manipulated in a living cells or particular organelle. There are limited methods for the synthesis of
