50427-65-1 Usage
Uses
Used in Chemical Synthesis:
METHYL 2-FORMYL-3-OXO-PROPIONATE is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure and reactive properties make it a valuable building block in the preparation of complex molecules.
Used in Pharmaceutical Industry:
METHYL 2-FORMYL-3-OXO-PROPIONATE is used as a key component in the development of pharmaceuticals. Its reactivity allows for the creation of new drug candidates with potential therapeutic applications.
Used in Research and Development:
METHYL 2-FORMYL-3-OXO-PROPIONATE is used as a research compound for studying the properties and reactions of alpha keto acids and their derivatives. This helps in understanding the fundamental chemistry and potential applications of these compounds.
Used in Material Science:
METHYL 2-FORMYL-3-OXO-PROPIONATE is used as a precursor in the synthesis of advanced materials, such as polymers and composites, with specific properties tailored for various applications. Its versatility in chemical reactions enables the development of novel materials with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 50427-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50427-65:
(7*5)+(6*0)+(5*4)+(4*2)+(3*7)+(2*6)+(1*5)=101
101 % 10 = 1
So 50427-65-1 is a valid CAS Registry Number.
50427-65-1Relevant academic research and scientific papers
Synthetic access to poly-substituted 11H-pyrido[3,2-a]carbazoles, A dna-intercalating ellipticine related structure, and their antiproliferative activity
Wu, Ming-Yu,Shaban, Elkhabiry,Switalska, Marta,Wang, Ning,Shimoda, Miho,Mizutani, Yusuke,Yoshida, Megumi,Mei, Zhen-Wu,Kawafuchi, Hiroyuki,Nokami, Junzo,Wietrzyk, Joanna,Yu, Xiao-Qi,Inokuchi, Tsutomu
, p. 1427 - 1440 (2014/07/07)
The facile procedure for the synthesis of the 11H-pyrido[3,2-a]carbazole structure involving the Fischer indole cyclization on tetrahydroquinolinones, available from enaminones and methyl 2-formyl-3-oxopropanoate, followed by the aromatization of the resulting 5,6-dihydro derivatives is described. This method allows for the introduction of substituents at C2, C6, and C8 to the scaffold by choice of the starting materials. In the biological testing, introduction of the phenyl group at C6 is significantly effective to improve the antiproliferative activity.
