1246820-39-2 Usage
Description
Diethyl 2-Ethyl-2-acetamidomalonate-D3, with the CAS number 1246820-39-2, is a white solid compound that plays a significant role in organic synthesis. Its unique chemical structure and properties make it a valuable component in various chemical reactions and processes.
Uses
Used in Organic Synthesis:
Diethyl 2-Ethyl-2-acetamidomalonate-D3 is used as a synthetic intermediate for the production of various organic compounds. Its reactivity and versatility allow it to be incorporated into a wide range of chemical reactions, facilitating the synthesis of complex molecules and pharmaceuticals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Diethyl 2-Ethyl-2-acetamidomalonate-D3 is used as a key building block in the development of new drugs and therapeutic agents. Its ability to participate in various chemical reactions makes it an essential component in the synthesis of novel compounds with potential medicinal properties.
Used in Chemical Research:
Diethyl 2-Ethyl-2-acetamidomalonate-D3 is also utilized in chemical research to study the mechanisms of various organic reactions and to develop new synthetic methodologies. Its unique properties and reactivity make it a valuable tool for understanding and optimizing chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1246820-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,8,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1246820-39:
(9*1)+(8*2)+(7*4)+(6*6)+(5*8)+(4*2)+(3*0)+(2*3)+(1*9)=152
152 % 10 = 2
So 1246820-39-2 is a valid CAS Registry Number.
1246820-39-2Relevant articles and documents
Pyrrolizidine alkaloid biosynthesis. Incorporation of 2-aminobutanoic acid labelled with 13C or 2H into the senecic acid portion of rosmarinine and senecionine
Stirling, Iain R.,Freer, Isabel K. A.,Robins, David J.
, p. 677 - 680 (1997)
(±)-[3,4-13C2]-2-Aminobutanoic acid 10 and (±)-[3,4-2H5]-2-aminobutanoic acid 11 are synthesized by alkylating diethyl acetamidomalonate with labelled ethyl iodide followed by acid hydrolysis. These compounds are used to obtain complete labelling patterns for the first time in a necic acid by studying the pyrrolizidine alkaloids rosmarinine 3 and senecionine 1 using NMR spectroscopy. The senecic acid portion 12 of both alkaloids shows equal incorporation of [3,4-13C2]-2-aminobutanoic acid 10 into the two C5 halves of the C10 acid consistent with formation of senecic acid via two molecules of isoleucine. After feeding [3,4-2H5]-2-aminobutanoic acid 11, retention of 2H at C-13 and C-20 of both alkaloids 13 confirms that the biosynthesis does not involve keto intermediates at these carbon atoms.
