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2H-Pyrrol-2-one, 4-ethoxy-1,5-dihydro-3-(1-methoxyethenyl)-1-methyl-(9CI) is a complex organic compound with the chemical formula C9H15NO3. It belongs to the class of pyrrole derivatives, which are heterocyclic compounds containing a nitrogen atom in the ring structure. This specific compound features a pyrrole ring with a 1-methyl group, a 3-(1-methoxyethenyl) substituent, and a 4-ethoxy group. The presence of these functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its complex structure, it is essential to handle 2H-Pyrrol-2-one,4-ethoxy-1,5-dihydro-3-(1-methoxyethenyl)-1-methyl-(9CI) with care and follow proper safety protocols during synthesis and use.

651322-77-9

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651322-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651322-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,3,2 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 651322-77:
(8*6)+(7*5)+(6*1)+(5*3)+(4*2)+(3*2)+(2*7)+(1*7)=139
139 % 10 = 9
So 651322-77-9 is a valid CAS Registry Number.

651322-77-9Downstream Products

651322-77-9Relevant academic research and scientific papers

Studies Directed toward the Total Synthesis of Lactonamycin: Control of the Sense of Cycloaddition of a Quinone through Directed Intramolecular Catalysis

Cox, Christopher D.,Siu, Tony,Danishefsky, Samuel J.

, p. 5625 - 5629 (2007/10/03)

The rapid assembly of the ABCD tetracyclic ring system of lactonamycin involved the strong-base-induced regioselective Diels-Alder reaction of 1 and 2 to form advanced precursor 3. Regiochemical control results from the suitably positioned hydroxy group,

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