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α-trans-(p-Nitrobenzyliden)-γ-butyrolacton is a synthetic organic compound characterized by a γ-butyrolactone ring with a p-nitrobenzylidene group attached in a trans configuration. This molecule is known for its potential applications in chemical research and as a precursor in the synthesis of various pharmaceuticals and other organic compounds. The p-nitrobenzyliden group introduces a nitro group in the para position relative to the benzylidene linkage, which can significantly influence the reactivity and properties of the molecule. Its chemical structure and functional groups make it a subject of interest in organic chemistry, particularly in the study of reactions involving lactones and aromatic nitro compounds.

52216-84-9

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52216-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52216-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52216-84:
(7*5)+(6*2)+(5*2)+(4*1)+(3*6)+(2*8)+(1*4)=99
99 % 10 = 9
So 52216-84-9 is a valid CAS Registry Number.

52216-84-9Downstream Products

52216-84-9Relevant academic research and scientific papers

Custom synthesis of substituted butenolides, dihydropyranones, and α-E-alkylidenelactones via alkenylalumination

Veeraraghavan Ramachandran,Pratihar, Debarshi,Garner, Garrett,China Raju

, p. 4985 - 4988 (2011/10/08)

Alkenylalumination of aldehydes with [α-(ethoxycarbonyl)-β-(t- butyldimethylsilyloxyalkyl)alkenyl]diisobutylaluminum provides the corresponding α-Z-alkylidene-β′-hydroxy esters, which upon protection and treatment with trifluoroacetic acid lactonizes to f

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