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Benzenepropanoic acid, b-hydroxy-2-nitro-, ethyl ester, also known as 2-nitro-3-phenyllactic acid ethyl ester, is an organic compound with the chemical formula C11H13NO5. It is a derivative of benzenepropanoic acid, featuring a hydroxyl group at the beta position, a nitro group at the 2-position, and an ethyl ester group. Benzenepropanoic acid, b-hydroxy-2-nitro-, ethyl ester is characterized by its aromatic structure, which includes a benzene ring attached to a propanoic acid chain. The presence of the nitro group and the hydroxyl group at specific positions on the molecule can influence its reactivity and properties. It is used in the synthesis of various pharmaceuticals and chemical compounds due to its unique structure and functional groups.

6925-95-7

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6925-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6925-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6925-95:
(6*6)+(5*9)+(4*2)+(3*5)+(2*9)+(1*5)=127
127 % 10 = 7
So 6925-95-7 is a valid CAS Registry Number.

6925-95-7Downstream Products

6925-95-7Relevant academic research and scientific papers

Environmentally benign metal-free decarboxylative aldol and Mannich reactions

Baudoux, Jerome,Lefebvre, Pierre,Legay, Remi,Lasne, Marie-Claire,Rouden, Jacques

experimental part, p. 252 - 259 (2011/03/18)

Aiming at the development of green and efficient C-C bond formations (aldol and Mannich reactions), the decarboxylative nucleophilic addition of malonic acid half ester to imines or aldehydes under mild metal-free conditions was studied. A careful control of the temperature and the appropriate choice of the organic base allowed us to obtain β-amino esters or β-hydroxy esters including α-substituted and α,α-disubstituted ones in moderate to excellent yields. 1H NMR monitoring of the reaction unveiled two distinct mechanisms depending on the hemimalonate used. With the unsubstituted substrate, a carboxylic acid intermediate was isolated upon acid quench resulting from the nucleophilic addition of the putative enol carboxylate anion of the hemimalonate to imines/aldehydes before CO2 loss. With substituted hemimalonates, the reaction likely involved an enolate which then added to imines/aldehydes or was competitively protonated. According to the base used, the reaction can be carried out either under solvent free-conditions or in an ionic liquid under mild conditions.

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