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1-(4-Methoxyphenyl)-4,5-dioxo-2-phenyl-3-pyrrolidinecarboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

401941-23-9

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401941-23-9 Usage

Explanation

The compound's full name, which describes its structure and components.

Explanation

An alternative name for the compound, often used in scientific literature and research.

Explanation

The compound consists of a pyrrolidine ring (a five-membered ring with one nitrogen atom) and a phenyl group (a six-membered ring with alternating single and double carbon-carbon bonds).

Explanation

The compound is derived from a pyrrolidinecarboxylic acid by forming an ester bond with an ethyl group.

Explanation

The compound contains an ester functional group (formed by the reaction of an acid and an alcohol), a phenyl group, and a methoxy group (an oxygen atom bonded to a methyl group).

Explanation

The compound is used in the synthesis of other organic compounds and is also studied for its potential applications in the pharmaceutical industry.

Explanation

The compound may have pharmacological properties, which could be useful in the development of new drugs or as a reference compound in scientific studies.

Explanation

The compound's utility and effectiveness are determined by the specific context in which it is being used, such as the target disease or the desired outcome of the research.

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule, which is used to calculate the mass of a specific quantity of the compound.

Structure

Pyrrolidine ring and a phenyl group

Type

Ester derivative

Functional Groups

Ester, phenyl, and methoxy groups

Applications

Organic synthesis and pharmaceutical research

Potential Properties

Pharmacological properties

Context-Dependent Uses

Specific uses and effects depend on the research or application goals

Molecular Weight

Approximately 341.37 g/mol

Check Digit Verification of cas no

The CAS Registry Mumber 401941-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,9,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 401941-23:
(8*4)+(7*0)+(6*1)+(5*9)+(4*4)+(3*1)+(2*2)+(1*3)=109
109 % 10 = 9
So 401941-23-9 is a valid CAS Registry Number.

401941-23-9Downstream Products

401941-23-9Relevant academic research and scientific papers

A Br?nsted acid-catalyzed multicomponent reaction for the synthesis of highly functionalized γ-lactam derivatives

Corte, Xabier del,de Marigorta, Edorta Martinez,Palacios, Francisco,Vicario, Javier

, (2019)

Br?nsted acids catalyze a multicomponent reaction of benzaldehyde with amines and diethyl acetylenedicarboxylate to afford highly functionalized γ-lactam derivatives. The reaction consists of a Mannich reaction of an enamine to an imine, both generated in situ, promoted by a phosphoric acid catalyst and a subsequent intramolecular cyclization. The hydrolysis of the cyclic enamine substrate can provide enol derivatives and, moreover, a second attack of the amine on the carboxylate can afford amide derivatives. An optimization of the reaction conditions is presented in order to obtain selectively cyclic enamines that can afford the enol species after selective hydrolysis.

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