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1-(4-methylphenyl)-2-oxopyrrolidine-3-carboxylic acid is a chemical compound with a molecular formula C13H15NO3. It is a white to off-white crystalline powder that is soluble in water and organic solvents. 1-(4-methylphenyl)-2-oxopyrrolidine-3-carboxylic acid is a derivative of pyrrolidine and is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It has the potential for antibacterial and antiviral activity and may have applications in the development of new drugs. Additionally, it is used in research and development as a reagent and intermediate in organic synthesis. 1-(4-methylphenyl)-2-oxopyrrolidine-3-carboxylic acid is typically handled and used in a laboratory setting with proper safety precautions in place.

618070-29-4

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618070-29-4 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-methylphenyl)-2-oxopyrrolidine-3-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals. Its potential for antibacterial and antiviral activity makes it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
1-(4-methylphenyl)-2-oxopyrrolidine-3-carboxylic acid is used as a building block for the synthesis of various agrochemicals. Its potential applications in this industry contribute to the development of effective and innovative products for agricultural use.
Used in Research and Development:
1-(4-methylphenyl)-2-oxopyrrolidine-3-carboxylic acid is used as a reagent and intermediate in organic synthesis. Its versatility in chemical reactions and potential applications make it a valuable tool for researchers and scientists working in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 618070-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,8,0,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 618070-29:
(8*6)+(7*1)+(6*8)+(5*0)+(4*7)+(3*0)+(2*2)+(1*9)=144
144 % 10 = 4
So 618070-29-4 is a valid CAS Registry Number.

618070-29-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Methylphenyl)-2-oxo-3-pyrrolidinecarboxylic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:618070-29-4 SDS

618070-29-4Relevant academic research and scientific papers

INDOLE AMIDE DERIVATIVES AND RELATED COMPOUNDS FOR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES

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Page/Page column 174, (2010/12/29)

This invention provides novel compounds and the novel compounds for use as a medicine, more in particular for the prevention or treatment of neurodegenerative disorders, more specifically certain neurological disorders, such as disorders collectively known as tauopathies, and disorders characterised by cytotoxic α-synuclein amyloidogenesis. The present invention also relates to the use of said novel compounds for the manufacture of medicaments useful for treating such neurodegenerative disorders. The present invention further relates to pharmaceutical compositions including said novel compounds and to methods for the preparation of said novel compounds.

Sodium borohydride-iodine mediated reduction of γ-lactam carboxylic acids followed by DDQ mediated oxidative aromatisation: a simple approach towards N-aryl-formylpyrroles and 1,3-diaryl-formylpyrroles

Haldar, Pranab,Barman, Gopa,Ray, Jayanta K.

, p. 3049 - 3056 (2007/10/03)

A simple methodology for the conversion of substituted N-aryl-γ-lactam 2/3-carboxylic acids to substituted N-aryl-2/3-formyl-pyrroles has been developed. Several N-aryl-γ-lactam 2/3-carboxylic acids were reduced to substituted (N-aryl-pyrroliden-2/3-yl)-m

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