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1-(2,4-DIMETHYL-PHENYL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID is a chemical compound belonging to the class of pyrrolidine carboxylic acids. It is a small molecule characterized by a molecular formula of C13H15NO3 and a molecular weight of 233.26 g/mol. 1-(2,4-DIMETHYL-PHENYL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID is recognized for its pharmacological activities and is utilized in organic synthesis and pharmaceutical research, playing a significant role in drug design and lead optimization for a variety of diseases and conditions. Its unique properties and applications render it a valuable and important chemical in the realm of drug discovery and development.

133748-22-8

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133748-22-8 Usage

Uses

Used in Pharmaceutical Research:
1-(2,4-DIMETHYL-PHENYL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID is used as a research compound for its pharmacological activities, contributing to the advancement of drug discovery and development. It aids in the design and optimization of lead compounds for various diseases and conditions, enhancing the potential for new therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2,4-DIMETHYL-PHENYL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID is used as a key intermediate or building block in the synthesis of more complex organic molecules. Its unique structure and reactivity make it a valuable component in the creation of novel compounds with potential applications in various industries.
Used in Drug Design:
1-(2,4-DIMETHYL-PHENYL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID is employed as a structural element in drug design, where its properties can be leveraged to develop new pharmaceuticals with improved efficacy, selectivity, and safety profiles. Its incorporation into drug candidates can lead to the discovery of innovative treatments for a range of medical conditions.
Used in Lead Optimization:
In the process of lead optimization, 1-(2,4-DIMETHYL-PHENYL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID is utilized to refine and improve the properties of potential drug candidates. Its versatility allows for the fine-tuning of pharmacokinetic and pharmacodynamic properties, increasing the likelihood of successful drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 133748-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,4 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133748-22:
(8*1)+(7*3)+(6*3)+(5*7)+(4*4)+(3*8)+(2*2)+(1*2)=128
128 % 10 = 8
So 133748-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3/c1-8-3-4-11(9(2)5-8)14-7-10(13(16)17)6-12(14)15/h3-5,10H,6-7H2,1-2H3,(H,16,17)/p-1/t10-/m1/s1

133748-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-dimethylphenyl)-5-oxopyrrolidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Pyrrolidinecarboxylicacid,1-(2,4-dimethylphenyl)-5-oxo

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:133748-22-8 SDS

133748-22-8Upstream product

133748-22-8Relevant academic research and scientific papers

Phenylcarboxylic acid derivatives having hetero ring

-

, (2008/06/13)

Phenylcarboxylic acid derivatives having a hetero ring in the substituent of the formula: STR1 wherein R1 is halogen, alkyl, cycloalkyl, hydroxy, alkoxy, phenoxy which has a substituent selected from halogen and alkyl, carboxyl, alkylsulfonyloxy, phenylsulfonyloxy optionally substituted by halogen, alkylsulfonyloxyalkoxy, amino, alkanoylamino, benzoylamino, alkenyloxy, phenylalkoxyalkoxy, hydroxyalkoxy, phenylalkoxy having optionally 1 to 3 substituents selected from halogen, alkyl and alkoxy, halogenoalkyl, cycloalkyloxy optionally substituted by hydroxy, alkoxy substituted by cycloalkyl having optionally hydroxy substituent, imidazolylalkyl or imidazolylalkoxy; k is 0 or 1 to 3; or (R1)k is alkylenedioxy; A is alkylene or alkylenoxy; l is 0 or 1; B is methylene or carbonyl; m is 0 or 1; D is alkylene; E is alkylene or alkenylene; n is 0 or 1; and R2 is hydrogen or alkyl, or a salt thereof, which have fatty acid synthesis-inhibitory activity, cholesterol synthesis-inhibitory activity and are useful as antilipidemic agent, prophylactic and treating agent of arteriosclerosis, prophylactic and treating agent of obesity, antidiabetics.

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