133747-74-7

Basic information

• Product Name: 1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID
• Synonyms: 1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID;5-oxo-1-(4-propylphenyl)-3-Pyrrolidinecarboxylic acid
• CAS NO: 133747-74-7
• Molecular Formula: C₁₄H₁₇NO₃
• Molecular Weight: 247.29
• Mol File: 133747-74-7.mol

Chemical Properties

• Boiling Point: 518.1 °C at 760 mmHg
• Flash Point: 267.2 °C
• Appearance: /
• Density: 1.224 g/cm³
• CAS DataBase Reference: 1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID(133747-74-7)
• EPA Substance Registry System: 1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID(133747-74-7)

Safety Data

• Hazardous Substances Data: 133747-74-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of molecules with potential therapeutic properties, making it valuable in medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-PROPYLPHENYL)-5-OXOPYRROLIDINE-3-CARBOXYLICACID is utilized as a building block for constructing various organic molecules. Its presence in these molecules can introduce new functional groups and chemical properties, broadening the scope of possible applications in different chemical and material sciences.

Upstream product

• 97-65-4 2-methylenesuccinic acid 
• 2696-84-6 4-propylaniline 

Downstream Products

• 133747-77-0 Methyl 4-[1-(4-n-propylphenyl)-2-pyrrolidon-4-yl]methoxybenzoate 
• 1027256-33-2 Methanesulfonic acid 5-oxo-1-(4-propyl-phenyl)-pyrrolidin-3-ylmethyl ester 
• 133747-76-9 1-(4-n-Propylphenyl)-4-hydroxymethyl-2-pyrrolidone 
• 133747-75-8 methyl 1-(4-n-propylphenyl)-5-oxo-3-pyrrolidinecarboxylate 

Relevant articles and documents

Synthesis of 4-methyloxybenzoic acids and related compounds, and their inhibitory capacities toward fatty-acid and sterol biosynthesis

The synthesis of a series of 4-methyloxybenzoic acids and related compounds, and their evaluation for inhibitory capacity toward fatty-acid and sterol biosyntheses using rats' liver slices in vitro and rabbits

Phenylcarboxylic acid derivatives having hetero ring

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.