92634-76-9

Basic information

• Product Name: ETHYL 4-(2,5-DIOXOTETRAHYDRO-1H-PYRROL-1-YL)BENZOATE
• Synonyms: ETHYL 4-(2,5-DIOXO-1-PYRROLIDINYL)BENZENECARBOXYLATE;ETHYL 4-(2,5-DIOXOTETRAHYDRO-1H-PYRROL-1-YL)BENZOATE;N-(4-ETHOXYCARBONYLPHENYL)SUCCINIMIDE
• CAS NO: 92634-76-9
• Molecular Formula: C₁₃H₁₃NO₄
• Molecular Weight: 247.25
• Mol File: 92634-76-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 158℃
• Boiling Point: 490.3 °C at 760 mmHg
• Flash Point: 250.3 °C
• Appearance: /
• Density: 1.292g/cm³
• Vapor Pressure: 9.27E-10mmHg at 25°C
• Refractive Index: 1.573
• CAS DataBase Reference: ETHYL 4-(2,5-DIOXOTETRAHYDRO-1H-PYRROL-1-YL)BENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 4-(2,5-DIOXOTETRAHYDRO-1H-PYRROL-1-YL)BENZOATE(92634-76-9)
• EPA Substance Registry System: ETHYL 4-(2,5-DIOXOTETRAHYDRO-1H-PYRROL-1-YL)BENZOATE(92634-76-9)

Safety Data

• Safety Statements: S24/25:Avoid contact with skin and eyes.
• Hazardous Substances Data: 92634-76-9(Hazardous Substances Data)

Usage

General Description

Ethyl 4-(2,5-dioxotetrahydro-1H-pyrrol-1-yl)benzoate is a chemical compound that belongs to the class of esters. It is commonly used in the pharmaceutical industry as an intermediate for the synthesis of various drugs. ETHYL 4-(2,5-DIOXOTETRAHYDRO-1H-PYRROL-1-YL)BENZOATE has potential therapeutic applications due to its structural properties, which make it suitable for further modification to develop new pharmaceutical products. Additionally, it may also have uses in academic research and chemical synthesis due to its unique chemical structure and reactivity. Overall, ethyl 4-(2,5-dioxotetrahydro-1H-pyrrol-1-yl)benzoate is an important chemical with diverse potential applications in various fields.

InChI:InChI=1/C13H13NO4/c1-2-18-13(17)9-3-5-10(6-4-9)14-11(15)7-8-12(14)16/h3-6H,2,7-8H2,1H3

Upstream product

• 110-15-6 succinic acid 
• 94-09-7 p-aminoethylbenzoate 
• 108-30-5 succinic acid anhydride 

Relevant articles and documents

Design of branched and chiral solvatochromic probes: Toward quantifying polarity gradients in dendritic macromolecules

(Chemical Equation Presented) A pair of chiral, branched monomer building blocks, consisting of a solvatochromic probe and a spectroscopically inactive volume dummy, has been developed. The probe can selectively be excited, and its fluorescence characteristics provide information about local polarity. Incorporation of these monomers into high-generation polyester dendrimers should enable a detailed investigation of the polarity/density profile in dendritic architectures and ultimately allow for the realization of energy gradients from one chromophore building block only.