97336-41-9

Basic information

• Product Name: 3,4-DIETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER
• Synonyms: 1-H-ETHYL-3,4-DIETHYLPYRROLE CARBOXYLATE;3,4-DIETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER;3,4-DIETHYL-2-CARBOETHOXY-1H-PYRROLE;3,4-DIETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER 97%;Ethyl 3,4-diethyl-1H-pyrrole-2-carboxylate;2-Ethoxycarbonyl-3,4-diethylpyrrole;Ethyl 3,4-diethylpyrrole-2-carboxylate;1H-Pyrrole-2-carboxylic acid, 3,4-diethyl-, ethyl ester
• CAS NO: 97336-41-9
• Molecular Formula: C₁₁H₁₇NO₂
• Molecular Weight: 195.26
• Product Categories: pharmacetical;Porphyrins;Porphyrin Building Blocks
• Mol File: 97336-41-9.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 312℃
• Flash Point: 142℃
• Appearance: /
• Density: 1.039
• Vapor Pressure: 0.000552mmHg at 25°C
• Refractive Index: 1.51
• CAS DataBase Reference: 3,4-DIETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER(97336-41-9)
• EPA Substance Registry System: 3,4-DIETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER(97336-41-9)

Safety Data

• Hazardous Substances Data: 97336-41-9(Hazardous Substances Data)

Usage

General Description

3,4-Diethyl-1H-pyrrole-2-carboxylic acid ethyl ester is a chemical compound typically utilized in industry for research and development purposes. Its chemical formula is C12H19NO2, displaying properties related to both pyrrole and carboxylic acid ethyl ester categories of organic compounds. Pyrroles have a ring-like structure containing nitrogen, while carboxylic acid esters are often part of various common fats and oils. This substance, being an ester, is likely to exhibit characteristics like being flammable, having a fruity smell, and undergoing hydrolysis in the presence of bases or acids. The specific properties, usage, hazards, and safety measures related to this compound are usually detailed in its Material Safety Data Sheet (MSDS) provided by manufacturers or distributors.

InChI:InChI=1/C11H17NO2/c1-4-8-7-12-10(9(8)5-2)11(13)14-6-3/h7,12H,4-6H2,1-3H3

Upstream product

• 4812-22-0 2-ethyl-1-nitro-2-butene 
• 2999-46-4 Ethyl isocyanoacetate 
• 3750-83-2 4-acetoxy-3-nitrohexane 
• 67-63-0 isopropyl alcohol 
• 68216-53-5 (E)-3-nitrohex-3-ene 
• 5342-71-2 4-Nitrohexan-3-ol 
• 113999-02-3 ethyl 3,4-diethyl-5-iodo-1H-pyrrole-2-carboxylate 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Downstream Products

• 147590-65-6 2-benzyl 3,4-diethyl-1H-pyrrole-2-carboxylate 
• 16200-52-5 3,4-diethyl-1H-pyrrole 
• 865855-40-9 2,5-bis((5-benzyloxycarbonyl-3-n-butyl-4-methyl-2-pyrrolyl)methyl)-3,4-diethyl-1H-pyrrole 
• 157873-93-3 3,4-diethyl-1H-pyrrole-2-carboxylic acid 
• 34874-30-1 3,4-diethyl-2-methyl-1H-pyrrole 
• 443308-93-8 C₂₉H₃₇N₃O₆ 
• 177167-60-1 diethyl 5,5'-(phenylmethylene)bis(3,4-diethyl-1H-pyrrole-2-carboxylate) 
• 159189-64-7 1-methyl>-2-methoxybenzene 
• 159428-02-1 α-(Hydroxymethyl)-3,4-diethylpyrrole 
• 159189-61-4 1-methyl>-3,5-di-t-butylbenzene 
• 2683-82-1 2,3,7,8,12,13,17,18-octaethyl-porphyrin 
• 130274-66-7 3,4-diethyl-2,5-diformylpyrrole 
• 1006-26-4 3,4-diethylpyrrole-2-carbaldehyde 

Relevant articles and documents

BORON-CONTAINING CYCLIC EMISSIVE COMPOUNDS AND COLOR CONVERSION FILM CONTAINING THE SAME

The present disclosure relates to novel photoluminescent complexes comprising a BODIPY moiety covalently bonded to a blue light absorbing moiety, a color conversion film comprising the photoluminescent complex, and a back-light unit using the same.

Synthesis of 2,2′-bipyrrole-5-carboxaldehydes and their application in the synthesis of B-ring functionalized prodiginines and tambjamines

Facile, versatile, and cost-effective synthetic routes for the preparation of a range of new 3-alkyl-, 4-alkyl-, 3,4-dialkyl-, and 3-halo-4-alkyl-2, 2′-bipyrrole-5-carboxaldehydes have been developed. These 2,2′-bipyrrole-5-carboxaldehydes offer interesting potential as building blocks for making bioactive natural and unnatural products, as demonstrated by the synthesis of B-ring functionalized prodiginines (PGs) and tambjamines.

Meso-unsubstituted iron corrole in hemoproteins: Remarkable differences in effects on peroxidase activities between myoglobin and horseradish peroxidase

(Figure Presented) Myoglobin (Mb) and horseradish peroxidase (HRP) were both reconstituted with a meso-unsubstituted iron corrole and their electronic configurations and peroxidase activities were investigated. The appearance of the 540 nm band upon incorporation of the iron corrole into apoMb indicates axial coordination by the proximal histidine imidazole in the Mb heme pocket. Based on 1H NMR measurements using the Evans method, the total magnetic susceptibility of the iron corrole reconstituted Mb was evaluated to be S = 3/2. In contrast, although a band does not appear in the vicinity of 540 nm during reconstitution of the iron corrole into the matrix of HRP, a spectrum similar to that of the iron corrole reconstituted Mb is observed upon the addition of dithionite. This observation suggests that the oxidation state of the corrole iron in the reconstituted HRP can be assigned as +4. The catalytic activities of both proteins toward guaiacol oxidation are quite different; the iron corrole reconstituted HRP decelerates H2O2-dependent oxidation of guaiacol, while the same reaction catalyzed by iron corrole reconstituted Mb has the opposite effect and accelerates the reaction. This finding can be attributed to the difference in the oxidation states of the corrole iron when these proteins are in the resting state.