34549-93-4

Basic information

• Product Name: 3-Ethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester
• Synonyms: 3-Ethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester;ETHYL 4,5-DIMETHYL-3-ETHYL-2-PYRROLECARBOXYLATE;ethyl 3-ethyl-4,5-dimethyl-1H-pyrrole-2-carboxylate
• CAS NO: 34549-93-4
• Molecular Formula: C₁₁H₁₇NO₂
• Molecular Weight: 195.26
• Mol File: 34549-93-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Ethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Ethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester(34549-93-4)
• EPA Substance Registry System: 3-Ethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester(34549-93-4)

Safety Data

• Hazardous Substances Data: 34549-93-4(Hazardous Substances Data)

Upstream product

• 69687-83-8 ethyl 3-ethyl-5-methyl-2-pyrrolecarboxylate 
• 4220-52-4 3-methyl-2,4-hexanedione 
• 13433-00-6 diethyl aminomalonate hydrochloride 
• 2199-45-3 4,5-dimethyl-pyrrole-2-carboxylic acid ethyl ester 
• 123-63-7 paracetaldehyde 
• 4949-44-4 ethyl propanoylacetate 
• 27093-55-6 ethyl 3-ethyl-4-t-butoxycarbonyl-5-methyl-pyrrole-2-carboxylate 
• 66414-04-8 diethyl 3-ethyl-5-methylpyrrole-2,4-carboxylate 
• 541-41-3 chloroformic acid ethyl ester 
• 100780-37-8 2-nitro-3-acetoxy-pentane 
• 161198-53-4 [1-Methylsulfanyl-eth-(E)-ylideneamino]-acetic acid ethyl ester 
• 86634-27-7 ethyl 3-ethyl-1-hydroxymethyl-4,5-dimethylpyrrole-2-carboxylate 
• 6829-41-0 diethyl oximinomalonate 
• 123-62-6 propionic acid anhydride 

Downstream Products

• 204068-74-6 2-carboxy-3-ethyl-4-methyl-pyrrole 
• 143064-86-2 benzyl 3,4-butano-5'-(tert-butoxycarbonyl)-4'-ethyl-3'-methyl-2,2'-dipyrrylmethane-5-carboxylate 
• 159152-49-5 2,5-Bis(5'-benzyloxycarbonyl-4'-ethyl-3'-methylpyrrol-2'-ylmethyl)pyrrole 
• 56015-18-0 benzyl 5-acetoxymethyl-3-ethyl-4-methylpyrrole-2-carboxylate 
• 623945-15-3 2-formyl-4-methyl-3-ethyl-5-ethynyl-1H-pyrrole 
• 61538-85-0 benzyl 3-ethyl-4,5-dimethyl-pyrrole-2-carboxylate 

Relevant articles and documents

Competing Knorr and Fischer-Fink pathways to pyrroles in neutral aqueous solution

A proposed chemical model for the prebiogenesis of tetrapyrrole macrocycles relies on the condensation of a 3-alkyl-substituted 2,4-diketone and an α-aminoketone to form a pyrrole equipped for subsequent self-condensation leading to porphyrinogens. The co

CONCERNING THE MECHANISM OF FORMATION OF BILIVERDINS FROM b-BILENES

The oxidation of 1,19-di-t-butoxycarbonyl-b-bilenes with bromine affords not only a major biliverdin, but also minor biliverdins.Elucidation of their structure revealed that cleavage of the b-bilene chain takes place during the oxidation, followed by dime

ELECTROPHILIC HETEROAROMATIC SUBSTITUTIONS. VI. THE REACTION OF SOME 3,4,5-TRI- AND 1,3,4,5-TETRASUBSTITUTED 2-METHYLPYRROLES WITH MANNICH REAGENTS

The reaction of a series of 3,4,5-tri- (1) and 1,3,4,5-tetrasubstituted (2) (2)-methylpyrroles with Mannich reagents formed in situ from a secondary aliphatic amine and formaldehyde has been investigated in aqueous acetic acid, methanol, and dioxan.No rea