40236-19-9

Usage

Uses

Used in Fragrance Industry:
Benzyl 3,5-dimethylpyrrole-2-carboxylate is used as a fragrance ingredient in perfumes and personal care products due to its pleasant aroma.
Used in Pharmaceutical Industry:
Benzyl 3,5-dimethylpyrrole-2-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals.
Used in Agrochemical Industry:
Benzyl 3,5-dimethylpyrrole-2-carboxylate is used as an intermediate in the production of various agrochemicals.
Used in Organic Chemistry:
Benzyl 3,5-dimethylpyrrole-2-carboxylate is used as a versatile building block in organic chemistry due to its reactivity and ability to undergo various chemical reactions.

Upstream product

• 2199-44-2 3,5-dimethyl-2-ethoxycarbonyl-1H-pyrrole 
• 100-51-6 benzyl alcohol 
• 20194-18-7 sodium phenyl-methanolate 
• 2386-27-8 benzyl 4-acetyl-3,5-dimethylpyrrole-2-carboxylate 
• 96246-81-0 benzyl 5-dithioacetal-3-methylpyrrole-2-carboxylate 
• 123-54-6 acetylacetone 

Downstream Products

• 124307-91-1 benzyl 5-acetoxymethyl-3-methylpyrrole-2-carboxylate 
• 78829-37-5 benzyl 4-<<1-¹³C>acetyl>-3,5-dimethylpyrrole-2-carboxylate 
• 112673-93-5 4-Decanoyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 4513-93-3 3,5-dimethylpyrrole-2-carboxylic acid 
• 94781-44-9 5-Formyl-3-methyl-1H-pyrrol-2-carbonsaeure-benzylester 
• 110995-42-1 benzyl 4-<(13C)formyl>-3,5-dimethylpyrrole-2-carboxylate 
• 184775-08-4 benzyl 4-(1-hydroxy-2,2,2-trifluoroethyl)-3,5-dimethylpyrrole-2-carboxylate 
• 68500-80-1 4,4'-methylenebis[3,5-dimethyl-bis(phenymlemthyl)ester]-1H-pyrrole-2-carboxylate 
• 205492-38-2 benzyl 3,5-dimethyl-4-(trifluoroacetyl)pyrrole-2-carboxylate 
• 936016-12-5 4-(3-ethoxycarbonyl-propanoyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 936016-13-6 4-(5-ethoxycarbonyl-pentanoyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 205492-41-7 benzyl 3,5-dimethyl-4-((R)-2,2,2-trifluoro-1-hydroxyethyl)pyrrole-2-carboxylate 
• 205492-40-6 benzyl (S)-4-(1-hydroxy-2,2,2-trifluoroethyl)-3,5-dimethylpyrrole-2-carboxylate 

Relevant academic research and scientific papers

Microwave-accelerated synthesis of benzyl 3,5-dimethyl-pyrrole-2- carboxylate

Benzyl 3,5-dimethyl-pyrrole-2-carboxylate, a very useful pyrrole in porphyrin and dipyrromethene synthesis, can be synthesized via the Knorr-type reaction, but in low yield. Alternative routes to benzyl 3,5-dimethyl-pyrrole-2- carboxylate have been develo

Total Synthesis of (+/-)-Bonellin Dimethyl Ester

Bonellin (1) is the green sex-differentiating pigment of Bonellia viridis, a marine animal widely distributed in the Mediterranean Sea.Bonellin dimethylester (rac-2), has been synthesized from the four monocyclic building blocks 6, 7, 8b, 10 and the selectively cleavable malonic ester 9 by an highly convergent synthetic concept. Key Words: Bonellin / Total synthesis / Bonellia virids

Oxygen- and Carbon Monoxide-binding to a Lipophilic Diporphyrinatocopperiron Complex Solubilized in an Aqueous Medium with a Micelle

A tetradecyl-substituted diporphyrinatocopperiron complex was synthesized and solubilized in an aqueous medium with a surfactant.Both the oxygen- and carbon monoxide-binding rate constants decreased due to the steric hindrance of the porphyrinatocopper cap, which brought about a reduced gas-binding affinity in comparison with other synthetic porphyrinatoiron complexes.

Novel Porphyrins from Copper(II)-Mediated Cyclizations of 1',8'-Dimethyl-a,c-biladiene Salts: Mechanism of the Cyclization Reaction

Copper(II)-mediated cyclizations of the 1',8'-dimethyl-a,c-biladiene 8 under various conditions afford the expected porphyrin 7, along with γ-methyl- (9), γ-(dialkylamino)- (10 and 11), 6-formyl- (12), and γ-formylporphyrins (13).Carbon-13-enriched a,c-bi

Biosynthesis of Porphyrins and Related Macrocycles. Part 25. Synthesis of Analogues of Coproporphyrinogen-III and Studies of their Interaction with Copropophyrinogen-III Oxidase from Euglena gracilis

Analogues of coproporphyrinogen-III have been synthesized in which the propionate groups respectively on ring-A and on ring-B are modified either by homologation or esterification.Coproporphyrinogen-III oxidase from Euglena gracilis acts on the analogues which possess normal substituents on ring-A to generate a vinyl group on that ring.The enzyme does not affect the analogues in which the ring-A propionate group has been changed.Conditions have been defined for the MacDonald synthesis of porphyrins which yield products of high isomeric purity.

Protiodeacetylation of Porphyrins and Pyrroles: A New Partial Synthesis of Dehydrocoproporphyrin (S411-Porphyrin)

Treatment of copper(II) complexes of acetylporphyrins with ethanedithiol and boron trifluoride-ether in acetic acid efficiently accomplishes deacetylation of the porphyrin system, and this reaction is demonstrated in a new partial synthesis of dehydrocopr