40236-19-9

Basic information

• Product Name: Benzyl 3,5-dimethylpyrrole-2-carboxylate
• Synonyms: Benzyl 3,5-dimethylpyrrole-2-carboxylate;Benzyl 3.5-diMethyl-1H-pyrrole-2-carboxylate;3,5-DIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID BENZYL ESTER
• CAS NO: 40236-19-9
• Molecular Formula: C₁₄H₁₅NO₂
• Molecular Weight: 229.2744
• Mol File: 40236-19-9.mol
• Article Data: 7

Chemical Properties

• Melting Point: 102 °C
• Boiling Point: 378.9±37.0 °C(Predicted)
• Appearance: /
• Density: 1.152±0.06 g/cm3(Predicted)
• PKA: 16.10±0.50(Predicted)
• CAS DataBase Reference: Benzyl 3,5-dimethylpyrrole-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 3,5-dimethylpyrrole-2-carboxylate(40236-19-9)
• EPA Substance Registry System: Benzyl 3,5-dimethylpyrrole-2-carboxylate(40236-19-9)

Safety Data

• Hazardous Substances Data: 40236-19-9(Hazardous Substances Data)

Usage

General Description

Benzyl 3,5-dimethylpyrrole-2-carboxylate is a chemical compound with the molecular formula C14H15NO2. It is a pyrrole derivative that is commonly used in the synthesis of pharmaceuticals, agrochemicals, and fragrances. Benzyl 3,5-dimethylpyrrole-2-carboxylate is known for its pleasant aroma and is often used as a fragrance ingredient in perfumes and personal care products. It is also used as an intermediate in the production of various organic compounds. Benzyl 3,5-dimethylpyrrole-2-carboxylate is considered to be 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 
• 123-54-6 acetylacetone 
• 96246-81-0 benzyl 5-dithioacetal-3-methylpyrrole-2-carboxylate 
• 2386-27-8 benzyl 4-acetyl-3,5-dimethylpyrrole-2-carboxylate 

Downstream Products

• 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 
• 124307-91-1 benzyl 5-acetoxymethyl-3-methylpyrrole-2-carboxylate 
• 205492-38-2 benzyl 3,5-dimethyl-4-(trifluoroacetyl)pyrrole-2-carboxylate 
• 1128077-13-3 C₂₄H₃₅NO₂S 
• 1128077-11-1 C₁₆H₁₉NO₂S 
• 1128077-06-4 C₂₀H₁₉NO₂S 
• 1128077-16-6 C₂₁H₂₁NO₃S 
• 184775-17-5 dibenzyl 3,4'-bis(2,2,2-trifluoro-1-methoxyethyl)-4,3'-dimethyl-2,2'-dipyrrylmethane-5,5'-dicarboxylate 
• 184775-10-8 2-benzyloxycarbonyl-3-methyl-4-(2,2,2-trifluoro-1-methoxyethyl)pyrrole-5-carboxylic acid 
• 184775-11-9 3-Methyl-4-(2,2,2-trifluoro-1-methoxy-ethyl)-1H-pyrrole-2,5-dicarboxylic acid 2-benzyl ester 5-methyl ester 
• 184775-16-4 5-Acetoxymethyl-3-methyl-4-(2,2,2-trifluoro-1-methoxy-ethyl)-1H-pyrrole-2-carboxylic acid benzyl ester 

Relevant articles and documents

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

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.

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.