4391-98-4

Basic information

• Product Name: 1H-Pyrrole-2-carboxylicacid,4-ethyl-3-methyl-,ethylester(9CI)
• Synonyms: 1H-Pyrrole-2-carboxylicacid,4-ethyl-3-methyl-,ethylester(9CI);1H-PYRROLE-2-CARBOXYLIC ACID,4-ETHYL-3-METHYL-,ETHYL ESTER(WXC08706)
• CAS NO: 4391-98-4
• Molecular Formula: C₁₀H₁₅NO₂
• Molecular Weight: 181.23
• Product Categories: PYRROLE
• Mol File: 4391-98-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrole-2-carboxylicacid,4-ethyl-3-methyl-,ethylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2-carboxylicacid,4-ethyl-3-methyl-,ethylester(9CI)(4391-98-4)
• EPA Substance Registry System: 1H-Pyrrole-2-carboxylicacid,4-ethyl-3-methyl-,ethylester(9CI)(4391-98-4)

Safety Data

• Hazardous Substances Data: 4391-98-4(Hazardous Substances Data)

Usage

Derivation

Derived from pyrrole, a five-membered aromatic heterocyclic organic compound

Use

Building block for the synthesis of various biologically active compounds in the pharmaceutical industry

Potential properties

Anti-inflammatory and anti-cancer properties

Physical properties

Colorless liquid, fruity odor, soluble in organic solvents

Safety

Handle with care and follow proper safety protocols in laboratory settings.

Upstream product

• 488-92-6 3-ethyl-4-methyl-1H-pyrrole 
• 53365-89-2 5-Ethoxycarbonyl-3-ethyl-4-methylpyrrole-2-carboxylic acid 
• 7467-77-8 diethyl 3-ethyl-4-methylpyrrole-2,5-dicarboxylate 
• 57745-28-5 Ethyl 4-ethyl-5-iodo-3-methylpyrrole-2-carboxylate 
• 2999-46-4 Ethyl isocyanoacetate 
• 89896-01-5 3-nitropentan-2-ol acetate 
• 5447-99-4 3-nitro-pentan-2-ol 
• 97336-18-0 4-Ethyl-3-methyl-5-trichloromethyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 1540-34-7 3-ethyl-2,4-pentanedione 
• 2199-47-5 ethyl 3,5-dimethyl-4-ethylpyrrole-2-carboxylate 

Downstream Products

• 856119-30-7 5-acetyl-4-ethyl-3-methyl-pyrrole-2-carboxylic acid ethyl ester 
• 23466-29-7 4-ethyl-3-methyl-pyrrole-2-carboxylic acid 
• 25553-59-7 2,5-bis(5-carboxy-3-ethyl-4-methyl-2-pyrrolylmethyl)furan 
• 190331-83-0 Diethyl 3,7-diethyl-2,8-dimethyl-5-phenyldihydrodipyrrin-1,9-dicarboxylate 
• 126380-11-8 ms-(4''-methoxyphenyl)-5,5'-dicarbethoxy-4,4'-dimethyl-3,3'-diethyldipyrrolylmethane 
• 102393-34-0 C₅₈H₇₀N₈O₄ 
• 102393-35-1 1,4-bis<5-<2-<(5-ethoxycarbonyl-3-ethyl-4-methylpyrrol-2-yl)methyl>-5-(2,2-dicyanovinyl)-4-methylpyrrol-3-yl>pentyl>-2,3,5,6-tetramethylbenzene 
• 102393-36-2 C₆₄H₈₂N₈O₄ 
• 144582-06-9 1,4-Bis<4-<2-((5-ethoxycarbonyl-3-ethyl-4-methylpyrrol-2-yl)methyl)-5-(2-cyano-2-methoxycarbonylvinyl)-4-methylpyrrol-3-yl>butyl>benzene 
• 51089-83-9 benzyl 4-ethyl-3-methyl-1H-pyrrole-2-carboxylate 
• 6305-93-7 [5,5'-bis(ethoxycarbonyl)-3,3'-diethyl-4,4'-dimethyl-2,2'-dipyrrolyl]methane 
• 988-63-6 2-<(5'-ethoxycarbonyl-3'-ethyl-4'-methylpyrrole-2-yl)methyl>-5-benzyloxycarbonyl-3-ethyl-4-methylpyrrole 
• 190331-86-3 Diethyl 3,7-diethyl-5-(4-hydroxymethylphenyl)-2,8-dimethyldihydrodipyrrin-1,9-dicarboxylate 

Relevant articles and documents

Synthesis and spectrophotometric study of acidic and complexing properties of 5,15-bis(4'-methoxyphenyl)-10,20-bis(4″-nitrophenyl)-2,8,12,18-tetramethyl-3,7,13,17-tetraethylporphyn in acetonitrile

Abstract 5,15-Bis(4'-methoxyphenyl)-10,20-bis(4″-nitrophenyl)-2,8,12,18-tetramethyl-3,7,13,17-tetraethylporphyne was synthesized and studied spectrophotometrically in the systems 1,8-diazabicyclo[5.4.0]undec-7-ene-acetonitrile, Zn(OAc)2-acetoni

Artificial photosynthetic reaction centers with carotenoid antennas

Two reaction center-antenna models based on a purpurin macrocycle linked to a C60 and to a carotenoid polyene have been synthesized. In these systems the C60 moiety is the primary electron acceptor, the purpurin is the primary electr

Deiodination of 5-iodopyrrole-2-carboxylates using sodium formate catalyzed by palladium complexes: Preparation of 5-unsubstituted pyrrole-2-carboxylates

5-Iodopyrrole-2-carboxylates are deiodinated with sodium formate in the presence of a catalytic amount of either PdCl2(Ph3P)2 or Pd(Ph3P)4 to give the corresponding 5-unsubstituted pyrrole-2-carboxyla