63833-46-5

Basic information

• Product Name: 1H-Pyrrole-3-carboxylic acid, 5-benzoyl-2,4-dimethyl-, ethyl ester
• CAS NO: 63833-46-5
• Molecular Formula: C16H17NO3
• Molecular Weight: 271.316
• Mol File: 63833-46-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-3-carboxylic acid, 5-benzoyl-2,4-dimethyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-3-carboxylic acid, 5-benzoyl-2,4-dimethyl-, ethyl ester(63833-46-5)
• EPA Substance Registry System: 1H-Pyrrole-3-carboxylic acid, 5-benzoyl-2,4-dimethyl-, ethyl ester(63833-46-5)

Safety Data

• Hazardous Substances Data: 63833-46-5(Hazardous Substances Data)

Upstream product

• 2199-51-1 2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 98-88-4 benzoyl chloride 
• 100-47-0 benzonitrile 
• 1468-28-6 4-benzoylmorpholine 
• 71942-15-9 N,N-dimethyl benzamide-POCl₃ complex 
• 28528-45-2 N,N'-diethyl benzamide-POCl₃ complex 
• 82106-18-1 C₁₁H₁₃Cl₂NO₃P⁽¹⁺⁾*Cl^(1-) 
• 611-74-5 N,N-dimethylbenzamide 
• 82120-51-2 α-(4-ethoxycarbonyl-3,5-dimethylpyrrol-2-yl) benzylidene-3-chloropropylamine 
• 3389-54-6 n-benzoylpyrrolidine 
• 3420-62-0 azetidin-1-yl(phenyl)methanone 
• 7556-56-1 1-benzoyl-4-methylpiperazine 
• 6797-44-0 2-oximino-1-penyl-1,3-butanedione 
• 141-97-9 ethyl acetoacetate 

Downstream Products

• 86770-48-1 ethyl 5-benzyl-2,4-dimethylpyrrole-3-carboxylate 

Relevant articles and documents

Rate Measurements of Certain Vilsmeier-Haack Reactions. Part 3. The Reactivities of Various Pyrrole Substrates

The rates of reaction of six pyrrole substrates with the Vilsmeier-Haack reagent derived from NN-dimethylbenzamide (and in some cases from N-benzoylmorpholine or NN-diethylbenzamide) and phosphoryl chloride were measured.The deactivating effect on substit

Rate Measurements of Certain Vilsmeier-Haack Reactions. Part 2. The Effect of N-Substituents in the Amide

Rate measurements on the reaction between a series of amide-POCl3 complexes (2a-h) and ethyl 2,4-dimethyl-pyrrole-3-carboxylate in 1,2-dichloroethane were used to study the effect of N-substituents in amides (1a-h) on the Vilsmeier-Haack reaction.The resu