28168-20-9

Basic information

• Product Name: 2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid methyl ester
• Synonyms: 2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid methyl ester
• CAS NO: 28168-20-9
• Molecular Weight: 215.252
• Mol File: 28168-20-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid methyl ester(28168-20-9)
• EPA Substance Registry System: 2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid methyl ester(28168-20-9)

Safety Data

• Hazardous Substances Data: 28168-20-9(Hazardous Substances Data)

Upstream product

• 105-45-3 acetoacetic acid methyl ester 
• 70-11-1 α-bromoacetophenone 
• 536-74-3 phenylacetylene 
• 14205-39-1 methyl 3-aminocrotonate 
• 75519-84-5 3-oxo-2-(2-oxo-2-phenyl-ethyl)-butyric acid methyl ester 

Relevant articles and documents

Green multicomponent reaction for synthesis of trisubstituted pyrroles in ionic liquid [bmim]BF4

2,4,5-Trisubstituted pyrrole derivatives were efficiently synthesized by one-pot condensation of 1,3-diones, α-bromoacetophenones, and ammonium acetate in ionic liquid [bmim]BF4. The new synthetic method offers multisubstituted pyrroles with th

Microwave-assisted facile synthesis of trisubstituted pyrrole derivatives

We report efficient synthesis of pyrrole derivatives by use of microwave irradiation. Quantitative yields were obtained in short reaction times. Low yields of product were obtained from alicyclic amino unsaturated ketone derivatives; higher yields were ob

Synthesis of substituted pyrroles from N-vinylic phosphazenes derived from β-amino acids and α-bromo ketones

Synthesis of di-, tri- and tetrasubstituted pyrroles by reaction of Nvinylic phosphazenes derived from β-amino acids with α-bromo ketones is described.