13901-76-3

Basic information

• Product Name: dimethyl 1-methyl-2,5-diphenyl-1H-pyrrole-3,4-dicarboxylate
• Synonyms: dimethyl 1-methyl-2,5-diphenyl-1H-pyrrole-3,4-dicarboxylate
• CAS NO: 13901-76-3
• Molecular Formula: C₂₁H₁₉NO₄
• Molecular Weight: 349.37986
• Mol File: 13901-76-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: dimethyl 1-methyl-2,5-diphenyl-1H-pyrrole-3,4-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 1-methyl-2,5-diphenyl-1H-pyrrole-3,4-dicarboxylate(13901-76-3)
• EPA Substance Registry System: dimethyl 1-methyl-2,5-diphenyl-1H-pyrrole-3,4-dicarboxylate(13901-76-3)

Safety Data

• Hazardous Substances Data: 13901-76-3(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 614-27-7 methyl 3-oxo-3-phenylpropionate 
• 138073-15-1 N-Methyl-N-(phenyl-trimethylsilanyl-methyl)-benzamide 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 61802-83-3 N-methyl-N-benzylbenzamide 
• 28544-45-8 N-benzoyl-N-methylphenylglycine 

Downstream Products

• 72572-67-9 (4-Hydroxymethyl-1-methyl-2,5-diphenyl-1H-pyrrol-3-yl)-methanol 

Relevant articles and documents

Electrochemical Oxidative Cyclization: Synthesis of Polysubstituted Pyrrole from Enamines

A conceptually novel method for the preparation of pyrrole is described by electrochemical-oxidation-induced intermolecular annulation via enamines. In a simple undivided cell, based on a sodium acetate-facilitated, polysubstituted pyrrole derivations has been facilely synthesized under external oxidant-free condition. This electrosynthetic approach providing an environmentally benign protocol for C?C bond cross-coupling and oxidative annulation, which features unparalleled broad scope of substrates and practicality.

Acylamino chromium carbene complexes: Direct carbonyl insertion, formation of munchnones, and trapping with dipolarophiles [7]

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THE USE OF N-ETHYL-N'-DIMETHYLAMINOPROPYLCARBODIIMIDE OR SILICON TETRACHLORIDE IN PYRROLE SYNTHESES.

Two methods are used for mesoionic oxazolone formation in the synthesis of pyrroles in 1,3-dipolar cycloaddition reactions.N-ethyl-N'-dimethylaminopropylcarbodiimide or silicon tetrachloride are used to activate the N-acylamino acid.