1376612-06-4

Basic information

• Product Name: ethyl 2-cyclopropyl-1-tosyl-2,5-dihydropyrrole-3-carboxylate
• Synonyms: ethyl 2-cyclopropyl-1-tosyl-2,5-dihydropyrrole-3-carboxylate
• CAS NO: 1376612-06-4
• Molecular Weight: 335.424
• Mol File: 1376612-06-4.mol

Chemical Properties

• CAS DataBase Reference: ethyl 2-cyclopropyl-1-tosyl-2,5-dihydropyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-cyclopropyl-1-tosyl-2,5-dihydropyrrole-3-carboxylate(1376612-06-4)
• EPA Substance Registry System: ethyl 2-cyclopropyl-1-tosyl-2,5-dihydropyrrole-3-carboxylate(1376612-06-4)

Safety Data

• Hazardous Substances Data: 1376612-06-4(Hazardous Substances Data)

Upstream product

• 39595-70-5 ethyl 3-bromoprop-1-yne-1-carboxylate 
• 1376611-80-1 ethyl 2-[cyclopropyl(hydroxy)methyl]-2,3-butadienoate 
• 1376611-87-8 3-ethoxycarbonyl-4-(tosylcarbamoyloxy)-4-cyclopropyl-1,2-butadiene 
• 1376611-95-8 3-ethoxycarbonyl-4-tosylamino-4-cyclopropyl-1,2-butadiene 

Relevant articles and documents

Phosphine-Catalyzed (4+1) Annulation: Rearrangement of Allenylic Carbamates to 3-Pyrrolines through Phosphonium Diene Intermediates

We have developed a phosphine-catalyzed (4+1) annulative rearrangement for the preparation of 3-pyrrolines from allenylic carbamates via phosphonium diene intermediates. We employed this methodology to synthesize an array of 1,3-disubstituted- and 1,2,3-t

Phosphine-catalyzed intramolecular γ-umpolung addition of α-aminoalkylallenic esters: Facile synthesis of 3-carbethoxy-2-alkyl-3- pyrrolines

An array of N-tosylated α-aminoalkylallenic esters was prepared and their cyclization under the influence of nucleophilic phosphine catalysts was explored. The α-aminoalkylallenic esters were prepared through aza-Baylis-Hillman reactions or novel DABCO-me